O-(Aminosulfonylation) of phenols and an example of slow hydrolytic release-Reference-Cited by-同舟云学术

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O-(Aminosulfonylation) of phenols and an example of slow hydrolytic release

Published:2014-12 Issue:49 Volume:55 Page:6658-6661
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Yang Baocheng,Sun Zhexun,Liu Changzhi,Cui Yan,Guo Zhilei,Ren Yuwei,Lu Zhijian,Knapp Spencer

Funder

Huanghe Science & Technology College

Samos Pharmaceuticals

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. The Organic Chemistry of Drug Design and Drug Action;Silverman,2004

2. Prodrugs: design and clinical applications

3. Prodrugs—from Serendipity to Rational Design

4. Sulfamic Acid and Its N- and O-Substituted Derivatives

5. Sulfamates of various estrogens are prodrugs with increased systemic and reduced hepatic estrogenicity at oral application

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1. Effective C5‐Arylation of Peptide‐Integrated Oxazoles: Almazole D;Advanced Synthesis & Catalysis;2020-12-21

2. Photochemically-Mediated, Nickel-Catalyzed Synthesis of N-(Hetero)aryl Sulfamate Esters;Organic Letters;2019-08-22

3. Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides;RSC Advances;2019

4. Combinatorial Chemistry Online Volume 17, Issue 2, February 2015;Combinatorial Chemistry - an Online Journal;2015-02

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