General-buffer catalysis of the reaction of N-(hydroxymethyl)benzamide: a new pathway for the aqueous reaction of carbinolamides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference41 articles.
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Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Carbinol Derivatives of N ‐(α‐Hydroxybenzyl)benzamide: Acid and Base‐Dependent Kinetics in Water and the Mechanistic Implications for Carbinolamide Reactivity;ChemistrySelect;2021-10-18
2. N-(Hydroxybenzyl)benzamide Derivatives: Aqueous pH-Dependent Kinetics and Mechanistic Implications for the Aqueous Reactivity of Carbinolamides;The Journal of Organic Chemistry;2019-12-12
3. Synthesis of [3-N-11C-methyl]temozolomide viain situactivation of 3-N-hydroxymethyl temozolomide and alkylation with [11C]methyl iodide;Journal of Labelled Compounds and Radiopharmaceuticals;2015-02-17
4. Solvent-free synthesis of monoacylaminals from the reaction of amides and aminals as precursors in carbinolamide synthesis;Tetrahedron Letters;2010-11
5. Rapid amidic hydrolysis: a competitive reaction pathway under basic conditions for N-(hydroxymethyl)benzamide derivatives bearing electron-donating groups;Tetrahedron Letters;2009-12
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