Nucleophilic ring opening of epoxides by carbanions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference34 articles.
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1. A new synthetic approach to 2,3-dideoxy-2-fluoro-β-d-threo-pentofuranose, the fluorofuranose unit of the anti-HIV-active nucleoside, β-FddA;Tetrahedron Letters;2004-01
2. Synthesis of New Heterocycles through a Cation-Driven Tandem Ring-Enlargement−Annulation Reaction;Organic Letters;2002-06-27
3. Trapping of 1,2-benzo-1,3,4-cycloheptatriene as evidence for a strained cyclic allene structure;Tetrahedron;1999-07
4. An interesting ring contraction of a class of bromohydrins and trans-dibromides;Tetrahedron Letters;1984-01
5. ChemInform Abstract: NUCLEOPHILIC RING OPENING OF EPOXIDES BY CARBANIONS. NOVEL FORMATION OF CYCLOPROPANE DERIVATIVES IN A NONPOLAR SOLVENT;Chemischer Informationsdienst;1983-12-20
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