Regioselective N-alkylation of 2-aminobenzylamine via chelation to 9-BBN
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Selective Syntheses of N-Monoalkyl and N,N‘-Dialkyl Derivatives of 1,8-Diaminonaphthalene−9-BBN as an Activating and Directing Group
2. 3,4-Dihydro-2(1H)-quinazolinones
3. Cyclic guanidines. IX. Synthesis of 2-amino-3,4-dihydroquinazolines as blood platelet aggregation inhibitors.
4. Synthesis and anticonvulsant activity of 3-alkyl-3,4-dihydro-2(1H)-quinazolinones
5. Cyclized Substituted Thioureas I. Preparation of Some 3-Substituted 1,2,3,4-Tetrahydroquinazoline-2-thiones and Their Intermediates
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1. Synthesis of dihydroquinazolines from 2-aminobenzylamine: N3-aryl derivatives with electron-withdrawing groups;Beilstein Journal of Organic Chemistry;2018-09-26
2. Selective Three-Component Coupling for CO2 Chemical Fixation to Boron Guanidinato Compounds;Inorganic Chemistry;2018-06-27
3. Syntheses of 3,4- and 1,4-dihydroquinazolines from 2-aminobenzylamine;Beilstein Journal of Organic Chemistry;2017-07-27
4. Quinazolinones, Quinazolinthiones, and Quinazolinimines as Nitric Oxide Synthase Inhibitors: Synthetic Study and Biological Evaluation;Archiv der Pharmazie;2016-06-21
5. Iron and Manganese Catalysts for the Selective Functionalization of Arene C(sp2 )−H Bonds by Carbene Insertion;Angewandte Chemie International Edition;2016-04-18
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