Pd(II)-Catalyzed Regio-, Enantio-, and Diastereoselective 1,4-Addition of Azlactones Formed in Situ From Racemic Unprotected Amino Acids and Acetic Anhydride-Reference-Cited by-同舟云学术

Pd(II)-Catalyzed Regio-, Enantio-, and Diastereoselective 1,4-Addition of Azlactones Formed in Situ From Racemic Unprotected Amino Acids and Acetic Anhydride

Published:2012-11-29 Issue:23 Volume:77 Page:10846-10855
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Weber Manuel¹,Peters René¹

Affiliation:

1. Institut für Organische Chemie, Universität Stuttgart, Pfaffenwaldring 55, D-70569 Stuttgart, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo302177t

Reference61 articles.

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4. Peptidomimetics for Receptor Ligands?Discovery, Development, and Medical Perspectives

5. Synthesis of [alpha-methyltyrosine-4]angiotensin II: studies of its conformation, pressor activity, and mode of enzymatic degradation.

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