## 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 βFull Textβ option. The original article is trackable v
β¦ LIBER β¦
Asymmetric diene cyclization/hydrosilylation/oxidation employing 1-tert-butyl-3,3-dimethyl-1,1-diphenyldisiloxane
β Scribed by Tao Pei; Ross A Widenhoefer
- Book ID
- 104210873
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 83 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
A 1:1 mixture of (N N)Pd(Me)Cl [N N=(R)-(+)-4-isopropyl-2-(2-pyridinyl)-2-oxazoline] (1) and NaBAr 4 [Ar=3,5-C 6 H 3 (CF 3 ) 2 ] catalyzed the asymmetric cyclization/hydrosilylation of functionalized 1,6-dienes with 1-tert-butyl-3,3-dimethyl-1,1-diphenyldisiloxane at -20Β°C to form silylated cyclopentanes in good yield with up to 95% ee. These silylated carbocycles underwent oxidative cleavage of the C Si bond with H 2 O 2 at room temperature to form the corresponding alcohols.
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