Degradation of 2,2′-dihalodiethyl sulfides(mustards) by N,N-dichloro-4- methylbenzenesulphonamide in aprotic medium
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Decontamination of chemical warfare agents
2. Rapid deactivation of mustard via microemulsion technology
3. A comparison of the oxidative reactivities of mustard (2,2'-dichlorodiethyl sulfide) and bivalent sulfides
4. Kinetics and mechanism of the hydrolysis of 2-chloroethyl sulfides
5. Sulfilimine. I. Synthesis and Formation Mechanism
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1. Copper(I)-catalysed site-selective C(sp3)–H bond chlorination of ketones, (E)-enones and alkylbenzenes by dichloramine-T;Nature Communications;2021-07-01
2. N,N-Dichloro-4-methylbenzenesulfonamide [Dichloramine-T];Encyclopedia of Reagents for Organic Synthesis;2013-04-22
3. N, N-Dichlorourethane: An Efficient Decontaminating Reagent for Sulfur Mustard, a Chemical Warfare Agent;Industrial & Engineering Chemistry Research;2013-03-20
4. N,N-Dichlorovaleramide: An Efficient Decontaminating Reagent for Sulfur Mustard;Industrial & Engineering Chemistry Research;2012-04-13
5. Preparation of N, N-dichloropolystyrene sulfonamide nanofiber as a regenerable self-decontaminating material for protection against chemical warfare agents;INT J NANO DIMENS;2012
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