cas 76333-53-4, R(+)-CATHINONE HYDROCHLORIDE

Articles about 76333-53-4Total 4 be found

Rearrangement of N-tert-butanesulfinyl α-halo imines with alkoxides to N-tert-butanesulfinyl 2-amino acetals as precursors of N-protected and N-unprotected α-amino carbonyl compounds
Reaction of N-tert-butanesulfinyl α-halo imines with alkoxides afforded new N-tert-butanesulfinyl 2-amino acetals in good to excellent yield. These N-tert-butanesulfinyl 2-amino acetals are convenient precursors for the TMSOTf-promoted synthesis of the co
Colpaert, Filip,Mangelinckx, Sven,Denolf, Bram,De Kimpe, Norbert
experimental part
p. 6023 - 6032
(2012/10/08)

An efficient synthesis of both enantiomers of Cathinone by regioselective reductive ring opening of substituted aziridines
Both enantiomers of Cathinone were prepared as HCl salts from N-(R)-α-methylbenzylaziridine-2(S)-carboxaldehyde 2c and its enantiomer N-(S)-α-methyl-benzylaziridine-2(R)-carboxaldehyde 3c in high yield. This process makes it possible to prepare other aromatic and heteroaromatic analogs of Cathinone efficiently.
Hwang, Gweon Il,Chung, Jae-Ho,Lee, Won Koo
p. 12111 - 12116
(2007/10/03)

Enantioselective synthesis of both enantiomers of cathinone via the microbiological reduction of 2-azido-1-phenyl-1-propanone
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Besse,Veschambre,Dickman,Chenevert
p. 8288 - 8291
(2007/10/02)