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ChemInform Abstract: Highly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides Catalyzed by AgOAc/TF-BiphamPhos.

✍ Scribed by Chun-Jiang Wang; Zhi-Yong Xue; Gang Liang; Zhou Lu

Publisher
John Wiley and Sons
Year
2009
Weight
34 KB
Volume
40
Category
Article
ISSN
0931-7597

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✦ Synopsis

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 β€œFull Text” option. The original article is trackable via the β€œReferences” option.

πŸ“œ SIMILAR VOLUMES

Silver Acetate/TF-BiphamPhos-Catalyzed e
Silver Acetate/TF-BiphamPhos-Catalyzed endo-Selective Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Vinyl Phenyl Sulfone
✍ Gang Liang; Min-Chao Tong; Chun-Jiang Wang πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 259 KB πŸ‘ 1 views

The first catalytic endo-selective 1,3-dipolar cycloaddition of azomethine ylides and vinyl phenyl sulfone has been developed successfully. The highly efficient silver acetate (AgOAc)/TF-Bi-phamPhos catalytic system exhibited high reactivity, excellent diastereoselectivity (> 98:2), good enantiosele