Efficient and Highly Stereoselective Syntheses of (+)-proto-Quercitol and (−)-gala-Quercitol Starting from the Naturally Abundant (−)-Shikimic Acid-Reference-Cited by-同舟云学术

Efficient and Highly Stereoselective Syntheses of (+)-proto-Quercitol and (−)-gala-Quercitol Starting from the Naturally Abundant (−)-Shikimic Acid

Published:2020-01-21 Issue:4 Volume:5 Page:1813-1821
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Zhu Xing-Liang¹,Wang Lei¹,Luo Yong-Qiang¹,He Yun-Gang¹,Li Feng-Lei¹,Sun Mian-Mian¹,Liu Shi-Ling²,Shi Xiao-Xin¹^ORCID

Affiliation:

1. Shanghai Key Laboratory of Chemical Biology and Department of Pharmaceutical Engineering, School of Pharmacy, East China University of Science and Technology, 130 Mei-Long Road, Shanghai 200237, P. R. China

2. Shanghai Qingping Pharmaceutical Co. Ltd., 397 Zhaojiang Road, Baihe Town, Qingpu District, Shanghai 201710, P. R. China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acsomega.9b02986

Reference70 articles.

1. Synthesis of Two New Quercitol (Deoxyinositol) Stereoisomers. Nuclear Magnetic Resonance and Optical Rotatory Configurational Proofs1,2

2. Quercitol: From a Taxonomic Marker of the Genus Quercus to a Versatile Chiral Building Block of Antidiabetic Agents

3. Stereoselective syntheses of racemic quercitols and bromoquercitols starting from cyclohexa-1,4-diene: gala-, epi-, muco-, and neo-quercitol

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