The asymmetric Michael-type alkylation of chiral β-enamino esters: Critical role of a benzyl ester group in the racemization of adducts

Tetrahedron Asymmetry

Volumn 16, Issue 23, 2005, Pages 3853-3857

  Pizzonero, Mathieu ^a   Hendra, Frédéric ^b   Delarue Cochin, Sandrine ^a   Tran Huu Dau, Marie Elise ^c   Dumas, Françoise ^a   Cavé, Christian ^a   Nour, Mohammed ^b,d   D'Angelo, Jean ^a  

^a UNIVERSITÉ PARIS SUD   (France)

^b UFR Pharmacie   (France)

^c CNRS   (France)

^d UNIVERSITÉ DE LA NOUVELLE CALÉDONIE   (New Caledonia)

Author keywords

[No Author keywords available]

Indexed keywords

BENZYL DERIVATIVE; CARBON; ESTER DERIVATIVE; METHYL GROUP;

ALKYLATION; ARTICLE; CHIRALITY; MICHAEL ADDITION; PRIORITY JOURNAL; RACEMIZATION;

EID: 28644451287     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2005.10.034     Document Type: Article

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