Amino−Zinc−Enolate Carbometalation Reactions: Application to Ring Closure of Terminally Substituted Olefin for the Asymmetric Synthesis of cis- and trans-3-Prolinoleucine-Reference-Cited by-同舟云学术

Amino−Zinc−Enolate Carbometalation Reactions: Application to Ring Closure of Terminally Substituted Olefin for the Asymmetric Synthesis of cis- and trans-3-Prolinoleucine

Published:2003-02-13 Issue:6 Volume:68 Page:2256-2265
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Karoyan Philippe¹,Quancard Jean¹,Vaissermann Jacqueline¹,Chassaing Gérard¹

Affiliation:

1. UMR CNRS 7613, Structure et Fonction de Molécules Bioactives, Université Paris VI, case 45, 4 place Jussieu 75252 Paris Cedex 05, France, and URA CNRS 400, Chimie des Métaux de Transition, Université Paris VI, case 42, 4 place Jussieu 75252 Paris cedex 05, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo026535n

Reference78 articles.

1. Anionic cyclization of olefinic alkyllithiums: ring closure of terminally substituted 5-hexenyllithiums.

2. Intramolecular Metallo-Ene-Allene Reactions. A New Carbocycles Synthesis

3. Carbocyclization Reaction of Active Methine Compounds with Unactivated Alkenyl or Alkynyl Groups Mediated by TiCl4−Et3N

4. New strategy for the synthesis of 3-substituted prolines

5. Zinca-ene-allene and zinc-enolate cyclization. Towards the synthesis of polysubstituted pyrrolidines

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