首页> 外文期刊>Russian Chemical Bulletin >Tetraaryl-1,3-dioxolane-4,5-dimethanols as catalysts for the addition of trimethylsilyl cyanide to benzaldehyde and the oxirane ring
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Tetraaryl-1,3-dioxolane-4,5-dimethanols as catalysts for the addition of trimethylsilyl cyanide to benzaldehyde and the oxirane ring

机译:四芳基-1,3-二氧戊环-4,5-二甲醇用作将三甲基甲硅烷基氰化物加至苯甲醛和环氧乙烷环的催化剂

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摘要

The synthesis of 1,2-, 1,3-, and 1,4-phenylene-bis[(4R,5R)-4,5-di(hydroxydiphenylmethyl)-1,3-dioxolane]s (ortho-, meta-, and para-bis-(R,R)-TADDOLs) and bls[4-{[(4R,5R)-4,5-di(hydroxydiphenylmethyl)]-1,3-dioxolan-2-yl}phenyl]methane was carried out. The possibilities of the use of these compounds as catalysts for the C—C bond formation in the addition of Me3SiCN to benzaldehyde and the oxirane ring opening in cyclohexene oxide by Me3SiCN were investigated. The catalytic activity of different bis-(R,R)-TADDOLs in this series depends on their structure.
机译:1,2-,1,3-和1,4-亚苯基-双[(4R,5R)-4,5-二(羟基二苯甲基)-1,3-二氧戊环] s(邻-,间-以及对双-((R,R)-TADDOLs)和bls [4-{[(4R,5R)-4,5-di(hydroxydiphenylmethyl)]-1,3-dioxolan-2-yl} phenyl]甲烷进行了。研究了在Me3SiCN加入苯甲醛中和Me3SiCN在环己烯氧化物中的环氧乙烷开环中,将这些化合物用作形成C-C键的催化剂的可能性。该系列中不同的双-(R,R)-TADDOL的催化活性取决于其结构。

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