Heterocyclic synthesis via a tandem aza-Wittig reaction/heterocumulene-mediated annulation reaction. New methodology for the preparation of quinazoline derivatives.-Reference-Cited by-同舟云学术

Heterocyclic synthesis via a tandem aza-Wittig reaction/heterocumulene-mediated annulation reaction. New methodology for the preparation of quinazoline derivatives.

Published:1988-01 Issue:31 Volume:29 Page:3849-3852
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Molina Pedro,Alajarín Mateo,Vidal Angel

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference5 articles.

1. Tandem aza-wittig reaction/electrocyclic ring-closure a facile entry to the synthesis of fused pyrimidines: Preparation of pyrazolo[3,4-d] and 1,2,3-triazolo[4,5-d]pyrimidine derivatives.

2. Conjugated carbodiimides: Preparation and thermal cyclization to 2-aminopyridine derivatives

3. Heterocyclic synthesis via a 1,3-dicyclohexylcarbodiimide-mediated cyclodesulfurative annulation reaction. New methodology for the preparation of guanosine and guanosine-type nucleoside analogs

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