𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of the 2H-Quinolizin-2-one Scaffold via a Stepwise Acylation—Intramolecular Annulation Strategy.

✍ Scribed by Swaminathan R. Natarajan; et al. et al.


Publisher
John Wiley and Sons
Year
2006
Weight
24 KB
Volume
37
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.


📜 SIMILAR VOLUMES


A novel and facile carbodiimide-mediated
✍ Takao Saito; Kensaku Tsuda 📂 Article 📅 1996 🏛 Elsevier Science 🌐 French ⚖ 135 KB

A novel and efficient carbodiimide-mediated synthetic method for new 2,3-dihydro-6Hpyrimido[2,l-b]quinazolin-4(lH)-ones ( 4) is described which involves initial intramolecular addition of an amino-nucleophile to the carbodiimide-cumulenic system, followed by intramolecular hereto conjugate addition

Synthesis of new 2,4-diamino-7H-pyrrolo[
✍ Andre Rosowsky; Hongning Fu; Sherry F. Queener 📂 Article 📅 2001 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 56 KB

## Abstract Selected examples 2,4‐diamino‐7__H__‐pyrrolo[2,3‐__d__]pyrimidines with a phenyl or benzyl group at the 5‐position were synthesized as inhibitors of dihydrofolate reductase (DHFR) from __Pneumocystis carinü__ and __Toxoplasma gondii__, two potentially life‐threatening opportunistic path