Uncategorized | Visit Sedona Soon\nCheryl Anderson column: Feed My Starving Children also packs spiritual nourishment – Appleton Post Crescent\nCheryl Anderson column: Feed My Starving Children also packs spiritual nourishmentAppleton Post CrescentFinancial donations can be made at www.felc.com or by calling Jean Monson at 920-733-2303, ext. 322. Volunteers are needed for an upcoming potato Mo...\nBy spiritual - Google News|2011-07-16T02:26:11-07:00July 16th, 2011|Uncategorized|0 Comments\nBlessed With a Dark Turn of Mind: Gillian Welch’s Spiritual Strivings – Religion Dispatches\nBlessed With a Dark Turn of Mind: Gillian Welch's Spiritual StrivingsReligion DispatchesWelch's southern characters, though, emerge not from some imaginary version of God, country, and family, but from the spiritual strivings of folk who have s...\nBy spiritual - Google News|2011-07-07T14:58:47-07:00July 7th, 2011|Uncategorized|Comments Off on Blessed With a Dark Turn of Mind: Gillian Welch’s Spiritual Strivings – Religion Dispatches\nSpiritual care given to chronically ill Kentuckians – Louisville Courier-Journal\nSpiritual care given to chronically ill KentuckiansLouisville Courier-JournalThe group of 11 gathered on a pristine Saturday morning in May, with the Abbey of Gethsemani's bells ringing in the background, to address another common challenge â€” how...\nBy spiritual - Google News|2011-07-04T16:29:18-07:00July 4th, 2011|Uncategorized|Comments Off on Spiritual care given to chronically ill Kentuckians – Louisville Courier-Journal\nBurkes: Our spiritual strength originates from God – Springfield News-Leader\nBurkes: Our spiritual strength originates from GodSpringfield News-Leader11:00 pm Archie's Lounge, 1817 E. Grand St., 864-4109: Sam-A-Lama, 9 pm-1 am- 11:00 pm As a chaplain in the Air National Guard, I often will ask airmen facing difficult situat...\nBy spiritual - Google News|2011-07-02T01:02:20-07:00July 2nd, 2011|Uncategorized|Comments Off on Burkes: Our spiritual strength originates from God – Springfield News-Leader\nFaith Perspective column: Spiritual cleansing brings clarity – Green Bay Press Gazette\nFaith Perspective column: Spiritual cleansing brings clarityGreen Bay Press GazetteWhen we do, we realize how distorted our spiritual vision really is and begin to see much more clearly. In 2008, there were a string of suicides after the economic meltd...\nBy spiritual - Google News|2011-06-24T03:25:17-07:00June 24th, 2011|Uncategorized|Comments Off on Faith Perspective column: Spiritual cleansing brings clarity – Green Bay Press Gazette\nJodie Foster discusses ‘spiritual crisis’ – Musicrooms.net\nJodie Foster discusses 'spiritual crisis'Musicrooms.netMaking movies about people in spiritual crises helps me to come to terms with my own spiritual crisis. My way of organising my feelings is to make movies out of them and see problems from a...\nBy spiritual - Google News|2011-06-15T03:37:42-07:00June 15th, 2011|Uncategorized|Comments Off on Jodie Foster discusses ‘spiritual crisis’ – Musicrooms.net\nThe Power of Soul: Dr. Zhi Gang Sha discusses healing our own bodies – ABC15.com (KNXV-TV)\nThe Power of Soul: Dr. Zhi Gang Sha discusses healing our own bodiesABC15.com (KNXV-TV)It's not the 70's version with bell bottoms and lava lamps, but the Chinese medicine meets Spiritual Enlightenment kind. Sha says by healing our soul, we hea...\nBy spiritual - Google News|2011-06-14T15:24:03-07:00June 14th, 2011|Uncategorized|Comments Off on The Power of Soul: Dr. Zhi Gang Sha discusses healing our own bodies – ABC15.com (KNXV-TV)\nChorale’s performance pays tribute to spirituals – The News Journal\nChorale's performance pays tribute to spiritualsThe News JournalThe HildaMan Chorale, whose primary goal is preserving the Negro spiritual, performs at PS du Pont Middle School on Sunday night. / Special to The News Journal/SAQUAN STIMPSON Long bef...\nBy spiritual - Google News|2011-06-13T00:59:35-07:00June 13th, 2011|Uncategorized|Comments Off on Chorale’s performance pays tribute to spirituals – The News Journal\nFriends mourn loss of spiritual leader – Southeast Sun\nFriends mourn loss of spiritual leaderSoutheast SunFormer Enterprise First Baptist Church pastor Dr. Frank Wells, better known as â€œBrother Wellsâ€ died Saturday at Medical Center Enterprise. He was 78. Words like friend, mentor, brother, encourager,...\nBy spiritual - Google News|2011-06-07T15:40:21-07:00June 7th, 2011|Uncategorized|Comments Off on Friends mourn loss of spiritual leader – Southeast Sun\nFIRST-PERSON: Spiritual disciplines of effective Sunday School leaders – BP News\nFIRST-PERSON: Spiritual disciplines of effective Sunday School leaders\n(BP)--When it comes to maintaining a vital relationship with the Lord, Sunday School leaders never graduate from the spiritual disciplines prescribed ...\nBy spiritual - Google News|2009-10-14T14:02:53-07:00October 14th, 2009|Uncategorized|Comments Off on FIRST-PERSON: Spiritual disciplines of effective Sunday School leaders – BP News


