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2003 Alcohols Alcohols Q 0230 Preparation of δ-Fluorinated Homoallylic Alcohol Derivatives via Regioselective Hydride Reduction of Allylic Alcohol Derivatives. — It is noteworthy that the reaction of (VIa) with iBu 2 AlH in ether only results in the reduction of the ester moiety. Some more experiments are performed for understanding the mechanism of the reaction. — (NAKAMURA, Y.; OKADA, M.; HORIKAWA, H.; TAGUCHI*, T.; J. Fluorine Chem. 117 (2002) 2, 143-148; Sch. Pharm., Univ. Pharm. Life Sci., Hachioji, Tokyo 192, Japan; Eng.) — K. Schneider 13- 080

Preparation of δ-Fluorinated Homoallylic Alcohol Derivatives via Regioselective Hydride Reduction of Allylic Alcohol Derivatives

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2003 Alcohols

AlcoholsQ 0230 Preparation of δ-Fluorinated Homoallylic Alcohol Derivatives via Regioselective

Hydride Reduction of Allylic Alcohol Derivatives. — It is noteworthy that thereaction of (VIa) with iBu2AlH in ether only results in the reduction of the ester moiety. Some more experiments are performed for understanding the mechanism of the reaction. — (NAKAMURA, Y.; OKADA, M.; HORIKAWA, H.; TAGUCHI*, T.; J. Fluorine Chem. 117 (2002) 2, 143-148; Sch. Pharm., Univ. Pharm. Life Sci., Hachioji, Tokyo 192, Japan; Eng.) — K. Schneider

13- 080