The Baylis-Hillman reaction: An expedient synthesis of (Z)-keto allyl bromides and chlorides
✍ Scribed by Deevi Basavaiah; Rachakonda Suguna Hyma; Kisari Padmaja; Marimganti Krishnamacharyulu
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 349 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
A simple and expedient synthesis of (Z)-keto allyl bromides and chlorides, from the Baylis-Hillman adduets is described.
📜 SIMILAR VOLUMES
## 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.
## 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
Treatment of Baylis-Hillman adducts 1 with bromo(dimethyl)sulfonium bromide, Br(Me 2 )S + Br À , in MeCN was found to stereoselectively afford (Z)-and (E)-allyl bromides 2. The reaction is rapid at room temperature, high-yielding, and highly stereoselective.
## 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 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.