Stereodivergent Formation of Alkenylsilanes: syn or anti Hydrosilylation of alkynes catalyzed by a cyclopentadienylcobalt(I) chelate bearing a pendant phosphane tether

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OriginalspracheEnglisch
Seiten (von - bis)833-836
Seitenumfang4
FachzeitschriftAdvanced Synthesis and Catalysis
Jahrgang348
Ausgabenummer7-8
PublikationsstatusVeröffentlicht - 5 Mai 2006

Abstract

The hydrosilylation of alkynes is catalyzed by the di-tert- butylphosphanylethylcyclopentadienyl-cobalt chelate 1. While the reaction of internal alkynes exclusively affords syn hydrosilylation products with triethylsilane, the reaction with triethoxysilane shows predominant anti stereoselectivity. Reactions of terminal alkynes are less selective with triethylsilane and result in cyclotrimerization when triethoxysilane is used.

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Stereodivergent Formation of Alkenylsilanes: syn or anti Hydrosilylation of alkynes catalyzed by a cyclopentadienylcobalt(I) chelate bearing a pendant phosphane tether. / Yong, Li; Kirleis, Karin; Butenschön, Holger.
in: Advanced Synthesis and Catalysis, Jahrgang 348, Nr. 7-8, 05.05.2006, S. 833-836.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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title = "Stereodivergent Formation of Alkenylsilanes: syn or anti Hydrosilylation of alkynes catalyzed by a cyclopentadienylcobalt(I) chelate bearing a pendant phosphane tether",
abstract = "The hydrosilylation of alkynes is catalyzed by the di-tert- butylphosphanylethylcyclopentadienyl-cobalt chelate 1. While the reaction of internal alkynes exclusively affords syn hydrosilylation products with triethylsilane, the reaction with triethoxysilane shows predominant anti stereoselectivity. Reactions of terminal alkynes are less selective with triethylsilane and result in cyclotrimerization when triethoxysilane is used.",
keywords = "Alkynes, Cobalt, Hydrosilylation, P ligands, Triethoxysilane, Triethylsilane",
author = "Li Yong and Karin Kirleis and Holger Butensch{\"o}n",
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month = may,
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journal = "Advanced Synthesis and Catalysis",
issn = "1615-4150",
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TY - JOUR

T1 - Stereodivergent Formation of Alkenylsilanes

T2 - syn or anti Hydrosilylation of alkynes catalyzed by a cyclopentadienylcobalt(I) chelate bearing a pendant phosphane tether

AU - Yong, Li

AU - Kirleis, Karin

AU - Butenschön, Holger

PY - 2006/5/5

Y1 - 2006/5/5

N2 - The hydrosilylation of alkynes is catalyzed by the di-tert- butylphosphanylethylcyclopentadienyl-cobalt chelate 1. While the reaction of internal alkynes exclusively affords syn hydrosilylation products with triethylsilane, the reaction with triethoxysilane shows predominant anti stereoselectivity. Reactions of terminal alkynes are less selective with triethylsilane and result in cyclotrimerization when triethoxysilane is used.

AB - The hydrosilylation of alkynes is catalyzed by the di-tert- butylphosphanylethylcyclopentadienyl-cobalt chelate 1. While the reaction of internal alkynes exclusively affords syn hydrosilylation products with triethylsilane, the reaction with triethoxysilane shows predominant anti stereoselectivity. Reactions of terminal alkynes are less selective with triethylsilane and result in cyclotrimerization when triethoxysilane is used.

KW - Alkynes

KW - Cobalt

KW - Hydrosilylation

KW - P ligands

KW - Triethoxysilane

KW - Triethylsilane

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DO - 10.1002/adsc.200606028

M3 - Article

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VL - 348

SP - 833

EP - 836

JO - Advanced Synthesis and Catalysis

JF - Advanced Synthesis and Catalysis

SN - 1615-4150

IS - 7-8

ER -

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