| Identification | Back Directory | [Name]
(R)-2-[(R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]-4-ISOPROPYL-2-OXAZOLINE TRIPHENYLPHOSPHINE RUTHENIUM(II) CHLORIDE COMPLEX | [CAS]
849921-25-1 | [Synonyms]
NAUD CATALYST SK-N003-1Z
(+)-DICHLORO[(4R)-4-(I-PROPYL)-2-{(R)-2-(DIPHENYLP
(R)-2-[(R)-2-(Diphenylphosphino)ferrocenyl]-4-isopropyl-2-oxazoline triphenylpho
(R)-4-Isopropyl-2-[(R)-2-(diphenylphosphino)-ferrocen-1-yl]oxazoline triphenylphosphino Ru(Ⅱ) dichloride
(R)-4-Isopropyl-2-[(R)-2-(diphenylphosphino)-ferrocen-1-yl]oxazoline triphenylphosphino Ru(II) dichloride
(+)-Dichloro[(4R)-4-(i-propyl)-2-{(R)-2-(diphenylphosphino)ferrocenyl}oxazoline](triphenylphosphine)ruthenium(II)
(+)-DICHLORO[(4R)-4-(I-PROPYL)-2-[(R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]OXAZOLINE](TRIPHENYLPHOSPHINE)RUTHENIUM (II)
(+)-Dichloro[(4R)-4-(iso-propyl)-2-[(R)-2-(diphenylphosphino)ferrocenyl]oxazoline](triphenylphosphine)ruthenium(II)
(R)-2-[(R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]-4-ISOPROPYL-2-OXAZOLINE TRIPHENYLPHOSPHINE RUTHENIUM(II) CHLORIDE COMPLEX
(S)-1-(DIPHENYLPHOSPHINO)-2-[(R)-4-ISOPROPYL-2-OXAZOLIN-2-YL]FERROCENE TRIPHENYLPHOSPHINE RUTHENIUM(II) CHLORIDE COMPLEX
(+)-Dichloro[(4R)-4-(i-propyl)-2-{(R)-2-(diphenylphosphino)ferrocenyl}oxazoline]
(triphenylphosphine)ruthenium (II)
(R)-2-[(RP)-2-(Diphenylphosphino)ferrocenyl]-4-isopropyl-2-oxazoline triphenylphosphine ruthenium(II) chloride Complex
(s)-1-(diphenylphosphino)-2-[(r)-4-isopropyl-2-oxazolin-2-yl]ferrocene triphenylphosphine ruthenium(ii) chloride complex (acc to cas)
Naud Catalyst SK-N003-1z, (1S)-1-(Diphenylphosphino)-2-[(R)-4-isopropyl-2-oxazolin-2-yl]ferrocene Triphenylphosphine Ruthenium(II) chloride Complex (acc to CAS) | [Molecular Formula]
C46H43Cl2FeNOP2Ru 10* | [MDL Number]
MFCD08459356 | [MOL File]
849921-25-1.mol | [Molecular Weight]
915.61 |
| Questions And Answer | Back Directory | [Uses]
(+)-Dichloro[(4R)-4-(i-propyl)-2-{(R)-2-(diphenylphosphino)ferrocenyl}oxazoline](triphenylphosphine)rutheniuM(II) can be used as catalyst used for the oxidative kinetic resolution of racemic alcohols, the extremely high enantioselective transfer hydrogenation of ketones and the oxidative kinetic resolution of alcohols and the asymmetric hydrosilylation of ketones and imine.
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