Enantioselective Total Syntheses of (−)-Caulamidine D and (−)-Isocaulamidine D and Their Absolute Configuration Reassignment-Reference-Cited by-同舟云学术

Enantioselective Total Syntheses of (−)-Caulamidine D and (−)-Isocaulamidine D and Their Absolute Configuration Reassignment

Published:2023-10-04 Issue:41 Volume:145 Page:22335-22340
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Yu Haiyong¹,Zhang Junhao¹,Ma Dongxu¹,Li Xiaotong¹,Xu Tao¹²^ORCID

Affiliation:

1. Molecular Synthesis Center and Key Laboratory of Marine Drugs, MOE, and School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China

2. Laboratory for Marine Drugs and Bioproducts of Marine Natural Products, Laoshan Lab, Qingdao 266237, China

Funder

National Natural Science Foundation of China

Shandong Science Fund for Distinguished Young Scholars

Qingdao Marine Science and Technology Center

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.3c08714

Reference36 articles.

1. Mechanistic considerations of halogenating enzymes

2. Total Synthesis of Aplydactone by a Conformationally Controlled C−H Functionalization

3. Two-Stage Syntheses of Clionastatins A and B

4. Total Syntheses of Aflavazole and 14-Hydroxyaflavinine

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