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#6 29-12-2018 10:07:15\nite soccer power and a microphone\ned," Leach told the AP. "Just because you have influence, power and a microphone in front of you doesn't mean that your son should have any more right to play than the other guys."\nPITTSBURGH -- In a stunning development that no one in the NFL expected, t.Aliexpressite e Tampa Bay Buccaneers fired Super Bowl-winning coach Jon Gruden late Friday afternoon. And in what could be even more of shock, the Bucs plan to replace Gruden with Raheem Morris, who has never b.ite soccer een anything more than a position coach in any of his six seasons in the league, SI learned Friday night.Morris, whose ascension up the NFL ladder rivals another former secondary coach -- Pittsburgh'.ite soccer store 's Mike Tomlin, who has the Steelers one win away from the Super Bowl -- will probably be named the Bucs' new head coach Saturday, a source said.Morris, 32, who last month replaced Monte Kiffin\nreflects Michigan values. And if somebody's looking at it as a way station to move elsewhere, that's not our guy."The search process actually began more than two months ago,\n#7 21-01-2019 05:07:44\nIn this article, only minimum details are shared in this article.


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“A Quick Look at Luxembourg” / Chinese\n“A Quick Look at Luxembourg” with subtitles in Chinese showing a general picture of Luxembourg with cosmopolitan young people!\nPromotional video clip of the Grand Duchy of Luxembourg: work, life & leisure.\nLuxembourg, truly good (part 1 / 3)\nMarja-Leena Junker is an actress and a director of Finnish origin who has been living in Luxembourg for 30 years. She has been manager of the Théâtre du Centaure in Luxembourg for years. In this video testimonial she talks\nMiikka Heinonen is a professional photographer who's set up shop in Luxembourg. In this video testimonial, he talks about artistic freedom and the power of networking in Luxembourg.\nSanna van Look-Peltonen\nSanna van Look-Peltonen is a Finnish businesswoman living in Luxembourg for years. Listen to her talk about how easy it is to set up a business and start a family in Luxembourg.\nLife & Leisure - Studies\nHeidi Flinkman is an IT student at the University of Luxembourg. In this video testimonial she relates about her studies and socialising in Luxembourg.\nLife & Leisure - Finance & Economy - Research\nThere is a little piece of Luxembourg everywhere from city skylines to cars and even in space. Giant high strength steel beams – the kinds used in the new Freedom Towers in New York -- are produced in Luxembourg. The advanced architectural\nPromotional vidéo clip of the Grand Duchy of Luxembourg.\nLuxembourg for Finance, the agency for the development of the financial centre, has drawn inspiration from the X of the Luxembourg Signature for its latest international campaign. We Connect Europe, the world, capital markets, banks, investment funds, insurance, innovators, investors\nLuxembourg's space saga as seen through the eyes of a little girl who, like the female hero of Interstellar, becomes a brilliant space physicist... the film stems from the imagination of Grig Richters, the bubbling cofounder of Asteroid Day


DIARY OF A CLOTHESHORSE: MUST SEE - Idris Elba Covers the August 2017 Issue of Essence Magazine\nMUST SEE - Idris Elba Covers the August 2017 Issue of Essence Magazine\nNot much to say apart from great spread and video and for de ladies a topless shot ... the only thing left to say is Your Welcome!!!\nthere should be a video below of him shirtless let me know if you can see it......\nIdris get another cover this month ...... esquire..... but no one is singing and dancing or there's no fan fare...... this has happened to me before ... no fanfare also but I was up against two other bloggers who as the press mentioned were the first bloggers to get a cover ... I got two that month and my name was not mentioned\n#TUMBLEWEED but I don't have the British "fashion" industry backing me but that's all good I know one thing ..... I got European covers and more importantly I own more houses than they do and I pay for all my own shit!\nPosted by Leroy Dawkins at 03:17


The Luxembourg Green Exchange opens up to SRI funds – ABBL\nSociété de la Bourse de Luxembourg S.A. Published 03.05.2018\nAt launch, LGX displays 11 SRI funds, managed by five fund managers: Humanis Gestion d’Actifs, Luxembourg Microfinance and Development Fund, NN Investment Partners, Selectra and Sparinvest. LGX fund window’s goal is to capture and display all ESG, green and social funds recognised by leading fund labelling organisations and to provide investors with the highest level of transparency.


