2,4-Diamino-1-thia-3-azabutadienes, intermediates in heterocyclic synthesis

Article abstract of DOI:10.1080/10426500008044998

2,4-Diamino-1-thia-3-azabutadienes 1 were studied. Methylation occured at sulfur and acylation at nitrogen hound to the 2 position. Alkylation by α-bromoketones gave rise to 2-amino-5-acylthiazoles. Upon treatment with acrylic dienophiles compounds 1 reac

Full text of DOI:10.1080/10426500008044998

Phosphorus, Sulfur, and Silicon and the Related Elements
ISSN: 1042-6507 (Print) 1563-5325 (Online) Journal homepage: http://www.tandfonline.com/loi/gpss20
2,4-DIAMINO-1-THIA-3-AZABUTADIENES,
INTERMEDIATES IN HETEROCYCLIC SYNTHESIS
C. Friot , A. Reliquet , F. Reliquet & J. C. Meslin
To cite this article: C. Friot , A. Reliquet , F. Reliquet & J. C. Meslin (2000) 2,4-DIAMINO-1-THIA-3-
AZABUTADIENES, INTERMEDIATES IN HETEROCYCLIC SYNTHESIS, Phosphorus, Sulfur, and
Silicon and the Related Elements, 156:1, 135-149, DOI: 10.1080/10426500008044998
To link to this article: http://dx.doi.org/10.1080/10426500008044998
Published online: 04 Oct 2006.
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Date: 20 December 2015, At: 19:05