Chemoenzymatic Oxidation of Labdane and Formal Synthesis of Nimbolide-Reference-Cited by-同舟云学术

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Chemoenzymatic Oxidation of Labdane and Formal Synthesis of Nimbolide

Published:2024-09-14 Issue: Volume: Page:
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Liu Xiaotao¹,Xu Yaoyao¹,Li Lingling²,Li Jian¹^ORCID

Affiliation:

1. Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs and Zhangjiang Institute for Advanced Study, Shanghai Jiao Tong University, Shanghai 200240, China

2. Instrumental Analysis Center, Shanghai Jiao Tong University, Shanghai 200240, China

Funder

National Key Research and Development Program of China

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.4c07956

Reference59 articles.

1. C–H functionalization logic in total synthesis

2. Advancing the Logic of Chemical Synthesis: C−H Activation as Strategic and Tactical Disconnections for C−C Bond Construction

3. Biocatalytic retrosynthesis

4. Terpenoids As Therapeutic Drugs and Pharmaceutical Agents

5. Structures and stereochemistry of new labdane diterpiniods from coleus forskohlii briq.

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