(S)-(+)-1-[(R)-2-(Diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine ethanol adduct, min. 97% (S)-(R)-JOSIPHOS,(S)-1 - [(R)-2 - (二苯基膦)二茂铁基]乙基二环己基膦乙醇加合物 , min. 97%
(S)-1 - [(R)-2 - (二苯基膦)二茂铁基]乙基二环己基膦乙醇加合物 , min. 97%
(S)-(+)-1-[(R)-2-(Diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine ethanol adduct, min. 97% (S)-(R)-JOSIPHOS
品牌: Strem
产品编号: 26-1211
分子式: C??H??FeP?·CH?CH?OH
分子量: 594.59 (640.66)
纯度: min. 97%
包装库存价格
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基本信息

安全信息

存储条件Store at 2-8℃

化学和物理性质

产品描述

Technical Notes:

1. Ligands of this type are currently used industrially in the stereoselective synthesis of commercial products 1,2. These ferrocene based phosphine ligands have wide application in the stereoselective hydrogenation of substituted acetamidoacrylates, enol acetates, ß-ketoesters and simple alkenes

2. Pd-catalyzed, enantioselective, intramolecular a-substituted cyclic ketones: facile synthesis of functionalized chiral spirobicycles.

3.Asymmetric boron conjugate addition of a,ß-unsaturated carbonyl compounds catalyzed by CuOTf/Josiphos under non-alkaline conditions

4.Chiral amides via copper cata lyzed enantioselective conjugate additicon 5. Ruthenium-catalyzed enantioselective synthesis of ß-amino alcohols from 1,2-diols by "borrowing hydrogen". 6.Cobalt catalyzed asymmetric addition of silylacetylenes to 1, 1-disubstituted allenes. 7.L igand for Catalytic Asymmetric Synthesis of Phosphine Boronates . 8. Ligand for Enantioselective Synthesis of Allylboronates and Allylic Alcohols by Cu-Catalyzed 1 ,6-Boration.

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