Stereocontrolled Synthesis of Highly Substituted Proline Esters via [3 + 2] Cycloaddition between N-Metalated Azomethine Ylides and Nitroalkenes. Origins of the Metal Effect on the Stereochemical Outcome-Reference-Cited by-同舟云学术

Stereocontrolled Synthesis of Highly Substituted Proline Esters via [3 + 2] Cycloaddition between N-Metalated Azomethine Ylides and Nitroalkenes. Origins of the Metal Effect on the Stereochemical Outcome

Published:1998-02-24 Issue:6 Volume:63 Page:1795-1805
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ayerbe Mirari¹,Arrieta Ana¹,Cossío Fernando P.¹,Linden Anthony²

Affiliation:

1. Kimika Fakultatea, Euskal Herriko Unibertsitatea, P.K. 1072, San Sebastián-Donostia, Spain

2. Organisch-chemisches Insitut der Universität Zurich,Winterthurestrasse 190, CH-8057, Zurich, Switzerland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo971212q

Reference66 articles.

1. (a) Pichon, M.; Figadère, B.Tetrahedron: Asymmetry1996,7, 927.

2. Regioselective Enolization and Alkylation of 4-Oxo-N-(9-phenylfluoren-9-yl)proline: Synthesis of Enantiopure Proline−Valine and Hydroxyproline−Valine Chimeras

3. Stereoselective Addition of Grignard-Derived Organocopper Reagents to N-Acyliminium Ions: Synthesis of Enantiopure 5- and 4,5-Substituted Prolinates

4. Synthesis of Enantiopure 1,2-Didehydropyrrolidine, D-Proline, and Oxazoline Derivatives via Staudinger-Aza-Wittig Cyclization of γ-Azido Aldehydes

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