![]() (1R,2R)-1-(DIPHENYLPHOSPHINO)-1-PHENYLPROPAN-2-AMINE structure
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Common Name | (1R,2R)-1-(DIPHENYLPHOSPHINO)-1-PHENYLPROPAN-2-AMINE | ||
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CAS Number | 799297-44-2 | Molecular Weight | 319.38000 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C21H22NP | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | N/A | |
Symbol |
![]() GHS05 |
Signal Word | Danger |
Chemoselective hydrogenation of imides catalyzed by Cp*Ru(PN) complexes and its application to the asymmetric synthesis of paroxetine.
J. Am. Chem. Soc. 129 , 290, (2007)
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Hydrogenation of N-acylcarbamates and N-acylsulfonamides catalyzed by a bifunctional [Cp*Ru(PN)] complex.
Angew. Chem. Int. Ed. Engl. 48 , 1324, (2009) Awakening of the Cp one: The bifunctional complex 1 facilitates the interaction with substrates bearing less electrophilic carbon atoms than ketones, epoxides, and imides. The title reaction was applicable to the reduction of Evans' asymmetric alkylation prod... |
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D. Amoroso, T.W. Graham et al.
Aldrichimica Acta 41 , 1, 15, (2008)
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T. Hayashi, M. Konishi et al.
J. Org. Chem. 48 , 2195, (1983)
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DELETEile chiral bidentate ligands derived from alpha-amino acids: synthetic applications and mechanistic considerations in the palladium-mediated asymmetric allylic substitutions.
J. Org. Chem. 65 , 4227, (2000) A new class of chiral amidine-phosphine hybrid ligands 7a,b, which are readily accessible from the corresponding alpha-amino acids, were developed. A versatility for construction of new ligands is desirable, by which a variety of reactions and substrates beco... |
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Highly practical and enantioselective cu-catalyzed conjugate addition of alkylzinc reagents to cyclic enones at ambient temperature.
Org. Lett. 5 , 3201, (2003) [reaction: see text] A new ligand for Cu-catalyzed enantioselective additions of dialkylzincs to cyclic enones has been developed. In addition to providing good to excellent enantioselectivities with a range of cyclic enones and dialkylzincs, the ligand has s... |
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