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1,2,3-Triazoles as peptide bond isosteres: synthesis and biological evaluation of cyclotetrapeptide mimics

Bock, Victoria D.; Speijer, Dave; Hiemstra, Henk; van Maarseveen, Jan H.; Bock Victoria D.; Van't Hoff Institute for Molecular Sciences, University of Amsterdam; Speijer Dave; Department of Medical Biochemistry, Academic Medical Center, University of Amsterdam; Hiemstra Henk; Van't Hoff Institute for Molecular Sciences, University of Amsterdam; van Maarseveen Jan H.; Van't Hoff Institute for Molecular Sciences, University of Amsterdam (Royal Society of Chemistry, 2007)
1,2-Chlorine atom migration in 3-chloro-2-butyl radicals: a computational studyElectronic supplementary information (ESI) available: Calculated energies and enthalpies of stationary points, full structural information, and structures of trans-but-2-ene (9) and trans-but-2-ene radical (10). See http://www.rsc.org/suppdata/ob/b2/b209981k/

Neumann, Bernd; Zipse, Hendrik; Neumann Bernd; Department Chemie, Ludwig-Maximilians-UniversitÃ¤t MÃ¼nchen; Zipse Hendrik; Department Chemie, Ludwig-Maximilians-UniversitÃ¤t MÃ¼nchen (Royal Society of Chemistry, 2002)
1,3,5-Tristyrylbenzene dendrimers: a novel model system to explore oxygen quenching in a highly organized environment

Uda, Mayuko; Momotake, Atsuya; Arai, Tatsuo; Uda Mayuko; Department of Chemistry, University of Tsukuba; Momotake Atsuya; Department of Chemistry, University of Tsukuba; Arai Tatsuo; Department of Chemistry, University of Tsukuba (Royal Society of Chemistry, 2003)
1,3-Alternate calix[4]arenes, selectively functionalized by amino groups

Danila, Crenguta; Bolte, Michael; Böhmer, Volker; Danila Crenguta; Fachbereich Chemie und Pharmazie, Abteilung Lehramt Chemie, Johannes Gutenberg-UniversitÃ¤t; Bolte Michael; Institut fÃ¼r Organische Chemie, Johann Wolfgang von Goethe UniversitÃ¤t; BÃ¶hmer Volker; Fachbereich Chemie und Pharmazie, Abteilung Lehramt Chemie, Johannes Gutenberg-UniversitÃ¤t (Royal Society of Chemistry, 2005)
1,3-Bis(diarylmethylidene)-2-methylidenecyclohexanes in cycloaddition and cyclodimerization reactions. The role of stereoelectronic factors

Klimova, Elena I.; García, Marcos Martínez; Klimova, Tatiana; Ortega, S. Hernandez; Bakinovsky, Leon V.; Klimova Elena I.; Universidad Nacional AutÃ³noma de MÃ©xico, Facultad de QuÃmica, Cd. Universitaria, CoyoacÃ¡n; GarcÃa Marcos MartÃnez; Universidad Nacional AutÃ³noma de MÃ©xico, Instituto de QuÃmica, Cd. Universitaria, CoyoacÃ¡n; Klimova Tatiana; Universidad Nacional AutÃ³noma de MÃ©xico, Facultad de QuÃmica, Cd. Universitaria, CoyoacÃ¡n; Ortega S. Hernandez; Universidad Nacional AutÃ³noma de MÃ©xico, Instituto de QuÃmica, Cd. Universitaria, CoyoacÃ¡n; Bakinovsky Leon V.; N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences (Royal Society of Chemistry, 2003)
1,3-Dipolar character of 2-vinyl quinazoline 3-oxides; first and second generation cycloaddition products

Heaney, Frances; Lawless, Elaine; Mahon, Mary; McArdle, Patrick; Cunningham, Desmond; Heaney Frances; Department of Chemistry, National University of Ireland; Lawless Elaine; Department of Chemistry, National University of Ireland; Mahon Mary; Department of Chemistry, University of Bath; McArdle Patrick; Department of Chemistry, National University of Ireland; Cunningham Desmond; Department of Chemistry, National University of Ireland (Royal Society of Chemistry, 2006)
1,5-Asymmetric induction of chirality using π-allyltricarbonyliron lactone complexes: highly diastereoselective synthesis of α-functionalised carbonyl compounds

