Synthesis of Disubstituted 6-Chloro-5-methyl-4H-1,4-benzothiazines: Novel Heterocycles

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Title:Synthesis of Disubstituted 6-Chloro-5-methyl-4H-1,4-benzothiazines: Novel Heterocycles
Creators:
Rathore, Ram K.
Gupta, Radha R.
Journal or Publication Title:
Collection of Czechoslovak Chemical Communications, 60, 12, pp. 2209-2212

Abstract

<p>2-Amino-4-chloro-3-methylbenzenethiol in the form of dimer condensed with 8 β-diketones or β-ketoesters to form an enaminoketone or ester intermediate which underwent spontaneous oxidative cyclization to form 6-chloro-5-methyl-2,3-disubstituted 4<i>H</i>-1,4-benzothiazines.

Title:Synthesis of Disubstituted 6-Chloro-5-methyl-4H-1,4-benzothiazines: Novel Heterocycles
Creators:
Rathore, Ram K.
Gupta, Radha R.
Divisions:Life and Chemical Sciences > Institute of Organic Chemistry and Biochemistry > Collection of Czechoslovak Chemical Communications
Journal or Publication Title:Collection of Czechoslovak Chemical Communications
Volume:60
Number:12
Page Range:pp. 2209-2212
ISSN:0010-0765
E-ISSN:1212-6950
Publisher:Institute of Organic Chemistry and Biochemistry
Related URLs:
URLURL Type
http://dx.doi.org/10.1135/cccc19952209UNSPECIFIED
ID Code:910
Item Type:Article
Deposited On:06 Feb 2009 17:04
Last Modified:06 Feb 2009 16:05

Citation

Rathore, Ram K.; Gupta, Radha R. (1995) Synthesis of Disubstituted 6-Chloro-5-methyl-4H-1,4-benzothiazines: Novel Heterocycles. Collection of Czechoslovak Chemical Communications, 60 (12). pp. 2209-2212. ISSN 0010-0765

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