Asymmetric Hydrogenation Catalysts (37)

Asymmetric hydrogenation catalysts are employed in asymmetric hydrogenation reactions to selectively produce a specific stereoisomer, such as a chiral isomer, in molecules with varying stereochemistry. These catalysts play a crucial role in organic synthesis, medicinal chemistry, natural product synthesis, and other disciplines, especially in the production of chiral compounds.

(S)-RuCl[(p-cyMene)(SEGPHOS)]Cl;[RuCl(p-cymene)((S)-segphos(regR))]Cl;CHLORO[(S)-(-)-5,5'-BIS(DIPHENYLPHOSPHINO)-4,4'-BI-1,3-BENZODIOXOLE](P-CYMENE)RUTHENIUM(II) CHLORIDE,[RUCL(P-CYMENE)((S)-SEGPHOS;[RUCL(P-CYMENE)((S)-SEGPHOS)]CL;)]Cl;-bi-1,3-benzodioxole](p-cymene)ruthenium(II) chloride,[RuCl(p-cymene)((S)-segphos;Chloro[(S)-(-)-5,5'-bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole](p-cymene)ruthenium(II) chloride [RuCl(p-cymene)((S)-segphos(R))]Cl;[RuCl(p-cymene)((S)-segphos[R])]Cl structure diagram

(S)-RuCl[(p-cyMene)(SEGPHOS)]Cl;[RuCl(p-cymene)((S)-segphos(regR))]Cl;CHLORO[(S)-(-)-5,5'-BIS(DIPHENYLPHOSPHINO)-4,4'-BI-1,3-BENZODIOXOLE](P-CYMENE)RUTHENIUM(II) CHLORIDE,[RUCL(P-CYMENE)((S)-SEGPHOS;[RUCL(P-CYMENE)((S)-SEGPHOS)]CL;)]Cl;-bi-1,3-benzodioxole](p-cymene)ruthenium(II) chloride,[RuCl(p-cymene)((S)-segphos;Chloro[(S)-(-)-5,5'-bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole](p-cymene)ruthenium(II) chloride [RuCl(p-cymene)((S)-segphos(R))]Cl;[RuCl(p-cymene)((S)-segphos[R])]Cl

ACLGWK695

944451-29-0

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Total: 30