Studies on pyrrolidinones. Synthesis of some bioisosteres of 3,3,5-trimethylcyclohexyl pyroglutamate
✍ Scribed by Benoǐt Rigo; Claude Laruelle
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 332 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
The synthesis of new N‐(4‐chlorobenzyl) and N‐(4‐chlorobenzoyl)pyroglutamic esters and amids whose the structure conserves the main structural features of the cholesterol lowering agent crilvastatin is described.
📜 SIMILAR VOLUMES
## Abstract The synthesis of esters, amides, pyrrolidinone and succinimide analogs of a new inhibitor of tubulin polymerization, methyl __N__‐(3,4,4′,5‐tetramethoxybenzhydryl)pyroglutamate (HEI 81) was studied.
## 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
## 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
## Abstract Some ways to use the __N__‐acyl iminium salt methodologies to synthesize a new inhibitor of tubulin polymerization, methyl __N__‐(3,4,4′,5‐tetramethoxybenzhydryl)pyroglutamate (HEI 81) were studied. The most interesting reactions utilize a new pyroglutamic lactone (3‐(3,4,5‐trimethoxyph