Stereoelectronic control of the rate of ring opening in azidofurans
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Reactions in the conjugated ‘ene–ene–yne’ manifold: five-membered ring fragmentation and ring formation via coarctate/pseudocoarctate mechanisms;Chem. Soc. Rev.;2008
2. New insight into experimental and theoretical properties of some para-like substituted 2-azidothiophenes;Journal of the Chemical Society, Perkin Transactions 2;1999
3. One-pot preparation of isomeric acetyl- and 2,2,2-trifluoroacetyl-azidothiophenes by selective bifunctionalization of dibromothiophenes via halogen–lithio exchange;J. Chem. Soc., Perkin Trans. 1;1996
4. Synthesis and thermal reactivity of 2-azido-5-trimethylsilylthiophene and 2-azido-5-methylthiophene. The para-like substituent effect on fragmentation of the azido group;Journal of the Chemical Society, Perkin Transactions 1;1995
5. Organizing Principle of Complex Reactions and Theory of Coarctate Transition States;Angewandte Chemie International Edition in English;1994-02-18
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