New entry to the synthesis of clerodane diterpenes. The first enantioselective syntheses of 7-oxo-kolavenic acid and methyl solidagonate-Reference-Cited by-同舟云学术

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New entry to the synthesis of clerodane diterpenes. The first enantioselective syntheses of 7-oxo-kolavenic acid and methyl solidagonate

Published:2001-09 Issue:39 Volume:57 Page:8243-8256
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Kato Michiharu,Kosugi Hiroshi,Ichiyanagi Tsuyoshi,Hagiwara Hisahiro,Kodaira Ariko,Kusakari Takashi,Suzuki Takao,Ando Minako,Lee Jasmine,Drechsel Peter,Vogler Bernhard

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Clerodane diterpenoids

2. The crystal structure of 3-epicaryoptin and the reversal of the currently accepted absolute configuration of clerodin

3. Isolation and characterization of terpentecin, a new antitumor antibiotic.

Cited by 11 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. Carbonyl and Imine Ene Reactions, Prins Reactions and Cyclizations, and Lewis Acid–Catalyzed Carbonyl Olefin Metathesis;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2023

2. New clerodane diterpenoids from Solidago altissima and stereochemical elucidation via 13C NMR chemical shift analysis;Tetrahedron;2022-03

3. Total synthesis of (+)-ent-vetiverianine a via Lewis acid-mediated cyclization;Organic Chemistry Frontiers;2022

4. Total Syntheses of Clerodane Diterpenoids—A Review;Natural Product Communications;2019-06

5. Sequential Hydrozirconation/Cyclization of Dienes, a New Route toward Trans 2-Substituted Vinylcyclopentanes;Organic Letters;2014-02-26

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