## 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
Conjugate addition of nitrogen nucleophiles to an α, β-unsaturated pyrrolidinone
✍ Scribed by Philip W.H Chan; Ian F Cottrell; Mark G Moloney
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 236 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The conjugate addition of nitrogen nucleophiles to ct,13-unsaturated lactam lb under very mild conditions occurs in good yield with high diastereoselectivity. Deprotection provides a simple access to 13-aminopyrrolidinones in excellent overall yield.
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## 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
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## Abstract 5,6‐Dihydropyridine‐2‐thiones 2 are synthesized from 5,6‐dihydropyridin‐2‐ones 1 and Lawesson reagent. Stereoselective Michael‐like addition of amines, methylhydrazine or functionalized thiols affords __trans__ piperidine‐2‐thiones 5 with the corresponding heterosubstituent in position