EvoShield Junior XVT Scion Baseball Batting Helmet, Kids, L/XL, Blue\nHome / Baseball & Softball Batting Helmets / Evoshield Batting Helmets / EvoShield Junior XVT Scion Baseball Batting Helmet, Kids, L/XL, Blue\nSKU: 4963900127498288 Categories: Baseball & Softball Batting Helmets, Evoshield Batting Helmets\nDeveloped with compression molded ear pods that are outfitted with comfort foam, the 2020 EvoShield® Youth XVT™ Scion Batting Helmet provides players with a premium, cushioned feel as they remain protected at the plate. This model of the Scion also comes equipped with a variety of ventilation holes along the sides and rear of the helmet for consistent airflow, and has a semi-gloss finish for a bold look. Dynamic Protection and Fit Compression molded foam padding with fully wrapped ear pads for a sleek, cushioned fit Ventilation ports along the sides and rear of the helmet maintain consistent airflow to keep you comfortable Low profile shell for superior fit Sizing Details: S/M: Fits hat sizes 6 – 6-1/2 L/XL: Fits hat sizes 6-1/2 – 7 Additional Details Semi-gloss finish Meets NOCSAE® Applicable standard\nRawlings Mach Gloss Senior Batting Helmet | Scarlet\nMizuno Senior B6 Two-Tone Baseball Batting Helmet, Gray


video games Archives - theaokaylife.com\nMortal Kombat X Officially Announced – See Trailer Here!\nJune 2, 2014 juzarraga\tLeave a comment\nIt looks like the bone-cracking violence that made Mortal Kombat a hit in the 1990s is making a comeback, this time with Mortal Kombat X for Xbox One and PlayStation 4. Continue reading Mortal Kombat X Officially Announced – See Trailer Here! →\n360gamingkombatmortalplaystation 3video gamesxxbox


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Cheap flights from Altoona to Luxembourg City\nCheap flights from Altoona to Luxembourg City\nChoose between BoutiqueAir, Delta Air Lines, or KLM Royal Dutch Airlines to find the best price\nCheap one-way trips starting from $ 275 from Altoona AOO to Luxembourg City LUX\nAltoona–Blair CountyLuxembourg Train Station\nCheap round trips starting from $ 593 from Altoona AOO to Luxembourg City LUX\nTravelers usually depart from Altoona–Blair County, or Altoona, PA station when they travel from Altoona to Luxembourg City. Book your trip to arrive at Luxembourg, Luxembourg Train Station, LUXEMBOURG - P&R Bouillon , or Luxembourg - Gasperich. The most popular airlines for this route are BoutiqueAir, Delta Air Lines, KLM Royal Dutch Airlines, United Airlines, and Luxair. Altoona and Luxembourg City have 137 direct flights per week.\nNumber of flights 14 13 27 36 - 24 23\nCheck-in for a flight from Altoona to Luxembourg City\nTravelers frequently search for route combinations, such as Luxembourg City and Adolfo Suárez Madrid–Barajas, Lisbon Portela, Dublin, Vienna International Airport, Milan–Malpensa, Venice Marco Polo, Munich, Porto, John Paul II International Airport Kraków–Balice, Cristiano Ronaldo International, Montpellier–Méditerranée.\nThe main airport in Luxembourg City is Luxembourg. It is also served by Frankfurt International Airport, Brussels, Düsseldorf International Airport, Brussels South Charleroi, Dortmund, Luxembourg, Stuttgart, EuroAirport Basel Mulhouse Freiburg, Cologne Bonn Airport, Eindhoven.\nIs it possible to combine flights, buses, and trains in one itinerary when traveling between Altoona and Luxembourg City?\nWhich airlines fly between Altoona and Luxembourg City?\nWhen's the best time to travel between Altoona and Luxembourg City?\nWhat flights operate between Altoona and Luxembourg City?\nWhat time do nonstop (direct) flights between Altoona and Luxembourg City depart?\nWhat time do nonstop (direct) flights between Altoona and Luxembourg City arrive?\nWhat time do flights between Altoona and Luxembourg City depart?\nWhat time do flights between Altoona and Luxembourg City arrive?\nFlights from Milan–Malpensa to Luxembourg City\nFlights from John Paul II International Airport Kraków–Balice to Luxembourg City\nFlights from Montpellier–Méditerranée to Luxembourg City\nFind the best connection from Altoona to Luxembourg City


