Enantioselective Synthesis of Macrolide Pheromones, (5Z, 13S)-5-Tetradecen-13-olide and (9R)-Decan-9-olide, by Using Mn-Salen Catalyzed Asymmetric Epoxidation as a Key Step-Reference-Cited by-同舟云学术

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Enantioselective Synthesis of Macrolide Pheromones, (5Z, 13S)-5-Tetradecen-13-olide and (9R)-Decan-9-olide, by Using Mn-Salen Catalyzed Asymmetric Epoxidation as a Key Step

Published:1995-05 Issue:05 Volume:1995 Page:407-408
ISSN:0936-5214
Container-title:Synlett
language:
Short-container-title:Synlett

Author:

Hamada Tetsuya,Daikai Kazuhiro,Irie Ryo,Katsuki Tsutomu

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-1995-5001.pdf

Cited by 14 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. Continuous Flow Z ‐Stereoselective Olefin Metathesis: Development and Applications in the Synthesis of Pheromones and Macrocyclic Odorant Molecules**;Angewandte Chemie International Edition;2021-08

2. Continuous Flow Z ‐Stereoselective Olefin Metathesis: Development and Applications in the Synthesis of Pheromones and Macrocyclic Odorant Molecules**;Angewandte Chemie;2021-08

3. Identification, synthesis and mass spectrometry of a macrolide from the African reed frog Hyperolius cinnamomeoventris;Beilstein Journal of Organic Chemistry;2016-12-13

4. Katsuki Catalysts for Asymmetric Oxidation: Design Concepts, Serendipities for Breakthroughs, and Applications;Chemistry Letters;2015-10-05

5. 8.29 Reduction of Epoxides;Comprehensive Organic Synthesis II;2014

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