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Contents list for Organic & Biomolecular Chemistry, issue 21, 2003
Front Cover
Comment
The Dyson Perrins Laboratory at Oxford
Org. Biomol. Chem., 2003, 1, 3625
DOI: 10.1039/b309390p
Communications
Synthesis and properties of hetero-halogenated TTFs
Rie Suizu and Tatsuro Imakubo,
Org. Biomol. Chem., 2003, 1, 3629
DOI: 10.1039/b310822h
Enhanced 13C resolution in semi-selective HMBC: a band-selective, constant-time HMBC for complex organic structure elucidation by NMR
Tim D. W. Claridge and Ignacio Pérez-Victoria,
Org. Biomol. Chem., 2003, 1, 3632
DOI: 10.1039/b307122g
Stereospecificity in the silicon tethered 
-(methyl)allylation of aldehydes
Jeremy Robertson, Michael J. Hall and Stuart P. Green,
Org. Biomol. Chem., 2003, 1, 3635
DOI: 10.1039/b306920f
Synthesis and crystal structure of a meso-trialkynyl-[28]hexaphyrin
Alexander Krivokapic and Harry L. Anderson,
Org. Biomol. Chem., 2003, 1, 3639
DOI: 10.1039/b306725b
Glycosyl phenylthiosulfonates (Glyco-PTS): novel reagents for glycoprotein synthesis
David P. Gamblin, Philippe Garnier, Sarah J. Ward, Neil J. Oldham, Antony J. Fairbanks and Benjamin G. Davis,
Org. Biomol. Chem., 2003, 1, 3642
DOI: 10.1039/b306990g
Non-denaturing electrospray ionisation-mass spectrometry reveals ligand selectivity in histamine-binding protein RaHBP2
Neil J. Oldham, Olga Lissina, Miles A. Nunn and Guido C. Paesen,
Org. Biomol. Chem., 2003, 1, 3645
DOI: 10.1039/b306929j
Papers
Bend ribbon-forming tetrahydrofuran amino acids
Martin D. Smith, Timothy D. W. Claridge, Mark S. P. Sansom and George W. J. Fleet,
Org. Biomol. Chem., 2003, 1, 3647
DOI: 10.1039/b307707c
Synthesis of potent CXCR4 inhibitors possessing low cytotoxicity and improved biostability based on T140 derivatives
Hirokazu Tamamura, Kenichi Hiramatsu, Shuichi Kusano, Shigemi Terakubo, Naoki Yamamoto, John O. Trent, Zixuan Wang, Stephen C. Peiper, Hideki Nakashima, Akira Otaka and Nobutaka Fujii,
Org. Biomol. Chem., 2003, 1, 3656
DOI: 10.1039/b306473p
Enhancement of the T140-based pharmacophores leads to the development of more potent and bio-stable CXCR4 antagonists
Hirokazu Tamamura, Kenichi Hiramatsu, Makiko Mizumoto, Satoshi Ueda, Shuichi Kusano, Shigemi Terakubo, Miki Akamatsu, Naoki Yamamoto, John O. Trent, Zixuan Wang, Stephen C. Peiper, Hideki Nakashima, Akira Otaka and Nobutaka Fujii,
Org. Biomol. Chem., 2003, 1, 3663
DOI: 10.1039/b306613b
Biomimetic studies on polyenes
John E. Moses, Jack E. Baldwin, Sébastien Brückner, Serena J. Eade and Robert M. Adlington,
Org. Biomol. Chem., 2003, 1, 3670
DOI: 10.1039/b306933h
An approach to the generation of simple analogues of the antitumour agent spicamycin
Stéphane Mons and George W. J. Fleet,
Org. Biomol. Chem., 2003, 1, 3685
DOI: 10.1039/b307795k
A novel method for the synthesis of 4
-thiopyrimidine nucleosides using hypervalent iodine compounds
Naozumi Nishizono, Ryosuke Baba, Chika Nakamura, Kazuaki Oda and Minoru Machida,
Org. Biomol. Chem., 2003, 1, 3692
DOI: 10.1039/b305644a
Asymmetric synthesis of (1R,2S,3R)-3-methylcispentacin and (1S,2S,3R)-3-methyltranspentacin by kinetic resolution of tert-butyl (±)-3-methylcyclopentene-1-carboxylate
Mark E. Bunnage, Ann M. Chippindale, Stephen G. Davies, Richard M. Parkin, Andrew D. Smith and Jonathan M. Withey,
Org. Biomol. Chem., 2003, 1, 3698
DOI: 10.1039/b306935b
Asymmetric synthesis of anti-(2S,3S)- and syn-(2R,3S)-diaminobutanoic acid
Mark E. Bunnage, Anthony J. Burke, Stephen G. Davies, Nicholas L. Millican, Rebecca L. Nicholson, Paul M. Roberts and Andrew D. Smith,
Org. Biomol. Chem., 2003, 1, 3708
DOI: 10.1039/b306936m
Synthetic studies towards the tunicamycins and analogues based on diazo chemistry. Total synthesis of tunicaminyl uracil
Francisco Sarabia, Laura Martín-Ortiz and F. Jorge López-Herrera,
Org. Biomol. Chem., 2003, 1, 3716
DOI: 10.1039/b307674a
A multicomponent coupling strategy suitable for the synthesis of the triene component of the oxazolomycin antibiotics
Paul G. Bulger, Mark G. Moloney and Paul C. Trippier,
Org. Biomol. Chem., 2003, 1, 3726
DOI: 10.1039/b306925g
