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Volumn 10, Issue 24, 1999, Pages 4729-4743

Versatile synthesis of P-chiral (ephedrine) AMPP ligands via their borane complexes. Structural consequences in Rh-catalyzed hydrogenation of methyl α-acetamidocinnamate

Author keywords

[No Author keywords available]

Indexed keywords

AMINOPHOSPHINE PHOSPHINITE; BORANE DERIVATIVE; CINNAMIC ACID DERIVATIVE; EPHEDRINE; METHYL ALPHA ACETAMIDOCINNAMIC ACID; ORGANOLITHIUM COMPOUND; PHENYLALANINE DERIVATIVE; PHOSPHINE DERIVATIVE; RHODIUM; UNCLASSIFIED DRUG;

EID: 0033397829     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(99)00510-8     Document Type: Article
Times cited : (52)

References (54)
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    • HC1 acidolysis of aminophosphines 2a (or 2b), leads to chlorophosphine boranes 3a (or 3b) with inversion of configuration: (a) Ref. 7f. (b) Moulin, D. PhD thesis, 1999, Cergy-Pontoise.
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    • note
    • Asymmetric hydrogenation of subtrate 6 using (+)-PPHOS 5a′-Rh complex in benzene, have been reported to give the aminoester 7 in 82% e.e. by Pracejus and colleagues (Ref. 3b).


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