P. Roser, M. J. Schmidt, M. Drescher and D. Summerer\nWe here review strategies for site-directed spin labeling (SDSL) of proteins and discuss their potential for EPR distance measurements to study protein function in vitro and in cells.\nOrg. Biomol. Chem., 2016,14, 5468-5476\nChad N. Ungarean, Emma H. Southgate and David Sarlah\nA comprehensive review covering the field of enantioselective polyene cyclizations.\nOrg. Biomol. Chem., 2016,14, 5454-5467\nDiverse bioorthogonal reactions and chemical tagging approaches for protein labeling are discussed and compared in this review.\nOrg. Biomol. Chem., 2016,14, 5417-5439\nRecent developments in synthetic methods for benzo[b]heteroles\nBin Wu and Naohiko Yoshikai\nThis review summarizes recent developments in synthetic methods for benzoheterole compounds of significant potential for applications in materials science.\nOrg. Biomol. Chem., 2016,14, 5402-5416\nA review of the isolation, biological activity, biosynthesis and chemical synthesis of nitropyrrole-containing natural products reported to date, including the pyrrolomycins, heronapyrroles and nitropyrrolins.\nOrg. Biomol. Chem., 2016,14, 5390-5401\nTrihaloethenes as versatile building blocks for organic synthesis\nAdriana S. Grossmann and Thomas Magauer\nTrihaloethenes are versatile C2-building blocks that can be simply modified via addition, elimination and transition metal-catalyzed reactions.\nOrg. Biomol. Chem., 2016,14, 5377-5389\nThis review highlights the use of the oxidative boron Heck reaction in enantioselective Heck-type couplings.\nOrg. Biomol. Chem., 2016,14, 5357-5366\nVictoria K. Kensy, Gregory I. Peterson, Derek C. Church, Neal A. Yakelis and Andrew J. Boydston\nWe have investigated the dynamic nature of 1,2-oxazines, which revealed broad tunability and potential for applications in covalent adaptable materials.\nOrg. Biomol. Chem., 2016,14, 5617-5621\nAnup Bhunia, Santhivardhana Reddy Yetra, Rajesh G. Gonnade and Akkattu T. Biju\nThe K3PO4-mediated intramolecular Rauhut-Currier type reaction of chalcones having an enoate moiety leading to the formation of 4H-chromenes in moderate to good yields is demonstrated.\nMarcel Best, Isabel Porth, Sebastian Hauke, Felix Braun, Dirk-Peter Herten and Richard Wombacher\nA small synthetic calcium sensor that can be site-specifically coupled to any protein of interest in living cells by utilizing the bio-orthogonal HaloTag labeling strategy.\nOrg. Biomol. Chem., 2016,14, 5606-5611\nTotal synthesis of three important trehalose containing tetrasaccharides isolated from Mycobacterium smegmatis is reported for the first time, using regioselective opening of benzylidene acetals and stereoselective glycosylations as key steps.\nOrg. Biomol. Chem., 2016,14, 5595-5598\nFacile synthesis of enantioenriched phenol-sulfoxides and their aluminum complexes\nYani Tang, Yuji Sun, Jiyong Liu and Simon Duttwyler\nChiral phenolic p-tolylsulfoxides, t-butylsulfoxides and well-defined aluminum complexes were prepared by short synthetic routes from readily available starting materials.\nOrg. Biomol. Chem., 2016,14, 5580-5585\nStereoselective synthesis of thiazino[4,3-a]indoles using the thia-Pictet–Spengler reaction of indoles bearing N-tethered thiols and vinylogous thiocarbonates\nSantosh J. Gharpure and Santosh K. Nanda\nThia-Pictet–Spengler cyclization is used for stereoselective synthesis of N-fused thiazinoindole derivatives. One-pot, sequential Friedel–Crafts alkylation – Pictet–Spengler cyclization and the synthesis of thiazino-oxepino-indole is developed.\nOrg. Biomol. Chem., 2016,14, 5586-5590\nXiaowen Yang, Dimin Wu, Zhaohong Lu, Hongbin Sun and Ang Li\nWe report herein a protocol for preparing alkynes from alkenyl triflates at ambient temperature with LiCl as a promoter.\nHendrik Frisch, Daniel Spitzer, Mathias Haase, Thomas Basché, Jens Voskuhl and Pol Besenius\nThe synthesis and self-assembly of a new C2-symmetric oligohistidine amphiphile equipped with an aggregation induced emission luminophore is reported.\nSudam Ganpat Dawande, Bapurao Sudam Lad, Sunitkumar Prajapati and Sreenivas Katukojvala\nA new rhodium-catalyzed [4 + 2]-pyridannulation of 3-substituted indoles with diazoenals resulted in the biologically important pyrido[1,2-a]indoles.\nOrg. Biomol. Chem., 2016,14, 5569-5573\nDescribed herein a divergent strategy for the synthesis of furo[3,4-b]indoles via a sequential Ag(I)/Bi(III)/Pd(II) catalysis and cyclopenta[b]indoles via a one-pot Ag(I)/Brønsted acid relay catalysis, starting from the easily accessible 3-(2 aminophenyl)-4-pentenyn-3-ols.\nOrg. Biomol. Chem., 2016,14, 5563-5568\nSynthesis of 2-diphospho-myo-inositol 1,3,4,5,6-pentakisphosphate and a photocaged analogue\nI. Pavlovic, D. T. Thakor and H. J. Jessen\nDiphosphoinositol polyphosphates (inositol pyrophosphates, X-InsP7) are a family of second messengers with important roles in eukaryotic biology. A new approach targeting 2-InsP7 and a photocaged analogue is described.