Stereoselective reduction of α-hydroxy ketones

作者: Tadashi Nakata , Tadasu Tanaka , Takeshi Oishi

DOI: 10.1016/S0040-4039(00)87969-1

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摘要: Reduction of α-hydroxy ketones with zinc horohydride afforded the erythro -glycols in high stereoselectivity, while reduction of their α-(t-butyldiphenylsily)oxy derivatives with sodium bis(…

参考文章(9)
Takashi Tokuyama, Katsuhiko Shimada, Motokazu Uemura, John W. Daly, The structure of the side chain of the frog alkaloid pumiliotoxin B Tetrahedron Letters. ,vol. 23, pp. 2121- 2124 ,(1982) , 10.1016/S0040-4039(00)87277-9
Gilbert Stork, Ian Paterson, Ferdinand K. C. Lee, Stereoselective synthesis of the chiral sequence of erythronolide A Journal of the American Chemical Society. ,vol. 104, pp. 4686- 4688 ,(1982) , 10.1021/JA00381A035
John A. Katzenellenbogen, Stephen B. Bowlus, Stereoselectivity in the reduction of aliphatic .alpha.-ketols with aluminum hydride reagents Journal of Organic Chemistry. ,vol. 38, pp. 627- 632 ,(1973) , 10.1021/JO00944A001
Stephen B. Bowlus, John A. Katzenellenbogen, Aluminum hydride reduction of .alpha.-ketols. II. Additional evidence for conformational flexibility in the transition state Journal of Organic Chemistry. ,vol. 39, pp. 3309- 3314 ,(1974) , 10.1021/JO00937A001
NguyÊn Trong Anh, Regio- and stereo-selectivities in some nucleophilic reactions ChemInform. ,vol. 11, pp. 145- 162 ,(1980) , 10.1007/BFB0048506