## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Studies on pyrrolidinones. Preparation of 1,5,6-10b-tetrahydro-2H-pyrrolo[1,2-c]quinazoline-3-ones from pyroglutamic acid
✍ Scribed by Samira El Ghammarti; Benoít Rigo; Hechmi Mejdi; Jean-Pierre Hénichart; Daniel Couturier
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2000
- Tongue
- English
- Weight
- 475 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Tetrahydro‐2__H__‐pyrrolo[1,2‐c]quinazoline‐3‐ones are easily obtained from the Friedel‐Crafts cyclization of N‐arylaminomethyl pyroglutamic acids. This reaction occurrs via an acyliminium salt formed by decarboxylation of the acid function.
📜 SIMILAR VOLUMES
## Abstract ^1^H and ^13^C spectroscopic data for 5__H__‐[1,3]thiazolo[2,3‐__b__]quinazolin‐5‐one and 12__H__‐[1,3]benzothiazolo[2,3‐__b__]quinazolin‐12‐one derivatives were fully assigned by combination of one‐ and two‐dimensional experiments (DEPT, HMBC and HMQC). Both heterocyclic systems show s
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract On treatment with lead tetraacetate (Pb(OAc)~4~), the 1‐(alkylidene)‐1,2,3,4‐tetrahydro‐__N__‐(trichloroacetyl)isoquinolines **2a**–**2c** as well as the tribromoacetyl derivative **4** undergo an oxidative cyclization with concomitant migration of the trihalogenomethyl group to afford
## Abstract For Abstract see ChemInform Abstract in Full Text.