Transmetalation reactions in organocopper chemistry

Wipf, P (1993) Transmetalation reactions in organocopper chemistry. Synthesis (6). 537 - 557. ISSN 0039-7881

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Abstract

The preparation of organocopper reagents by transmetalation protocols has emerged as a versatile new tool for selective C,C-bond formation. In this review, the use of organoaluminum, -boron, -lead, -manganese, -mercury, -samarium, -stannane, -telluride, -titanium, -zinc, and -zirconocene derivatives for the preparation of copper complexes is presented and compared to traditional protocols originating from lithium or magnesium organometallics. Significantly, a wide range of functionality is generally tolerated in the transmetalation procedures, and the reactivity of the resulting cuprates depends on the presence of the residual metal salts. The use of these heterobimetallic cuprates in natural product synthesis demonstrates some of the key features of this new methodology.

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Details

Item Type:	Article
Status:	Published
Creators/Authors:	Creators Email Pitt Username ORCID Wipf, P pwipf@pitt.edu PWIPF
Date:	1 January 1993
Date Type:	Publication
Journal or Publication Title:	Synthesis
Number:	6
Page Range:	537 - 557
DOI or Unique Handle:	10.1055/s-1993-25900
Schools and Programs:	Dietrich School of Arts and Sciences > Chemistry
Refereed:	Yes
ISSN:	0039-7881
Article Type:	Review
Date Deposited:	06 Oct 2015 14:55
Last Modified:	02 Aug 2020 13:57
URI:	http://d-scholarship.pitt.edu/id/eprint/25725

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