Differential Use of Anhydropyranosides for Enantiopure Routes to Bis-γ-butyrolactones: A New Approach to the Frameworks of Antibiotic and Anticancer Agents Isoavenaciolide and Ethisolide-Reference-Cited by-同舟云学术

Differential Use of Anhydropyranosides for Enantiopure Routes to Bis-γ-butyrolactones: A New Approach to the Frameworks of Antibiotic and Anticancer Agents Isoavenaciolide and Ethisolide

Published:2009-05-21 Issue:13 Volume:74 Page:4690-4696
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Al-Tel Taleb H.¹,Al-Qawasmeh Raed A.¹,Sabri Salim S.¹,Voelter Wolfgang¹

Affiliation:

1. College of Pharmacy, University of Sharjah, P.O. Box 27272, Sharjah, UAE, Chemistry Department, University of Jordan, Amman, Jordan, and Physiologisch-Chemisches Institut der Universität Tübingen, Hoppe-Seyler Strasse 4, D-72076 Tübingen, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo900192a

Reference36 articles.

1. Synthesis and Conformational and Biological Aspects of Carbasugars

2. Carbohydrate-Based Mimetics in Drug Design: Sugar Amino Acids and Carbohydrate Scaffolds

3. 4-Isoavenaciolide covalently binds and inhibits VHR, a dual-specificity phosphatase

4. SYNTHESES OF AVENACIOLIDE AND RELATEDbisLACTONES. A REVIEW

5. Synthesis of bis-.gamma.-lactones from "diacetone glucose". 4. Optically active avenaciolide and isoavenaciolide

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