Chemistry of Sulfonate‐ and Sulfonamide‐Stabilized Carbanions − The CSIC Reactions-Reference-Cited by-同舟云学术

Chemistry of Sulfonate‐ and Sulfonamide‐Stabilized Carbanions − The CSIC Reactions

Published:2003-09-16 Issue:19 Volume:2003 Page:3713-3726
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Postel Denis¹,Van Nhien Albert Nguyen¹,Marco José L.²

Affiliation:

1. Laboratoire des Glucides, Faculté des Sciences − UPJV, 33 rue St Leu, 80039 Amiens Cedex, France, Fax: (internat.) + 33‐3/22827568

2. Laboratorio de Radicales Libres (LRL), IQOG(CSIC), Juan de la Cierva, 3; 28006 Madrid, Spain, Fax: (internat.) + 34‐91/564‐4853

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.200300170

Reference147 articles.

1. D. J. Cram Fundamentals of Carbanion Chemistry Academic Press New York 1965 pp. 48−52.

3. G. Solladié M. C. Carreño “Optically Active β‐Keto Sulfoxides and Analogues in Asymmetric Synthesis” inOrganosulfur Chemistry Synthetic Aspects(Ed.: P. Page) Academic Press London 1995 pp. 1−47.

4. Asymmetric Synthesis Using Nucleophilic Reagents Containing a Chiral Sulfoxide Group

5. We agree with the criticism of one of the referees regarding the use of new name reactions for very well known processes in synthetic organic chemistry but in this case we think that the use of theCSICterm is largely justified in view of number and importance of cases in whichCarbanion‐mediatedSulfur (Sulfonates Sulfonamides Sulfoxides orSulfones) containing molecules have been applied for the formation of carbon−carbon bonds in inter‐ or intramolecular processes.

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