Journal of the American Chemical Society

Catalytic asymmetric synthesis of optically active 2-alkanols via hydrosilylation of 1-alkenes with a chiral monophosphine-palladium catalyst

Y Uozumi, T Hayashi

Index: Uozumi, Yasuhiro; Hayashi, Tamio Journal of the American Chemical Society, 1991 , vol. 113, # 26 p. 9887 - 9888

Full Text: HTML

Citation Number: 282

Abstract

Catalytic asymmetric functionalization of simple prochiral olefis is an important goal in synthetic organic chemistry.'q2 We report here the first successful conversion of alkyl- substituted terminal olefins into optically active secondary alcohols (> 94% ee), 3 which is realized by palladium-catalyzed asymmetric hydrosilylation in the presence of a new chiral monodentate phosphine ligand (MOP, 1) followed by oxidation of the carbonsilicon bond4 ...

Related Articles:

Novel phosphonium chloride-catalyzed dehydrohalogenative Si-C coupling reaction of alkyl halides with trichlorosilane

[Yeon Seok Cho; Kang; Joon Soo Han; Bok Ryul Yoo; Il Nam Jung Journal of the American Chemical Society, 2001 , vol. 123, # 23 p. 5584 - 5585]

Asymmetric Hydrosilylation of 1-Alkenes Catalyzed by Palladium-MOP.

[Uozumi, Yasuhiro; Kitayama, Kenji; Hayashi, Tamio; Yanagi, Kazunori; Fukuyo, Emiko Bulletin of the Chemical Society of Japan, 1995 , vol. 68, # 3 p. 713 - 722]

Organosilicon Compounds. I. Synthesis of Some Long-Chain Tetraalkylsilanes1

[Rosenberg,H. et al. Journal of Organic Chemistry, 1960 , vol. 25, p. 243 - 246]

More Articles...