Enantioselective Total Syntheses of Omuralide, 7-epi-Omuralide, and (+)-Lactacystin-Reference-Cited by-同舟云学术

Enantioselective Total Syntheses of Omuralide, 7-epi-Omuralide, and (+)-Lactacystin

Published:2008-02-21 Issue:6 Volume:73 Page:2041-2051
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hayes Christopher J.¹,Sherlock Alexandra E.¹,Green Martin P.¹,Wilson Claire¹,Blake Alexander J.¹,Selby Matthew D.¹,Prodger Jeremy C.¹

Affiliation:

1. School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK, Pfizer Global Research and Development, Ramsgate Road, Sandwich, Kent, CT13 9NJ, UK, and GlaxoSmithKline, Medicines Research Centre, Gunnels Wood Road, Stevenage, Hertfordshire SG1 2NY, UK

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo7027695

Reference70 articles.

1. Lactacystin, a novel microbial metabolite, induces neuritogenesis of neuroblastoma cells.

2. Inhibition of Proteasome Activities and Subunit-Specific Amino-Terminal Threonine Modification by Lactacystin

3. Nitrone [2+3]-Cycloadditions in Stereocontrolled Synthesis of a Potent Proteasome Inhibitor: (−)-Omuralide

4. Stereogenic Evolution ofclasto-Lactacystin β-Lactone fromL-Serine

5. New Entry to Convertible Isocyanides for the Ugi Reaction and Its Application to the Stereocontrolled Formal Total Synthesis of the Proteasome Inhibitor Omuralide

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