Diastereoselective Synthesis and Conformational Analysis of (2R)- and (2S)-Fluorostatines: An Approach Based on Organocatalytic Fluorination of a Chiral Aldehyde-Reference-Cited by-同舟云学术

Diastereoselective Synthesis and Conformational Analysis of (2R)- and (2S)-Fluorostatines: An Approach Based on Organocatalytic Fluorination of a Chiral Aldehyde

Published:2016-02-10 Issue:4 Volume:18 Page:662-665
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Hu Xiang-Guo¹²,Lawer Aggie²,Peterson Matthew B.²³,Iranmanesh Hasti²,Ball Graham E.²,Hunter Luke²

Affiliation:

1. National Engineering Research Center for Carbohydrate Synthesis, Jiangxi Normal University, Nanchang 330022, China

2. School of Chemistry, UNSW Australia, Sydney, NSW 2052, Australia

3. Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney, NSW 2109, Australia

Funder

Australian Research Council

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b03592

Reference43 articles.

1. PEPSTATIN, A NEW PEPSIN INHIBITOR PRODUCED BY AGTINOMYGETES

2. The Isolation and Structure Elucidation of Tasiamide B, a 4-Amino-3-hydroxy-5-phenylpentanoic Acid Containing Peptide from the Marine Cyanobacterium Symploca sp.

3. Grassystatins A−C from Marine Cyanobacteria, Potent Cathepsin E Inhibitors That Reduce Antigen Presentation

4. Lower Homologues of Ahpatinin, Aspartic Protease Inhibitors, from a Marine Streptomyces sp.

5. Aspartic Proteinases in Disease: A Structural Perspective

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