\nOrg. Biomol. Chem., 2016,14, 5559-5562\nRuthenium photoredox-triggered phospholipid membrane formation\nM. D. Hardy, D. Konetski, C. N. Bowman and N. K. Devaraj\nAs more methodologies for generating and manipulating biomimetic cellular systems are developed, opportunities arise for combining different methods to create more complex synthetic biological constructs.\nOrg. Biomol. Chem., 2016,14, 5555-5558\nThe efficient conversion of siphonodictyal B into the spirocyclic natural products corallidictyals A–D has been achieved via oxidative and acid catalyzed cyclizations.\nOrg. Biomol. Chem., 2016,14, 5546-5549\nN-Heterocyclic carbene catalysed 1,6-hydrophosphonylation of p-quinone methides and fuchsones: an atom economical route to unsymmetrical diaryl- and triarylmethyl phosphonates\nPanjab Arde and Ramasamy Vijaya Anand\nA direct method for the synthesis of diaryl- and triarylmethyl phosphonates through 1,6-hydrophosphonylation of p-quinone methides and fuchsones using NHC as a Brønsted base catalyst is described.\nOrg. Biomol. Chem., 2016,14, 5550-5554\nCedric J. Stress, Pascal J. Schmidt and Dennis. G. Gillingham\nWe use kinetic data, photophysical properties, and mechanistic analyses to compare recently developed high-rate constant oxime and hydrazone formations.\nOrg. Biomol. Chem., 2016,14, 5529-5533\n3-Component synthesis of α-substituted sulfonamides via Brønsted acid-catalyzed C(sp3)–H bond functionalization of 2-alkylazaarenes\nT. Beisel, J. Kirchner, T. Kaehler, J. Knauer, Y. Soltani and G. Manolikakes\nA Brønsted acid-catalyzed addition of 2-alkylazaarenes to in situ generated N-sulfonylimines through selective C(sp3)–H bond functionalization has been developed.\nOrg. Biomol. Chem., 2016,14, 5525-5528\nIn this report, we describe an efficient way to generate libraries of macrocyclic glycopeptides in one step by reacting phage-displayed libraries of peptides with dichloro-oxime derivatives.\nOrg. Biomol. Chem., 2016,14, 5539-5545\nA. H. St. Amant, C. P. Frazier, B. Newmeyer, K. R. Fruehauf and J. Read de Alaniz\nA one-pot synthesis of anilines and nitrosobenzenes from phenols has been developed using an ipso-oxidative aromatic substitution (iSOAr) process.\nOrg. Biomol. Chem., 2016,14, 5520-5524\nFluorine-directed 1,2-trans glycosylation of rare sugars\nNuria Aiguabella, Mareike C. Holland and Ryan Gilmour\nTo reconcile the urgent need to access well defined β-configured 2,6-di-deoxypyranose analogues for chemical biology, with the intrinsic α-selectivity of the native system, the directing role of fluorine at C2 has been explored.\nOrg. Biomol. Chem., 2016,14, 5534-5538\nXuekai Zhang, Gang He and Gong Chen\nAn efficient protocol for palladium-catalyzed PE auxiliary-directed C(sp3)–H arylation reaction with sterically hindered aryl iodides was developed.\nOrg. Biomol. Chem., 2016,14, 5511-5515\nJi-Min Yang, Yan Cai, Shou-Fei Zhu and Qi-Lin Zhou\nOrg. Biomol. Chem., 2016,14, 5516-5519\nA novel Mcl-1 inhibitor chemotype based on a tetrahydroquinoline carboxylic acid was developed utilizing structure-based design, which was subsequently validated by a fluorescence polarization competition assay and HSQC NMR analysis.\nOrg. Biomol. Chem., 2016,14, 5505-5510\nRawal's catalyst as an effective stimulant for the highly asymmetric Michael addition of β-keto esters to functionally rich nitro-olefins\nA. Suresh Kumar, T. Prabhakar Reddy, R. Madhavachary and Dhevalapally B. Ramachary\nA general approach to the asymmetric synthesis of highly substituted dihydroquinolines was achieved through neighboring ortho-amino group engaged sequential Michael/amination/dehydration reactions.\nOrg. Biomol. Chem., 2016,14, 5494-5499\nIron-catalyzed transfer hydrogenation of imines assisted by an iron-based Lewis acid\nHui-Jie Pan, Teng Wei Ng and Yu Zhao\nAn iron-catalyzed transfer hydrogenation of N-aryl and N-alkyl imines using isopropanol as the hydrogen donor is reported for the first time.\nOrg. Biomol. Chem., 2016,14, 5490-5493\nE. M. Rigsbee, C. Zhou, C. M. Rasik, A. Z. Spitz, A. J. Nichols and M. K. Brown\nA method for the [2 + 2] cycloaddition of aryl ketenes and alkenes is presented.