Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (dicyclohexylphosphine)}nickel(II)
Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (dicyclohexylphosphine)}nickel(II) Basic information
- Product Name:
- Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (dicyclohexylphosphine)}nickel(II)
- Synonyms:
-
- CHLORO(4-CYANOPHENYL){(R)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYL(DICYCLOHEXYLPHOSPHINE)}NICKEL(II)
- )[(R)-1-[(S)-2-(dicycL
- CAS:
- 2049086-35-1
- MF:
- C43H55ClFeNNiP2
- MW:
- 797.86
- Mol File:
- 2049086-35-1.mol
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Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (dicyclohexylphosphine)}nickel(II) Chemical Properties
- form
- solid
- color
- orange
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Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (dicyclohexylphosphine)}nickel(II) Usage And Synthesis
Uses
- Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions.
- Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines.
- Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions.
- Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts.
Uses
Amination of aryl chlorides, bromides and sulfonates with ammonia. Amination of aryl carbamates with ammonia or ammonium salts.
reaction suitability
core: nickel
reaction type: Cross Couplings
reagent type: catalyst
reaction type: Asymmetric synthesis
Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (dicyclohexylphosphine)}nickel(II)Supplier
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Chloro(4-cyanophenyl){(R)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl (dicyclohexylphosphine)}nickel(II)(2049086-35-1)Related Product Information
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