Selective modification of sulfamidate-containing peptides-Reference-Cited by-同舟云学术

Selective modification of sulfamidate-containing peptides

Published:2020 Issue:32 Volume:18 Page:6265-6275
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Mazo Nuria¹²³⁴⁵,Navo Claudio D.⁶⁷⁸⁵^ORCID,Peregrina Jesús M.¹²³⁴⁵^ORCID,Busto Jesús H.¹²³⁴⁵,Jiménez-Osés Gonzalo⁶⁷⁸⁵^ORCID

Affiliation:

1. Departamento de Química

2. Universidad de La Rioja

3. Centro de Investigación en Síntesis Química

4. E-26006 Logroño

5. Spain

6. Center for Cooperative Research in Biosciences (CIC bioGUNE)

7. Basque Research and Technology Alliance (BRTA)

8. 48160 Derio

Abstract

Hybrid peptides whose N-terminal residues are activated in the form of α-methylisoserine cyclic sulfamidates exhibit rich reactivity as electrophiles, allowing site- and stereoselective modifications at different backbone and side chain positions.

Funder

Ministerio de Ciencia e Innovación

Mizutani Foundation for Glycoscience

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB01061H

Reference67 articles.

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3. Thermal Safety and Structure-Related Reactivity Investigation of Five-Membered Cyclic Sulfamidates;Organic Process Research & Development;2022-09-06

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