\nOrg. Biomol. Chem., 2016,14, 5477-5480\nExpedient synthesis of densely substituted pyrrolo[1,2-a]indoles\nDattatraya H. Dethe and Raghavender Boda\nThe strategy was further applied for the synthesis of optically active pyrrolo[1,2-a]indoles in >97% de using the chiral auxiliary based approach.\nOrg. Biomol. Chem., 2016,14, 5843-5860\nA clickable UTP analog for the posttranscriptional chemical labeling and imaging of RNA\nAnupam A. Sawant, Progya P. Mukherjee, Rahul K. Jangid, Sanjeev Galande and Seergazhi G. Srivatsan\nA multipurpose UTP analog potentially suitable for RNA aptamer selection and two-channel visualization of RNA in cells by using click chemistry and Raman spectroscopy has been developed.\nOrg. Biomol. Chem., 2016,14, 5832-5842\nThe effectiveness of computational tools in determining relative configurations of complex molecules is investigated, using natural products mandelalides A–D and coibamide A, towards a generalized recipe for the scientific community at large.\nC2-Alkenylation of N-heteroaromatic compounds via Brønsted acid catalysis\nGiacomo E. M. Crisenza, Elizabeth M. Dauncey and John F. Bower\nC2-alkenylated heteroaromatics can be accessed by simple Brønsted acid catalysed union of diverse heteroarene N-oxides with alkenes. The scope and limitations of the process are outlined.\nOrg. Biomol. Chem., 2016,14, 5820-5825\nThe effect of photoisomerization on the enzymatic hydrolysis of polymeric micelles bearing photo-responsive azobenzene groups at their cores\nAssaf J. Harnoy, Gadi Slor, Einat Tirosh and Roey J. Amir\nPhotoisomerization boosts the enzymatic disassembly of smart polymeric micelles based on amphiphilic PEG–dendron hybrids bearing enzymatically cleavable azobenzene end-groups.\nOrg. Biomol. Chem., 2016,14, 5813-5819\nSide-chain-to-tail cyclization of ribosomally derived peptides promoted by aryl and alkyl amino-functionalized unnatural amino acids\nJohn R. Frost, Zhijie Wu, Yick Chong Lam, Andrew E. Owens and Rudi Fasan\nA strategy for the production of side-chain-to-tail cyclic peptides from ribosomally derived polypeptide precursors is reported.\nOrg. Biomol. Chem., 2016,14, 5803-5812\nAsymmetric nucleophilic dearomatization of diazarenes by anion-binding catalysis\nTheresa Fischer, Julia Bamberger and Olga García Mancheño\nThe first highly regio- and enantioselective nucleophilic dearomatization of diazarenes by anion-binding organocatalysis is reported.\nOrg. Biomol. Chem., 2016,14, 5794-5802\nP. Bauer, Å. Janfalk Carlsson, B. A. Amrein, D. Dobritzsch, M. Widersten and S. C. L. Kamerlin\nComputational studies highlight the importance of conformational diversity in the enantioconvergent hydrolysis of styrene oxide by potato epoxide hydrolase 1.\nOrg. Biomol. Chem., 2016,14, 5639-5651\nNaatasha Isahak, Julie Sanchez, Sébastien Perrier, Martin J. Stone and Richard J. Payne\nThis paper describes the synthesis of polymers and silica nanoparticles, both bearing polystyrene sulfonate brushes, and the measurement of their binding affinity for the chemokine monocyte chemoattractant protein-1 (MCP-1) in monomeric and dimeric form.\nOrg. Biomol. Chem., 2016,14, 5652-5658\nVersatile, mild, and selective reduction of various carbonyl groups using an electron-deficient boron catalyst\nKatherine M. Lucas, Adam F. Kleman, Luke R. Sadergaski, Caitlyn L. Jolly, Brady S. Bollinger, Brittany L. Mackesey and Nicholas A. McGrath\nAcetanilides and nitriles are mildly and selectively reduced over various other carbonyl derivatives using an electron-deficient boron catalyst and triethylsilane.\nOrg. Biomol. Chem., 2016,14, 5774-5778\nThermodynamic origin of α-helix stabilization by side-chain cross-links in a small protein\nConor M. Haney, Halina M. Werner, James J. McKay and W. Seth Horne\nSide-chain cyclization has a consistent effect on protein folding energetics, and the identity of the cross-linking moiety determines the magnitude of stabilization.\nOrg. Biomol. Chem., 2016,14, 5768-5773\nBenzothiazole hydrazones of furylbenzamides preferentially stabilize c-MYC and c-KIT1 promoter G-quadruplex DNAs\nSushree Prangya Priyadarshinee Pany, Praneeth Bommisetti, K. V. Diveshkumar and P. I. Pradeepkumar\nThe stabilization of G-quadruplex DNA structures by using small molecule ligands having simple structural scaffolds has the potential to be harnessed for developing next generation anticancer agents.