Heterocyclic synthesis via a tandem aza-Wittig reaction/heterocumulene-mediated annulation reaction. New methodology for the preparation of quinazoline derivatives.
- 31 December 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (31) , 3849-3852
- https://doi.org/10.1016/s0040-4039(00)82131-0
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Conjugated carbodiimides: Preparation and thermal cyclization to 2-aminopyridine derivativesTetrahedron Letters, 1988
- 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.Tetrahedron Letters, 1987
- Heterocyclic synthesis via a 1,3-dicyclohexylcarbodiimide-mediated cyclodesulfurative annulation reaction. New methodology for the preparation of guanosine and guanosine-type nucleoside analogsThe Journal of Organic Chemistry, 1986