Highly stereocontrolled total synthesis of secodolastane diterpenoid isolinearol-Reference-Cited by-同舟云学术

Highly stereocontrolled total synthesis of secodolastane diterpenoid isolinearol

Published:2020 Issue:37 Volume:18 Page:7316-7320
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Kobayashi Toyoharu¹²³⁴^ORCID,Tomita Yui¹²³⁴,Kawamoto Yuichiro¹²³⁴^ORCID,Ito Hisanaka¹²³⁴

Affiliation:

1. School of Life Sciences

2. Tokyo University of Pharmacy and Life Sciences

3. Tokyo 192-0392

4. Japan

Abstract

The first total synthesis of the secodolastane diterpenoid isolinearol in both racemic and enantioenriched forms has been achieved with high stereoselectively.

Funder

Japan Society for the Promotion of Science

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB01430C

Reference23 articles.

1. Diterpenes from the Marine Algae of the Genus Dictyota

2. What are and where are the bioactive terpenoids metabolites from Dictyotaceae (Phaeophyceae)

3. Dolastane and Secodolastane Diterpenes from the Marine Brown Alga, Dictyota cericornis

4. Marine Natural Products, XIV. Secodolastane Diterpenoids of Dictyota indica from the Arabian Sea

5. Dolastane diterpenes from Canistrocarpus cervicornis and their effects in modulation of drug resistance in Staphylococcus aureus

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