Total syntheses of seminolipid and its analogues by using 2,6-bis(trifluoromethyl)phenylboronic acid as protective reagent-Reference-Cited by-同舟云学术

Total syntheses of seminolipid and its analogues by using 2,6-bis(trifluoromethyl)phenylboronic acid as protective reagent

Published:2019 Issue:31 Volume:17 Page:7325-7329
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Shimada Naoyuki¹²³⁴^ORCID,Fukuhara Kenji¹²³⁴,Urata Sari¹²³⁴,Makino Kazuishi¹²³⁴^ORCID

Affiliation:

1. Department of Pharmaceutical Sciences

2. Kitasato University

3. Tokyo 108-8641

4. Japan

Abstract

Total synthesis of seminolipid was accomplished via regioselective protection using 2,6-bis(trifluoromethyl)phenylboronic acid followed by regioselective trichloroethyl-protected sulfation as key steps.

Funder

Japan Society for the Promotion of Science

Japan Science Society

Kitasato University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB01445D

Reference67 articles.

1. Chemistry and functional distribution of sulfoglycolipids

2. Properties, metabolism and roles of sulfogalactosylglycerolipid in male reproduction

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