Concise approach to the core of englerin A via an organocatalytic [4+3] cycloaddition reaction-Reference-Cited by-同舟云学术

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Concise approach to the core of englerin A via an organocatalytic [4+3] cycloaddition reaction

Published:2011-04 Issue:17 Volume:52 Page:2155-2158
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sun Bing-Feng,Wang Chao-Lei,Ding Rui,Xu Jin-Yi,Lin Guo-Qiang

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

1. Englerin A, a Selective Inhibitor of Renal Cancer Cell Growth, from Phyllanthus engleri

2. Beutler, J. A.; Ratnayake, R.; Covell, D.; Johnson, T. R. WO2009/088854, 2009.

3. Total Synthesis and Absolute Configuration of the Guaiane Sesquiterpene Englerin A

4. Asymmetric, Protecting-Group-Free Total Synthesis of (−)-Englerin A

5. Enantioselective Synthesis of (−)-Englerins A and B

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1. Progress in organocatalytic asymmetric (4+3) cycloadditions for the enantioselective construction of seven-membered rings;Science China Chemistry;2023-02-15

2. Biological Effects of Modifications of the Englerin A Glycolate;ACS Medicinal Chemistry Letters;2022-08-22

3. Enantiomeric Isopulegol as the Chiral Pool in the Total Synthesis of Bioactive Agents;The Chemical Record;2021-09-23

4. Total Synthesis of (−)‐4‐ epi ‐Englerin A;European Journal of Organic Chemistry;2021-06-10

5. Recent applications of asymmetric organocatalytic annulation reactions in natural product synthesis;Chemical Society Reviews;2021

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