Regio- and stereoselective alkoxycarbonylmethylenation of partially saturated heterobicyclic compounds: First synthesis of 2-substituted quinazoline-8-acetic acid esters

Article abstract of DOI:10.1080/00397919808005102

The three-step synthesis of 2-substituted quinazol-8-yl acetates is described, introducing a completely new method for the regio- and stereoselective alkoxycarbonylmethylenation of tetrahydroquinazolines.

Full text of DOI:10.1080/00397919808005102

Synthetic Communications
ISSN: 0039-7911 (Print) 1532-2432 (Online) Journal homepage: http://www.tandfonline.com/loi/lsyc20
Regio- and Stereoselective
Alkoxycarbonylmethylenation of Partially
Saturated Heterobicyclic Compounds: First
Synthesis of 2-Substituted Quinazoline-8-acetic
Acid Esters
Albrecht Zumbrunn , Clemens Lamberth & Fritz Schaub
To cite this article: Albrecht Zumbrunn , Clemens Lamberth & Fritz Schaub (1998) Regio- and
Stereoselective Alkoxycarbonylmethylenation of Partially Saturated Heterobicyclic Compounds:
First Synthesis of 2-Substituted Quinazoline-8-acetic Acid Esters, Synthetic Communications,
28:3, 475-483, DOI: 10.1080/00397919808005102
To link to this article: http://dx.doi.org/10.1080/00397919808005102
Published online: 15 Aug 2006.
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Date: 14 June 2016, At: 11:00