Hollowood, Christopher J.; Ley, Steven V.; Wright, Edward A.; Hollowood Christopher J.; Department of Chemistry, University of Cambridge; Ley Steven V.; Department of Chemistry, University of Cambridge; Wright Edward A.; Department of Chemistry, University of Cambridge (Royal Society of Chemistry, 2003)
1,N6-Etheno-7-deaza-2,8-diazaadenosine: syntheses, properties and conversion to 7-deaza-2,8-diazaadenosine

Lin, Wenqing; Li, Hong; Ming, Xin; Seela, Frank; Lin Wenqing; Laboratorium fÃ¼r Organische und Bioorganische Chemie, Institut fÃ¼r Chemie, UniversitÃ¤t OsnabrÃ¼ck; Center for Nanotechnology (CeNTech); Li Hong; Laboratorium fÃ¼r Organische und Bioorganische Chemie, Institut fÃ¼r Chemie, UniversitÃ¤t OsnabrÃ¼ck; Center for Nanotechnology (CeNTech); Ming Xin; Laboratorium fÃ¼r Organische und Bioorganische Chemie, Institut fÃ¼r Chemie, UniversitÃ¤t OsnabrÃ¼ck; Center for Nanotechnology (CeNTech); Seela Frank; Laboratorium fÃ¼r Organische und Bioorganische Chemie, Institut fÃ¼r Chemie, UniversitÃ¤t OsnabrÃ¼ck; Center for Nanotechnology (CeNTech) (Royal Society of Chemistry, 2005)
1-Ethynylpyrene-modified guanine and cytosine as optical labels for DNA hybridization

Wagner, Clemens; Rist, Manuela; Mayer-Enthart, Elke; Wagenknecht, Hans-Achim; Wagner Clemens; Technical University of Munich, Chemistry Department; Rist Manuela; Technical University of Munich, Chemistry Department; Mayer-Enthart Elke; Technical University of Munich, Chemistry Department; Wagenknecht Hans-Achim; Technical University of Munich, Chemistry Department (Royal Society of Chemistry, 2005)
1-Oxabicyclic β-lactams as new inhibitors of elongating MPT–a key enzyme responsible for assembly of cell-surface phosphoglycans of Leishmania parasite

Ruhela, Dipali; Chatterjee, Patrali; Vishwakarma, Ram A.; Ruhela Dipali; Bio-organic Chemistry Lab, National Institute of Immunology; Chatterjee Patrali; Bio-organic Chemistry Lab, National Institute of Immunology; Vishwakarma Ram A.; Bio-organic Chemistry Lab, National Institute of Immunology (Royal Society of Chemistry, 2005)
15N CIDNP investigations of the peroxynitric acid nitration of l-tyrosine and of related compounds

Lehnig, Manfred; Kirsch, Michael; Lehnig Manfred; Organische Chemie, UniversitÃ¤t Dortmund; Kirsch Michael; Institut fÃ¼r Physiologische Chemie, UniversitÃ¤tsklinikum Essen (Royal Society of Chemistry, 2006)
15NH4+ion movement inside d(G4T4G4)2G-quadruplex is accelerated in the presence of smaller Na+ions

Šket, Primož; Črnugelj, Martin; Koźmiński, Wiktor; Plavec, Janez; Å ket PrimoÅ¾; NMR center, National Institute of Chemistry; Ä rnugelj Martin; NMR center, National Institute of Chemistry; KoÅºmiÅ ski Wiktor; Department of Chemistry, University of Warsaw; Plavec Janez; NMR center, National Institute of Chemistry (Royal Society of Chemistry, 2004)
1H and13C NMR characterization of pyridinium-type isoniazid–NAD adducts as possible inhibitors of InhA reductase of Mycobacterium tuberculosis

Broussy, Sylvain; Bernardes-Génisson, Vania; Coppel, Yannick; Quémard, Annaïk; Bernadou, Jean; Meunier, Bernard; Broussy Sylvain; Laboratoire de Chimie de Coordination du CNRS; Bernardes-GÃ©nisson Vania; Laboratoire de Chimie de Coordination du CNRS; Coppel Yannick; Laboratoire de Chimie de Coordination du CNRS; QuÃ©mard AnnaÃ¯k; Institut de Pharmacologie et de Biologie Structurale du CNRS; Bernadou Jean; Laboratoire de Chimie de Coordination du CNRS; Meunier Bernard; Laboratoire de Chimie de Coordination du CNRS (Royal Society of Chemistry, 2005)
1H-1,3-Diazepines, 5H-1,3-diazepines, 1,3-diazepinones, and 2,4-diazabicyclo[3.2.0]heptenes,

