Total synthesis of (±)-villosin C and (±)-teuvincenone B-Reference-Cited by-同舟云学术

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Total synthesis of (±)-villosin C and (±)-teuvincenone B

Published:2024 Issue:2 Volume:11 Page:472-476
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Zhou Jin-Xin¹²,Yan Ming-Jie³¹,Shi Xiao-Yu³¹,Wang Yue-Qi³¹,Shen Hong-Yan¹,Mao Xu-Dong¹,Wang Jie¹³²^ORCID

Affiliation:

1. State Key Laboratory of Chemical Biology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China

2. University of Chinese Academy of Sciences, Beijing 100049, China

3. School of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing 210023, China

Abstract

Total synthesis of 17(15 → 16)-abeo-abietane diterpenoids (±)-villosin C and (±)-teuvincenone B was accomplished for the first time in 11 steps.

Funder

National Outstanding Youth Science Fund Project of National Natural Science Foundation of China

Shanghai Institute of Materia Medica, Chinese Academy of Sciences

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO01841E

Reference37 articles.

1. Abietane Diterpenes of the Genus Plectranthus sensu lato

2. Biologically Active Diterpenoids in the Clerodendrum Genus—A Review

3. Chemical and biological evaluation of genus teucrium

4. Rearranged abietane diterpenoids from the root of two Teucrium species

5. Diterpenoide Drüsenfarbstoffe aus Labiaten: 22 neue Coleone und Royleanone ausPlectranthus lanuginosus

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