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(R,R)-(-)-N,N-双(3,5-二叔丁亚水杨基)-1,2-环己烷 135616-40-9

(R,R)-(-)-N,N-双(3,5-二叔丁亚水杨基)-1,2-环己烷 (R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINE 135616-40-9

(R,R)-(-)-N,N-双(3,5-二叔丁亚水杨基)-1,2-环己烷 (R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINE 135616-40-9

(R,R)-(-)-N,N-双(3,5-二叔丁亚水杨基)-1,2-环己烷
(R,R)-(-)-N,N-双(3,5-二叔丁亚水杨基)-1,2-环己烷;(R,R)-N,N-双(3,5-二叔丁基水杨醛基)-1,2-环己二胺;(R,R)-(-)-N,N'-双(3,5-二叔丁基邻羟亚苄基)-1,2-环己二胺;(R,R)-(-)-N,N'-双(3,5-二叔丁基亚水杨基)-1,2-环己烷二胺;(1R,2R)-N,N'-双(3,5-二叔丁亚水杨基)-1,2-环己烷;R)-雅可布逊配体;(R,R)-JACOBSEN配体1G;(R,R)-雅可布逊配体
(R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINE
(RR)-(-)-NN''-BIS(35-DI-T-BU-SALICYL.)-12-CYCLOHEXANEDIA96+%;N,N'-bis(3,5-dibutylsalicylidene)-1,2-cyclohexanediamine;(1R,2R)-(-)-1,2-Cyclohexanediamino-N,N'-bis(3,5-di-t-butylsalicylidene),98%(R,R)-JacobsenLigand;1R,2R-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaMine;2-((E)-((1R,2R)-2-((E)-3,5-di-tert-butyl-2-hydroxybenzylideneaMino)cyclohexyliMino)Methyl)-4,6-di-tert-butylphenol;)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaMine;(R,R)-(-)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine,98%;(R,R)-(-)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine(R,R)-JacobsenLigand
135616-40-9
C36H54N2O2
546.84
1.0110 (rough estimate)
205-207 °C(lit.)
619.74°C (rough estimate)
1.5300 (estimate)
Chloroform (Slightly), Dichloromethane (Slightly)
Inert atmosphere,Room Temperature

制备 (R,R)-(-)-N,N-双(3,5-二叔丁亚水杨基)-1,2-环己烷可由(R,R)-1,2-环己二胺L-酒石酸盐与3,5-二叔丁基-2-羟基苯甲醛一步制备得到。

用途 配体,参与非对称催化反应。用于制备Jacobsen催化剂,应用于缺失功能基团烯烃的对映选择性环氧化反应。(R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine


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