Stereochemistry of cleistanthane diterpenoid glucosides from Phyllanthus emblica-Reference-Cited by-同舟云学术

Stereochemistry of cleistanthane diterpenoid glucosides from Phyllanthus emblica

Published:2015 Issue:37 Volume:5 Page:29098-29107
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Lv Jun-Jiang¹²³⁴⁵,Yu Shan¹²³⁴⁵,Xin Ying¹²³⁴⁵,Zhu Hong-Tao¹²³⁴⁵,Wang Dong¹²³⁴⁵,Cheng Rong-Rong¹²³⁴⁵,Yang Chong-Ren¹²³⁴⁵,Xu Min¹²³⁴⁵,Zhang Ying-Jun¹²³⁴⁵

Affiliation:

1. State Key Laboratory of Phytochemistry and Plant Resources in West China

2. Kunming Institute of Botany

3. Chinese Academy of Sciences

4. Kunming 650201

5. People’s Republic of China

Abstract

Theoretical calculated electronic circular dichroism and Mosher’s method were applied to elucidate the stereochemistry of cleistanthane diterpenoids.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C4RA16624H

Reference22 articles.

1. Pimarane and cleistanthane diterpenes from velloziaceae: absolute configuration and biomimetic conversion

2. Cleistanthol, a novel diterpene from Cleistanthus schlechteri(Euphorbiaceae)

3. Pimarane diterpenes from Cleistanthus schlechteri

4. Abietane Diterpenoids from Clerodendrum bungei

5. Abietane diterpenoids synthesized by suspension-cultured cells of Cephalotaxus fortunei

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