efficient catalytic asymmetric synthesis of trans-5-aryl-2-substituted cyclohexanones by...

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2007 Polyphenyl derivatives Q 0700 Efficient Catalytic Asymmetric Synthesis of trans-5-Aryl-2-substituted Cyclohex- anones by Rhodium-Catalyzed Conjugate Arylation of Racemic 6-Substituted Cyclohexenones. — The reaction affords a nearly 1:1 mixture of trans- and cis-dia- stereomers after the first step. The following epimerization with sodium ethoxide in ethanol leads to the corresponding trans-configurated target compounds. — (CHEN, Q.; SOETA, T.; KURIYAMA, M.; YAMADA, K.-I.; TOMIOKA*, K.; Adv. Synth. Catal. 348 (2006) 18, 2604-2608; Grad. Sch. Pharm. Sci., Kyoto Univ., Sakyo, Kyoto 606, Japan; Eng.) — Y. Steudel 19- 092

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2007

Polyphenyl derivativesQ 0700 Efficient Catalytic Asymmetric Synthesis of trans-5-Aryl-2-substituted Cyclohex-

anones by Rhodium-Catalyzed Conjugate Arylation of Racemic 6-Substituted Cyclohexenones. — The reaction affords a nearly 1:1 mixture of trans- and cis-dia-stereomers after the first step. The following epimerization with sodium ethoxide in ethanol leads to the corresponding trans-configurated target compounds. — (CHEN, Q.; SOETA, T.; KURIYAMA, M.; YAMADA, K.-I.; TOMIOKA*, K.; Adv. Synth. Catal. 348 (2006) 18, 2604-2608; Grad. Sch. Pharm. Sci., Kyoto Univ., Sakyo, Kyoto 606, Japan; Eng.) — Y. Steudel

19- 092