Stereoselective synthesis of acyclic (Z)-3-haloallylamines via a multicomponent reaction of propargylic alcohols, TMSX and sulfonamides
Author:
Funder
Science and Technology Commission of Shanghai Municipality
Publisher
Elsevier BV
Reference26 articles.
1. Inhibition of rat aorta semicarbazide-sensitive amine oxidase by 2-phenyl-3-haloallylamines and related compounds
2. Formaldehyde produced endogenously via deamination of methylamine. A potential risk factor for initiation of endothelial injury
3. Inactivation of bovine plasma amine oxidase by haloallylamines
4. Identification and Optimization of Mechanism-Based Fluoroallylamine Inhibitors of Lysyl Oxidase-like 2/3
5. Highly potent propargylamine and allylamine inhibitors of bovine plasma amine oxidase
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