Chemoselectivity of rhodium carbenoids. A comparison of the selectivity for OH insertion reactions or carbonyl ylide formation versus aliphatic and aromatic CH insertion and cyclopropanation-Reference-Cited by-同舟云学术

Chemoselectivity of rhodium carbenoids. A comparison of the selectivity for OH insertion reactions or carbonyl ylide formation versus aliphatic and aromatic CH insertion and cyclopropanation

Published:1993-06 Issue:23 Volume:49 Page:5109-5126
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Cox Geoffrey G.,Moody Christopher J.,Austin David J.,Padwa Albert

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference50 articles.

1. Catalytic methods for metal carbene transformations

2. Electrophilic metal carbenes as reaction intermediates in catalytic reactions

3. Transition-metal catalyzed decomposition of aliphatic diazo compounds — New results and applications in organic synthesis

4. Rhodium (II) catalyzed reactions of diazo-carbonyl compounds

5. Ylide formation from the reaction of carbenes and carbenoids with heteroatom lone pairs

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