Epoc group: transformable protecting group with gold(iii)-catalyzed fluorene formation-Reference-Cited by-同舟云学术

Epoc group: transformable protecting group with gold(iii)-catalyzed fluorene formation

Published:2021 Issue:32 Volume:12 Page:10703-10709
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Yamamoto Tomoya¹^ORCID,Chang Tsung-Che¹,Tanaka Katsunori¹²³^ORCID

Affiliation:

1. Biofunctional Synthetic Chemistry Laboratory, RIKEN Cluster for Pioneering Research, 2-1 Hirosawa, Wako-shi, Saitama, 351-0198, Japan

2. Department of Chemical Science and Engineering, School of Materials and Chemical Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8552, Japan

3. Biofunctional Chemistry Laboratory, Alexander Butlerov Institute of Chemistry, Kazan Federal University, 18 Kremlyovskaya Street, 420008, Kazan, Russian Federation

Abstract

A protecting group removable with gold(iii)-catalyzed fluorene formation and the subsequent addition of piperidine was developed.

Funder

RIKEN

Astellas Foundation for Research on Metabolic Disorders

Mizutani Foundation for Glycoscience

Japan Agency for Medical Research and Development

Kazan Federal University

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/SC/D1SC03125B

Reference35 articles.

1. 9-Fluorenylmethoxycarbonyl amino-protecting group

2. SOLID-PHASE PEPTIDE SYNTHESIS USING MILD BASE CLEAVAGE OF NαFLUORENYLMETHYLOXYCARBONYLAMINO ACIDS, EXEMPLIFIED BY A SYNTHESIS OF DIHYDROSOMATOSTATIN

3. A mild procedure for solid phase peptide synthesis: use of fluorenylmethoxycarbonylamino-acids

4. Streamlined access to conjugation-ready glycans by automated synthesis

5. The Logic of Automated Glycan Assembly

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