Asymmetric Total Synthesis and Determination of the Absolute Configuration of (+)-Srilankenyne via Sequence-Sensitive Halogenations Guided by Conformational Analysis-Reference-Cited by-同舟云学术

Asymmetric Total Synthesis and Determination of the Absolute Configuration of (+)-Srilankenyne via Sequence-Sensitive Halogenations Guided by Conformational Analysis

Published:2021-02-03 Issue:4 Volume:23 Page:1321-1326
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Jang Hongjun¹,Kwak Soo Yeon¹,Lee Dongjoo¹^ORCID,Alegre-Requena Juan V.²,Kim Hyoungsu¹^ORCID,Paton Robert S.²,Kim Deukjoon³^ORCID

Affiliation:

1. College of Pharmacy and Research Institute of Pharmaceutical Science and Technology (RIPST), Ajou University, Suwon 16499, Korea

2. Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523, United States

3. The Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Korea

Funder

National Research Foundation of Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c04303

Reference47 articles.

1. Progress in the Chemistry of Organic Natural Products 101

2. C15 acetogenins from the Laurencia complex: 50 years of research – an overview

3. Halogenated Organic Molecules of Rhodomelaceae Origin: Chemistry and Biology

4. Srilankenyne, a new metabolite from the sea hare Aplysia oculifera

5. Scanlonenyne, a novel halogenated C 15 acetogenin from the red alga Laurencia obtusa in Irish waters

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