Vinylsulfones as nucleophiles and Michael acceptors in the same step: Stereoselective synthesis of amino acid precursors

Synthesis

Volumn , Issue 19, 2005, Pages 3327-3334

  Díez, David ^a   García, Pilar ^a   Moro, R F ^a   Marcos, Isidro S ^a   Basabe, Pilar ^a   Garrido, Narciso M ^a   Broughton, Howard B ^b   Urones, Julio G ^a  

^a UNIVERSITY OF SALAMANCA   (Spain)

^b ELI LILLY AND COMPANY   (Spain)

Author keywords

Amino acids; Hydride transfer; Molecular model; Stereoselectivity; Synthesis; Transition state; Vinyl sulfones

Indexed keywords

KETONES; NITROGEN COMPOUNDS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

HYDRIDE TRANSFER; MOLECULAR MODEL; STEREOSELECTIVITY; TRANSITION STATE; VINYL SULFONES;

AMINO ACIDS;

AMINO ACID DERIVATIVE; GLYCERALDEHYDE; IMINE; SULFONE DERIVATIVE; VINYL DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; MICHAEL ADDITION; STEREOCHEMISTRY; SYNTHESIS;

EID: 29044437706     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-870005     Document Type: Article

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