Rhodium(III)-Catalyzed Kinetic Resolution of Racemic 1,6-Dienes via Asymmetric Borylative Cyclization-Reference-Cited by-同舟云学术

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Rhodium(III)-Catalyzed Kinetic Resolution of Racemic 1,6-Dienes via Asymmetric Borylative Cyclization

Published:2020-04-10 Issue:9 Volume:22 Page:3661-3666
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhang Jun-Li¹,Gao Dingding¹^ORCID,Tan Yun-Xuan²^ORCID,He Cheng-Yu²,Peng Pei-Ying¹,Lin Guo-Qiang¹²,Li Qing-Hua¹^ORCID,Tian Ping¹²^ORCID

Affiliation:

1. The Research Center of Chiral Drugs, Innovation Research Institute of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Shanghai 201203, China

2. CAS Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China

Funder

China Postdoctoral Science Foundation

Shanghai Municipal Education Commission

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Chinese Academy of Sciences

Shanghai Municipality

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c01156

Reference67 articles.

1. Melodinines M–U, Cytotoxic Alkaloids from Melodinus suaveolens

2. Chemical constituents of Melodinus hemsleyanus diels

3. Four New Jacaranone Analogs from the Fruits of a Beibu Gulf Mangrove Avicennia marina

4. JBIR-124: a novel antioxidative agent from a marine sponge-derived fungus Penicillium citrinum SpI080624G1f01

5. Comparisons of Hydroperoxide Isomerase and Monooxygenase Activities of Cytochrome P450 for Conversions of Allylic Hydroperoxides and Alcohols to Epoxyalcohols and Diols: Probing Substrate Reorientation in the Active Site

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