Total synthesis of thioamycolamide A via a biomimetic route-Reference-Cited by-同舟云学术

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Total synthesis of thioamycolamide A via a biomimetic route

Published:2020 Issue:41 Volume:18 Page:8366-8370
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Pan Chengqian¹²³⁴⁵,Kuranaga Takefumi¹²³⁴⁵,Kakeya Hideaki¹²³⁴⁵^ORCID

Affiliation:

1. Department of System Chemotherapy and Molecular Sciences

2. Division of Bioinformatics and Chemical Genomics

3. Graduate School of Pharmaceutical Sciences

4. Kyoto University

5. Kyoto 606-8501

Abstract

A concise total synthesis of thioamycolamide A was accomplished as a key step of thio-Michael addition via a biomimetic route.

Funder

Ministry of Education, Culture, Sports, Science and Technology

Japan Agency for Medical Research and Development

Daiichi-Sankyo

Takeda Science Foundation

Tokyo Biochemical Research Foundation

China Scholarship Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB01942A

Reference37 articles.

1. Enzymatic Carbon–Sulfur Bond Formation in Natural Product Biosynthesis

2. Construction of sulfur-containing moieties in the total synthesis of natural products

3. Bioinformatic Expansion and Discovery of Thiopeptide Antibiotics

4. Chlorocatechelins A and B from Streptomyces sp.: New Siderophores Containing Chlorinated Catecholate Groups and an Acylguanidine Structure

5. Isolation, Structure Elucidation, and Total Synthesis of Tryptopeptins A and B, New TGF-β Signaling Modulators from Streptomyces sp.

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3. Synthesis of the Alkylsulfonate Metabolites Cysteinolic Acid, 3-Amino-2-hydroxypropanesulfonate, and 2,3-Dihydroxypropanesulfonate;The Journal of Organic Chemistry;2022-02-24

4. Total synthesis of thioamycolamide A using diastereoselective sulfa-Michael addition as the key step;Organic Chemistry Frontiers;2022

5. Synthesis and Absolute Configuration of ((2R,3R,6S)-3-Hydroxy-6-(naphthalen-2-ylthio)-3,6-dihydro-2H-pyran-2-yl) methyl Pivalate;CHINESE J STRUC CHEM;2021

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