2015New Journal of ChemistryRequires access

Regioselective nucleophilic aromatic substitution reactions of 5,7-dinitroquinazoline-4-one and 5,7-dinitroquinazoline-4-thione with methylamine: a mechanistic consideration

Amritpal Singh, Neetu Goel

Open publisher page 12 citations

Abstract

Thiocarbonyls, similar to carbonyls, are able to provide regioselective control for the attack of amines at the peri -position of 5,7-dinitroquinazoline-4-thione through intramolecular N–H–SC hydrogen bonding.

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What this paper is about

Thiocarbonyls, similar to carbonyls, are able to provide regioselective control for the attack of amines at the peri -position of 5,7-dinitroquinazoline-4-thione through intramolecular N–H–SC hydrogen bonding.

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OpenAlex reports 12 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Thiocarbonyls, similar to carbonyls, are able to provide regioselective control for the attack of amines at the peri -position of 5,7-dinitroquinazoline-4-thione through intramolecular N–H–SC hydrogen bonding.

Key concepts: Chemistry, Regioselectivity, Intramolecular force, Methylamine, Electrophilic aromatic substitution, Nucleophilic substitution, Substitution reaction, Medicinal chemistry

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Regioselective nucleophilic aromatic substitution reactions of 5,7-dinitroquinazoline-4-one and 5,7-dinitroquinazoline-4-thione with methylamine: a mechanistic consideration — Research Paper | ScholarLens