An Efficient Synthesis of Stereodefined Enynes and Dienes via Pd-Catalyzed Reaction of Chloroenynes and Chlorodienes with Grignard Reagents
✍ Scribed by Parfait Ramiandrasoa; Bernard Bréhon; Armelle Thivet; Mouâd Alami*; Gérard Cahiez
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 481 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
In the presenceof PdC12(PPb3)2 and Et3N,cbloroenynesandchlorodienesreact rapidly under mild conditions with various Grignard reagents to give isometricallypure conjugated enynes, dienes, dienynesandtrienes in goodisolatedyields. 01997 Publishedby Elsevier Science Ltd.
📜 SIMILAR VOLUMES
Efficient Synthesis of 1,1-Diaryl 1,2-Dienes via Pd(0)-Catalyzed Coupling of Aryl Halides with Allenic/Propargylic Zinc Reagents. -The title reaction is proposed to involve oxidative addition of halides to Pd(0) to form an organopalladium intermediate. This is trapped by an allenic or propargylic z
## 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 of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v