A Convenient Synthesis of N, N, N'-Trisubstituted Ethylenediamine Derivatives From 2-Methyl-2-imidazoline
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397910008086970
Reference9 articles.
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2. Alkaline hydrolysis of 1,2,3-trisubstituted cyclic amidinium salts. Kinetic study of N → N′ acyl migration in alkaline solution in an ethylenediamine derivative
3. Synthesis and hydrolysis of substituted imidazolinium salts. Behaviour of the degradation products on varyingpH
4. Reduction of substituted 1H-4,5-dihydroimidazolium salts
5. Providing one-carbon units for biological methylations: mechanistic studies on serine hydroxymethyltransferase, methylenetetrahydrofolate reductase, and methyltetrahydrofolate-homocysteine methyltransferase
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1. Ring-opening reactions of 2-imidazolines and their applications;Advances in Heterocyclic Chemistry;2020
2. Biomimetic Synthesis of Benzimidazoles, Benzoxazoles, and Benzothiadazole via the Group Transfer of Tetrahydrofolate Models;Current Organic Synthesis;2014-10-23
3. Groups Transfer Reaction of Imidazolinium Salts as Tetrahydrofolate Model Compounds;CHEM J CHINESE U;2012
4. ChemInform Abstract: A Convenient Synthesis of N,N,N′-Trisubstituted Ethylenediamine Derivatives from 2-Methyl-2-imidazoline.;ChemInform;2010-05-31
5. Imidazoles;Comprehensive Heterocyclic Chemistry III;2008
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