Synthesis of hydroxymethyl branched [3.2.0]bicyclic nucleosides using a regioselective oxetane ring-formation
Nanna K. Christensen, Ann Katrine L. Andersen, Trine R. Schultz and Poul Nielsen,
Org. Biomol. Chem., 2003, 1, 3738
DOI: 10.1039/b307667a
Scope of the reductive aldol reaction: application to aromatic carbocycles and heterocycles
Timothy J. Donohoe, David House and K. W. Ace,
Org. Biomol. Chem., 2003, 1, 3749
DOI: 10.1039/b306937k
Ene cyclisations of -(prenyl)dialkylsilyloxy aldehydes: formation and oxidative cleavage of oxasilacyclohexanols
Jeremy Robertson, Michael J. Hall, Petra M. Stafford and Stuart P. Green,
Org. Biomol. Chem., 2003, 1, 3758
DOI: 10.1039/b306922m
Nitrenium ions. Reactions of N,N-dimethyl-p-benzoyloxyaniline-iminium chloride with indoles and indolizines. X-ray structure of unexpected [2-chloro-4-(4-dimethylaminophenyl-ONN-azoxy)phenyl]dimethylamine (azoxy derivative)
Lucedio Greci, Riccardo Castagna, Patricia Carloni, Pierluigi Stipa, Corrado Rizzoli, Lara Righi and Paolo Sgarabotto,
Org. Biomol. Chem., 2003, 1, 3768
DOI: 10.1039/b308088a
Stereoselective synthesis of C-glycosides from carboxylic acids: the tandem Tebbe–Claisen approach
H. Yasmin Godage, David J. Chambers, Graham R. Evans and Antony J. Fairbanks,
Org. Biomol. Chem., 2003, 1, 3772
DOI: 10.1039/b306675b
Development of two processes for the synthesis of bridged azabicyclic systems: intermolecular radical addition–homoallylic rearrangements leading to 2-azanorborn-5-enes and neophyl-type radical rearrangements to 2-azabenzonorbornanes
David M. Hodgson, Magnus W. P. Bebbington and Paul Willis,
Org. Biomol. Chem., 2003, 1, 3787
DOI: 10.1039/b306717n
Control of diastereoselectivity in the crotylation and cinnamylation of aldehydes by the selection of ligands on allylic indium reagents
Tsunehisa Hirashita, Toshiya Kamei, Makoto Satake, Tomoaki Horie, Hidetaka Shimizu and Shuki Araki,
Org. Biomol. Chem., 2003, 1, 3799
DOI: 10.1039/b306195g
Synthesis of N-acyl-N,,-trialkyl and N-acyl-,-dialkyl glycines by selective cleavage of Ugi–Passerini adducts. Qualitative assessment of the effect of substituents on the path and yield of reaction
Wei-Qun Jiang, Susana P. G. Costa and Hernâni L. S. Maia,
Org. Biomol. Chem., 2003, 1, 3804
DOI: 10.1039/b307111c
Reflections on spontaneous asymmetric synthesis by amplifying autocatalysis
Ilya D. Gridnev, Joerg M. Serafimov, Harry Quiney and John M. Brown,
Org. Biomol. Chem., 2003, 1, 3811
DOI: 10.1039/b307382n
Synthesis of unprotected and borane-protected cyclic phosphines using Ru– and Mo– based olefin metathesis catalysts
Catherine A. Slinn, Alison J. Redgrave, S. Lucy Hind, Chris Edlin, Steven P. Nolan and Veronique Gouverneur,
Org. Biomol. Chem., 2003, 1, 3820
DOI: 10.1039/b306940k
Precise structure activity relationships in asymmetric catalysis using carbohydrate scaffolds to allow ready fine tuning: dialkylzinc–aldehyde additions
Daniel P. G. Emmerson, Renaud Villard, Claudia Mugnaini, Andrei Batsanov, Judith A. K. Howard, William P. Hems, Robert P. Tooze and Benjamin G. Davis,
Org. Biomol. Chem., 2003, 1, 3826
DOI: 10.1039/b309715n
Investigation of the configuration of alkyl phenyl ketone phenylhydrazones from ab initio1H NMR chemical shifts
Mahmoud Trabelsi, Mansour Salem and Benoît Champagne,
Org. Biomol. Chem., 2003, 1, 3839
DOI: 10.1039/b307528a
Formation of gold-like metal-lustrous inclusion crystals from 1-phenyl-2,5-bis[5-(tricyanoethenyl)-2-thienyl]pyrrole host and an electron-donating aromatic guest
Katsuyuki Ogura, Rui Zhao, Takashi Mizuoka, Motohiro Akazome and Shoji Matsumoto,
Org. Biomol. Chem., 2003, 1, 3845
DOI: 10.1039/b302689b
Hindered fluorescence quenching in an insulated molecular wire
Peter N. Taylor, Andrew J. Hagan and Harry L. Anderson,
Org. Biomol. Chem., 2003, 1, 3851
DOI: 10.1039/b306727k
Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at 
-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogens
Hidemitsu Uno, Kentarou Inoue, Takashi Inoue and Noboru Ono,
Org. Biomol. Chem., 2003, 1, 3857
DOI: 10.1039/b307132d
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