Enantioselective total synthesis of (+)-ieodomycin A, (+)-ieodomycin B, and their three stereoisomers-Reference-Cited by-同舟云学术

Enantioselective total synthesis of (+)-ieodomycin A, (+)-ieodomycin B, and their three stereoisomers

Published:2020 Issue:45 Volume:18 Page:9227-9230
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Choi Du-Bong¹²³⁴⁵,Choi Hansol¹²³⁴,Lee Jihoon¹²³⁴⁶,Lee Yeon-Ju¹²³⁴⁶,Lee Hyi-Seung¹²³⁴⁶,Joo Jung Min⁵⁷³⁴^ORCID,Lee Jong Seok¹²³⁴⁶^ORCID

Affiliation:

1. Marine Natural Products Chemistry Laboratory

2. Korea Institute of Ocean Science and Technology (KIOST)

3. Busan

4. Republic of Korea

5. Department of Chemistry and Chemistry Institute for Functional Materials

6. Department of Applied Ocean Science

7. Pusan National University

Abstract

Enantioselective routes for the total synthesis of ieodomycins A & B, and three stereochemical analogues of ieodomycin B via a late-stage elaboration of the side chain.

Funder

Korea Institute of Ocean Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB02107E

Reference30 articles.

1. F. Pietra , J. E.Baldwin and R. M.Williams , Biodiversity and Natural Product Diversity , Elsevier Science , 2002

2. What Is Marine Biodiversity? Towards Common Concepts and Their Implications for Assessing Biodiversity Status

3. Advanced tools in marine natural drug discovery

4. Lessons from the Past and Charting the Future of Marine Natural Products Drug Discovery and Chemical Biology

5. Marine Natural Products in Medicinal Chemistry

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