Stereoselective Total Synthesis of (−)-Cleistenolide-Reference-Cited by-同舟云学术

Stereoselective Total Synthesis of (−)-Cleistenolide

Published:2010-07-22 Issue:16 Volume:75 Page:5754-5756
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Cai Chao¹²,Liu Jun¹,Du Yuguo¹²,Linhardt Robert J.³

Affiliation:

1. State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China

2. College of Chemistry and Chemical Engineering, Graduate University of Chinese Academy of Sciences, Beijing 100049, China

3. Departments of Chemistry, Biology, and Chemical and Biological Engineering, Rensselaer Polytechnic Institute, Troy, New York 12180

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo101059e

Reference20 articles.

1. Annonaceous Acetogenins: Recent Progress

2. Cyclohexene epoxides, (+)-pandoxide, (+)β-senepoxide and (−)-pipoxide, from Uvaria pandensis

3. Tanzanene, a spiro benzopyranyl sesquiterpene from Uvaria tanzaniae Verdc

4. Constituents from Miliusa balansae (Annonaceae)

5. Bioactive Constituents of the Stem Bark of Mitrephora glabra

Cited by 27 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis and antiproliferative activity of (−)-cleistenolide, (6S)-cleistenolide and 4-substituted cleistenolide analogues;Bioorganic & Medicinal Chemistry;2024-09

2. Synthesis and antimicrobial activity of (−)-cleistenolide and analogues;Bioorganic Chemistry;2021-01

3. Synthetic Studies toward (−)-Cleistenolide: Highly Stereoselective Synthesis of New γ-Lactone Subunits;Journal of the Brazilian Chemical Society;2021

4. Miscellaneous Reactions;Applied Organic Chemistry;2020-12-11

5. Synthesis, antiproliferative activity and SAR analysis of (−)-cleistenolide and analogues;European Journal of Medicinal Chemistry;2020-09