Asymmetric Total Synthesis of (−)-Spirochensilide A-Reference-Cited by-同舟云学术

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Asymmetric Total Synthesis of (−)-Spirochensilide A

Published:2020-04-14 Issue:18 Volume:142 Page:8116-8121
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Liang Xin-Ting¹,Chen Jia-Hua¹,Yang Zhen¹²³^ORCID

Affiliation:

1. Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education and Beijing National Laboratory for Molecular Science, and Peking-Tsinghua Center for Life Sciences, Peking University, Beijing, 100871, China

2. State Key Laboratory of Chemical Oncogenomics and Key Laboratory of Chemical Genomics, Peking University Shenzhen Graduate School, Shenzhen 518055, China

3. Shenzhen Wan Laboratory, Shenzhen, 518055, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.0c02522

Reference75 articles.

1. Spirochensilides A and B, Two New Rearranged Triterpenoids from Abies chensiensis

2. Hot off the press

3. Kansuinone, a novel euphane-type triterpene from Euphorbia kansui

4. An unusual lanostane-type triterpenoid, spiroinonotsuoxodiol, and other triterpenoids from Inonotus obliquus

5. Eight Pairs of Epimeric Triterpenoids Involving a Characteristic Spiro-E/F Ring from Abies faxoniana

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