Catalysis of 3-Pyrrolidinecarboxylic Acid and Related Pyrrolidine Derivatives in Enantioselective anti-Mannich-Type Reactions: Importance of the 3-Acid Group on Pyrrolidine for Stereocontrol-Reference-Cited by-同舟云学术

Catalysis of 3-Pyrrolidinecarboxylic Acid and Related Pyrrolidine Derivatives in Enantioselective anti-Mannich-Type Reactions: Importance of the 3-Acid Group on Pyrrolidine for Stereocontrol

Published:2007-12-29 Issue:3 Volume:130 Page:875-886
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Zhang Haile¹,Mitsumori Susumu¹,Utsumi Naoto¹,Imai Masanori¹,Garcia-Delgado Noemi¹,Mifsud Maria¹,Albertshofer Klaus¹,Cheong Paul Ha-Yeon¹,Houk K. N.¹,Tanaka Fujie¹,Barbas Carlos F.¹

Affiliation:

1. The Skaggs Institute for Chemical Biology and the Departments of Chemistry and Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, and Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja074907%2B

Reference20 articles.

1. anti-Selective Direct Catalytic Asymmetric Mannich-type Reaction of Hydroxyketone Providing β-Amino Alcohols

2. A Highly Enantioselective Amino Acid-Catalyzed Route to Functionalized α-Amino Acids

3. Direct Asymmetric anti-Mannich-Type Reactions Catalyzed by a Designed Amino Acid

4. 3-Pyrrolidinecarboxylic Acid for Direct Catalytic Asymmetric anti-Mannich-Type Reactions of Unmodified Ketones

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