\nOrg. Biomol. Chem., 2016,14, 5779-5793\nSelective recognition of c-MYC G-quadruplex DNA using prolinamide derivatives\nAjay Chauhan, Sushovan Paladhi, Manish Debnath and Jyotirmayee Dash\nHerein we report the design, synthesis, biophysical and biological evaluation of triazole containing prolinamide derivatives as selective c-MYC G-quadruplex binding ligands.\nOrg. Biomol. Chem., 2016,14, 5761-5767\nAyumi Tsutsui, Akihiro Ogura, Tsuyoshi Tahara, Satoshi Nozaki, Sayaka Urano, Mitsuko Hara, Soichi Kojima, Almira Kurbangalieva, Hirotaka Onoe, Yasuyoshi Watanabe, Naoyuki Taniguchi and Katsunori Tanaka\nMolecular imaging visualized significantly reduced clearance of AGE-albumin.\nOrg. Biomol. Chem., 2016,14, 5755-5760\nLight-triggered assembly–disassembly of an ordered donor–acceptor π-stack using a photoresponsive dimethyldihydropyrene π-switch\nV. Siva Rama Krishna, Mousumi Samanta, Suman Pal, N. P. Anurag and Subhajit Bandyopadhyay\nA dimethyldihydropyrene based photochromic π-switch in its closed state forms donor–acceptor stacks with 1,4,5,8-naphthalenetetracarboxylic dianhydride. The stacks collapse in the photoisomeric open form.\nOrg. Biomol. Chem., 2016,14, 5744-5750\nSynthetic studies towards putative yuremamine using an iterative C(sp3)–H arylation strategy\nMatthew B. Calvert and Jonathan Sperry\nAn overview of synthetic efforts toward the initially proposed structure of yuremamine using iterative C(sp3)–H arylations is described.\nOrg. Biomol. Chem., 2016,14, 5728-5743\nA unified strategy for the palladium-catalyzed Suzuki–Miyaura cross-coupling of amides with boronic acids for the synthesis of ketones by N–C bond activation is reported.\nOrg. Biomol. Chem., 2016,14, 5690-5707\nReversible morphological changes of assembled supramolecular amphiphiles triggered by pH-modulated host–guest interactions\nM. A. Olson, M. S. Messina, J. R. Thompson, T. J. Dawson, A. N. Goldner, D. K. Gaspar, M. Vazquez, J. A. Lehrman and A. C.-H. Sue\nAcid–base modulated host–guest binding at the micellar–water interface triggers reversible oblate ellipsoid-to-lamellar morphological transitions revealing the relationship between and morphology.\nOrg. Biomol. Chem., 2016,14, 5714-5720\nGreen organocatalytic α-hydroxylation of ketones\nErrika Voutyritsa, Alexis Theodorou and Christoforos G. Kokotos\nAn efficient and green method for the α-hydroxylation of substituted ketones has been developed.\nOrg. Biomol. Chem., 2016,14, 5708-5713\nJ. M. Van Raden, E. R. Darzi, L. N. Zakharov and R. Jasti\nA highly-strained, nitrogen-doped cycloparaphenylene (CPP), azaCPP, was synthesized and then converted to a donor–acceptor nanohoop, N-methylazaCPP, via alkylation of the nitrogen center.\nOrg. Biomol. Chem., 2016,14, 5721-5727\nI2 mediated synthesis of 5-substituted-3-methyl/benzyl-1,3,4-oxadiazol-2(3H)-ones via sequential condensation/oxidative cyclization and rearrangement\nShyam Sunder Patel, Nisha Chandna, Shreemoyee Kumar and Nidhi Jain\nA simple and efficient iodine-assisted protocol for synthesis of 5-substituted-3-methyl/benzyl-1,3,4-oxadiazol-2(3H)-ones has been developed.\nOrg. Biomol. Chem., 2016,14, 5683-5689\nDirect conjugate alkylation of α,β-unsaturated carbonyls by TiIII-catalysed reductive umpolung of simple activated alkenes\nPlamen Bichovski, Thomas M. Haas, Manfred Keller and Jan Streuff\nThe title reaction leads to 1,6-difunctionalized products without the requirement of premetallated reagents. Details on scope, selectivity and mechanism are reported.\nOrg. Biomol. Chem., 2016,14, 5673-5682\nPaseka T. Moshapo, Mokela Sokamisa, Edwin M. Mmutlane, Richard M. Mampa and Henok H. Kinfe\nLewis acid-mediated three component coupling of salicyladehydes, anilines and gylcals provided novel benzopyran-fused pyranoquinolines stereoselectively, in moderate to high yields.\nOrg. Biomol. Chem., 2016,14, 5627-5638\nHsin Y. Su, Yixiong Song and Mark S. Taylor\nA protocol for the synthesis of chiral β-aminophosphines by ring-opening of cyclic sulfamidates with metallated secondary phosphine oxides is described. It allows access to previously unknown derivatives having electron-deficient, electron-rich and sterically hindered P-aryl substituents.\nOrg. Biomol. Chem., 2016,14, 5665-5672\nCatalytic asymmetric formal γ-allylation of deconjugated butenolides\nAmit K. Simlandy and Santanu Mukherjee\nOrg. Biomol. Chem., 2016,14, 5659-5664


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Kretzmann, Paul E. Ph. D., D. D. "Commentary on Ephesians:4 Overview". "Kretzmann's Popular Commentary". http://odl.studylight.org/commentaries/kpc/ephesians-0.html. 1921-23.


