Regiospecific substitution of the 4-nitro group in 3-amino-4,6-dinitrobenzo[b]thiophene-2-carboxylates: unexpected activating effect of the amino group-Reference-Cited by-同舟云学术

Regiospecific substitution of the 4-nitro group in 3-amino-4,6-dinitrobenzo[b]thiophene-2-carboxylates: unexpected activating effect of the amino group

Published:2001-11 Issue:48 Volume:42 Page:8539-8541
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Shevelev Svyatoslav A,Dalinger Igor L,Cherkasova Tatyana I

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference5 articles.

1. Formation of 2,4,6-trinitrobenzonitrile and 4-chloro-5,7-dinitro-2-(2,4,6-trinitrophenyl)quinazoline 1-oxide by the action of nitrosyl chloride on 2,4,6-trinitrotoluene

2. Regioselectivity of the substitution for the nitro group in 2,4,6-trinitrobenzonitrile under the action of thiols. The synthesis of 4,6-dinitro derivatives of benzoannelated sulfur-containing heterocycles

3. A survey of Hammett substituent constants and resonance and field parameters

4. Regiospecificity in nucleophilic displacement of aromatic nitro-groups

5. Relationship of aromatic nitro group torsion angles with oxygen-17 chemical shift data

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