A Thermodynamic Preference of Chiral N-Methanesulfonyl and N-Arenesulfonyl 2,3-cis-3-Alkyl-2-Vinylaziridines over Their 2,3-Trans-Isomers: Useful Palladium(0)-Catalyzed Equilibration Reactions for the Synthesis of (E)-Alkene Dipeptide Isosteres-Reference-Cited by-同舟云学术

A Thermodynamic Preference of Chiral N-Methanesulfonyl and N-Arenesulfonyl 2,3-cis-3-Alkyl-2-Vinylaziridines over Their 2,3-Trans-Isomers: Useful Palladium(0)-Catalyzed Equilibration Reactions for the Synthesis of (E)-Alkene Dipeptide Isosteres

Published:1997-02-01 Issue:4 Volume:62 Page:999-1015
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ibuka Toshiro¹,Mimura Norio¹,Aoyama Hiroshi¹,Akaji Masako¹,Ohno Hiroaki¹,Miwa Yoshihisa¹,Taga Tooru¹,Nakai Kazuo¹,Tamamura Hirokazu¹,Fujii Nobutaka¹,Yamamoto Yoshinori²

Affiliation:

1. Faculty of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606, Japan

2. Department of Chemistry, Graduate School of Science, Tohoku University, Aoba, Sendai 980, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo961760o

Reference113 articles.

1. (a) Padwa, A.; Woolhouse, A. D. InComprehensive HeterocyclicChemistry; Katritzky, A. R., Rees, C. W., Eds.; Pergamon Press: Oxford, 1984; Vol. 7, part 5, p 47.

2. Nucleophilic ring opening of aziridine-2-carboxylates with Wittig reagents; an enantioefficient synthesis of unsaturated amino acids