Asymmetric Total Synthesis of (+)-Waihoensene-Reference-Cited by-同舟云学术

Asymmetric Total Synthesis of (+)-Waihoensene

Published:2020-03-23 Issue:14 Volume:142 Page:6511-6515
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Qu Yongzheng¹,Wang Zheyuan¹,Zhang Zhongchao¹,Zhang Wendou¹,Huang Jun¹,Yang Zhen¹²³^ORCID

Affiliation:

1. Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen, 518055, China

2. 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

3. Shenzhen Bay Laboratory, Shenzhen 518055, China

Funder

National 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.0c02143

Reference62 articles.

1. Synthesis of Polyquinane Natural Products: An Update

2. Linear Triquinane Sesquiterpenoids: Their Isolation, Structures, Biological Activities, and Chemical Synthesis

3. Waihoensene. A new laurenene-related diterpene from Podocarpus totara var waihoensis

4. Synthetic Strategies toward Natural Products Containing Contiguous Stereogenic Quaternary Carbon Atoms

5. A New Tandem Route to Angular Tetraquinanes. Synthesis of the Waihoensene Ring System

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