Regio- and Stereoselective Synthesis of (E)-Alkene trans-Xaa-Pro Dipeptide Mimetics Utilizing Organocopper-Mediated Anti-SN2‘ Reactions-Reference-Cited by-同舟云学术

Regio- and Stereoselective Synthesis of (E)-Alkene trans-Xaa-Pro Dipeptide Mimetics Utilizing Organocopper-Mediated Anti-SN2‘ Reactions

Published:2002-08-01 Issue:17 Volume:67 Page:6152-6161
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Otaka Akira¹,Katagiri Fumihiko¹,Kinoshita Takayoshi¹,Odagaki Yoshihiko¹,Oishi Shinya¹,Tamamura Hirokazu¹,Hamanaka Nobuyuki¹,Fujii Nobutaka¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan, Fujisawa Pharmaceutical Co., Ltd., Kashima, Yodogawa-ku, Osaka 532-8514, Japan, and Minase Research Institute, Ono Pharmaceutical Co. Ltd., Mishima-gun, Osaka 618-8585, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo025922u

Reference82 articles.

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3. An explanation for the rare occurrence of cis peptide units in proteins and polypeptides

4. Conformational energy studies of linear dipeptides H-X-L-Pro-OH

5. Nmr studies of the rates of prolinecis-transisomerization in oligopeptides

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