Cycloaddition reactions of thiazolidine derivatives. An approach to the synthesis of new functionalized heterocyclic systems

Authors
Gomez-Monterrey, IM Campiglia, P Mazzoni, O Novellino, E Diurno, MV
Citation
Im. Gomez-monterrey et al., Cycloaddition reactions of thiazolidine derivatives. An approach to the synthesis of new functionalized heterocyclic systems, TETRAHEDR L, 42(33), 2001, pp. 5755-5757
Citations number
16
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
42
Issue
33
Year of publication
2001
Pages
5755 - 5757
Database
ISI
SICI code
0040-4039(20010813)42:33<5755:CROTDA>2.0.ZU;2-8
Abstract
A one-pot procedure for the synthesis of two functionalized tricyclic syste ms having structures of benzo[g]isoquinoline-5,10-dione and dihydrothieno[2 ,3-b]naphto-4,9-dione (DTNQ) is described. These new series were synthesize d from cycloaddition reactions between naphthoquinone and arylthiazolidine derivatives, the latter acting, respectively, as highly reactive N-aryl-ide nedehydroalanine ethyl esters (2-AD) or as amino ester nucleophilic species . (C) 2001 Elsevier Science Ltd. All rights reserved.