Khan, Shah Rukh7\nYash Raj Films7\nYash Raj Films Home Entertainment (Firm)6\nMotion pictures, Indic.32\nYou searched for: Subject Heading Browse Suites (Piano) Remove constraint Subject Heading Browse: Suites (Piano) Format Video Remove constraint Format: Video Form/Genre Romance films. Remove constraint Form/Genre: Romance films. Library Van Pelt-Dietrich Library Center Remove constraint Library: Van Pelt-Dietrich Library Center Record Source Penn Remove constraint Record Source: Penn Subject Motion pictures, Indic Remove constraint Subject: Motion pictures, Indic\nTaj Mahal (Agra, India)--Drama (1 record)


Altes Holz mit lilafarbenem Herz by Jeanette Dietl, Royalty free stock photos #35115686 on Fotolia.com\nAltes Holz mit lilafarbenem HerzJeanette Dietl09-04-2011Fotolia\n#35115686 - Altes Holz mit lilafarbenem Herz© Jeanette Dietl - See portfolio\nKeywords ["background","baptism","birth","birthday","blue","card","congratulation","contact","country style","craft","creative","dam","engagement","fast","fortune","greeting card","heart","hobby","homemade","invitation","magenta","mother's day","partnership","party","purple","rendez-vous","romance","romantic","rustic","style","symbol","textile","valentine","wedding","wedding dress","white","wish","wood grain"]\nbackground baptism birth birthday blue card congratulation contact country style craft creative dam engagement fast fortune greeting card heart hobby homemade invitation magenta mother's day partnership party purple rendez-vous romance romantic rustic style symbol textile valentine wedding wedding dress white wish wood grain\nThe photo "Altes Holz mit lilafarbenem Herz" from Jeanette Dietl is available on Fotolia under a Royalty Free license from 2 credits (Credit from $0.74).\nThe author of this picture, Jeanette Dietl also has 621 images in the same series.\nGlückspilz - Fliegenpilz mit Kleeblatt als GlückssymbolJeanette Dietl12-10-2013Fotolia\nKerze zum Geburtstag - Geburtstagskarte mit Text in BlauJeanette Dietl12-03-2013Fotolia\nWorte - Glückwunschkarte mit Kerzen blau und Liebe, GlückJeanette Dietl12-03-2013Fotolia


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Peter Pan: Return To Neverland Cheats, Cheat Codes, Hints and Video Walkthroughs for GameBoy Advance\nThu, 06 Dec 2007 00:00:00 Cheats, Hints & Walkthroughs\nPeter Pan: Return To Neverland Cheats for GameBoy Advance\nThis page contains Cheats for Peter Pan: Return To Neverland organized by sections for GameBoy Advance. This game has "Action Platformer" as genre, made by Crawfish Interactive, released on Feb 22, 2002. If you can't find a hint or secret in our list, then please check this page periodically for the latest updates.\nCartoon Network Block Party, (GBA)


"It was a great opportunity to work with Tesco's designers for the concept store in Llansamlet, Swansea in Wales. In the first project planning phase, Wanzl's design and development team devised a creative concept and brought it to fruition over many months in close cooperation with Tesco.\nTesco's brief was to create a customer-friendly shop environment that highlights brand value, linked with excellent customer communication. The order was to refresh and reposition the shopping experience as the existing in-store promotions were interrupting the walkways through the store. For the market re-launch, we installed our wire tech shop fitout system in the food area – for Wanzl, this was a first at Tesco. Our new temperature-controlled sales module, YourTable Cool, presents fresh and healthy ready-to-go goods for convenience products and cross-selling. The new shop layout is consistently continued in-store: in the service area, in the F&F textile shop with presentation systems that are more than four meters high and have six integrated digital screens, in the serving area with fresh delicatessen, meat, sausage and fish as well as in the alcoholic beverages section. Customised systems in the food section, special bakery and wine tables and six promotional units support the high-revenue secondary placement of campaign and seasonal offers."


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News > The Voice\nThe Voice Calls In Back Up\n08 May 2012 The Voice and Britain’s got Talent (BGT) have been at war, and now things are hotting up with the inclusion of super stars Kylie Minogue and Cheryl Cole being drafted in as part of the semi-finals (26th May 2012) and finals 2nd June 2012.\nJudges on The Voice have been criticised for not being ‘mean enough’ to the contestants and have been asked to get tougher in a bid to compete with BGT!A source said of The Voice: “It’s the first year of the show and clearly it needs some tweaking.”Losing more than 2 million viewers from BGT, The Voice Live Tour has a lot of high expectations to live up to, when seven of the contestants and the winner travel the UK and perform on their arena tour!You can now secure The Voice tickets on Ticketmaster’s GET ME IN! ticket market.