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Asymmetric diene cyclization/hydrosilylation/oxidation employing 1-tert-butyl-3,3-dimethyl-1,1-diphenyldisiloxane

✍ 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

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✦ 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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ChemInform Abstract: Asymmetric Diene Cy
✍ Tao Pei; Ross A. Widenhoefer πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons βš– 33 KB

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