One-pot synthesis of thiazolidino [3,2-a] pyrimidine derivatives

Article abstract of DOI:10.1080/00397919108016417

Reaction of 2-aminothiazoline with an aromatic aldehyde and an activated methylene group (malonitrile, diethylmalonate or ethylcyanoacetate) gave the title compounds. The structures are unambiguously assigned using spectroscopic data and chemical proofs.

Full text of DOI:10.1080/00397919108016417

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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One-Pot Synthesis of
Thiazolidino [3,2-a] Pyrimidine
Derivatives
Edwige Jeanneau-Nicolle a , Martine Benoit-Guyod a
& Gérard Leclerc a
a Groupe de Pharmacochimie Moléculaire,
Laboratoire de Chimie Organique , UFR de
Pharmacie - Université Joseph Fourier , (Grenoble
I), BP 138, 38240, Meylan-Cedex, France
Published online: 24 Sep 2006.
To cite this article: Edwige Jeanneau-Nicolle , Martine Benoit-Guyod & Gérard
Leclerc (1991) One-Pot Synthesis of Thiazolidino [3,2-a] Pyrimidine Derivatives,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 21:14, 1443-1454, DOI: 10.1080/00397919108016417
To link to this article: http://dx.doi.org/10.1080/00397919108016417
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