Artigo Revisado por pares

Arene Chromium Tricarbonyl Stabilised Benzylic Carbocations

1993; Thieme Medical Publishers (Germany); Volume: 1993; Issue: 05 Linguagem: Inglês

10.1055/s-1993-22443

ISSN

1437-2096

Autores

Stephen G. Davies, Timothy J. Donohoe,

Tópico(s)

Synthesis and Biological Activity

Resumo

The ability of the chromium tricarbonyl unit to stabilise benzylic carbocations and oxonium ions is described. We have investigated the use of arene chromium tricarbonyl complexes as chiral auxiliaries for asymmetric synthesis. The synthesis of homochiral tetrahydroisoquinolines, tetrahydrobenzazepines, and 2-aryltetrahydropyrans via intramolecular cyclisation of a nucleophile onto chromium tricarbonyl stabilised benzylic carbocations and oxonium ions is described. 1. Introduction 2. Evidence for the Chromium Tricarbonyl Stabilisation of Benzylic Carbocations 3. Acyclic Systems without ortho Substitution 3.1 Carbocations 3.2 Oxonium Ions 4. Bicyclic Complexes 4.1 (6-5) Ring Systems 4.2 (6-6) Ring Systems 5. ortho Substituted Acyclic Compounds 5.1 Carbocations 5.2 Oxonium Ions 6. Miscellaneous Applications of Chromium Tricarbonyl Stabilised Carbocations

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