Reisinger, Ales; Koch, Rainer; Bernhardt, Paul V.; Wentrup, Curt; Reisinger Ales; Department of Chemistry, School of Molecular and Microbial Sciences, The University of Queensland; Koch Rainer; Institut fÃ¼rReine und Angewandte Chemie, Carl von Ossietetzky UniversitÃ¤t; Bernhardt Paul V.; Department of Chemistry, School of Molecular and Microbial Sciences, The University of Queensland; Wentrup Curt; Department of Chemistry, School of Molecular and Microbial Sciences, The University of Queensland (Royal Society of Chemistry, 2004)
(1R,4S,5R)-3-Fluoro-1,4,5-trihydroxy-2-cyclohexene-1-carboxylic acid: the fluoro analogue of the enolate intermediate in the reaction catalyzed by type II dehydroquinases

Frederickson, Martyn; Roszak, Aleksander W.; Coggins, John R.; Lapthorn, Adrian J.; Abell, Chris; Frederickson Martyn; University Chemical Laboratory; Roszak Aleksander W.; Department of Chemistry, University of Glasgow; Coggins John R.; Division of Biochemistry and Molecular Biology, Institute of Biomedical and Life Sciences, University of Glasgow; Lapthorn Adrian J.; Department of Chemistry, University of Glasgow; Abell Chris; University Chemical Laboratory (Royal Society of Chemistry, 2004)
2,3-Disubstituted indoles from olefins and hydrazinesvia tandem hydroformylation–Fischer indole synthesis and skeletal rearrangement

Linnepe (née Köhling), Petra; Schmidt, Axel M.; Eilbracht, Peter; Linnepe (nÃ©e KÃ¶hling) Petra; Fachbereich Chemie, Organische Chemie I, UniversitÃ¤t Dortmund; Schmidt Axel M.; Fachbereich Chemie, Organische Chemie I, UniversitÃ¤t Dortmund; Eilbracht Peter; Fachbereich Chemie, Organische Chemie I, UniversitÃ¤t Dortmund (Royal Society of Chemistry, 2006)
2,4-Dithiouracil: the reproducible H-bonded structural motifs in the complexes with 18-membered crown ethers

Wang, Wen-Jwu; Ganin, Eduard V.; Fonari, Marina S.; Simonov, Yurii A.; Bocelli, Gabriele; Wang Wen-Jwu; Department of Chemistry Tamkang University; Ganin Eduard V.; Department of Chemistry Tamkang University; Fonari Marina S.; Institute of Applied Physics Academy of Sciences of Moldova Academy; Simonov Yurii A.; Institute of Applied Physics Academy of Sciences of Moldova Academy; Bocelli Gabriele; IMEM-CNR (Royal Society of Chemistry, 2005)
2,5-Disubstituted pyrrolidines: synthesis by enamine reduction and subsequent regioselective and diastereoselective alkylations

Hussaini, Syed Raziullah; Moloney, Mark G.; Hussaini Syed Raziullah; The Department of Chemistry, Chemistry Research Laboratory, The University of Oxford; Moloney Mark G.; The Department of Chemistry, Chemistry Research Laboratory, The University of Oxford (Royal Society of Chemistry, 2006)
2,5-Disubstituted pyrrolidines: versatile regioselective and diastereoselective synthesis by enamine reduction and subsequent alkylation

Hussaini, Syed Raziullah; Moloney, Mark G.; Hussaini Syed Raziullah; The Department of Chemistry, Dyson Perrins Laboratory, The University of Oxford; Moloney Mark G.; The Department of Chemistry, Dyson Perrins Laboratory, The University of Oxford (Royal Society of Chemistry, 2003)
2-(4-Tolylsulfonyl)ethoxymethyl (TEM)—a new 2′-OH protecting group for solid-supported RNA synthesis

Zhou, Chuanzheng; Honcharenko, Dmytro; Chattopadhyaya, Jyoti; Zhou Chuanzheng; Department of Bioorganic Chemistry, Box 581, Biomedical Center, Uppsala University; Honcharenko Dmytro; Department of Bioorganic Chemistry, Box 581, Biomedical Center, Uppsala University; Chattopadhyaya Jyoti; Department of Bioorganic Chemistry, Box 581, Biomedical Center, Uppsala University (Royal Society of Chemistry, 2007)

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