Reversal of stereochemistry in a two-step Staudinger reaction by changing the backbone protecting group. Synthesis of NH-trans-3-benzoyloxy-4-aryl-azetidinones

Tetrahedron Letters

Volumn 40, Issue 48, 1999, Pages 8495-8498

  Panunzio, Mauro ^a   Bacchi, Sergio ^a   Campana, Eileen ^a   Fiume, Laura ^a   Vicennati, Paola ^a  

^a CNR   (Italy)

Author keywords

Azetidinones; N silyl imides; Staudinger reaction; Stereocontrol

Indexed keywords

AZETIDINONE DERIVATIVE; FUNCTIONAL GROUP; GLYOXYLIC ACID DERIVATIVE; KETENE DERIVATIVE; SILANE DERIVATIVE;

ARTICLE; CHEMICAL MODIFICATION; DIASTEREOISOMER; STEREOCHEMISTRY; SYNTHESIS;

EID: 0033607741     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01800-6     Document Type: Article

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