Stereoselectivity of 1,3-dipolar cycloadditions of L-valine-derived nitrones with methyl acrylate

Tetrahedron

Volumn 59, Issue 18, 2003, Pages 3333-3339

  Blanáriková Hlobilová, Iva ^a   Kubánová, Zuzana ^a   Fišera, Lubor ^a   Cyranski, Michal K ^b   Salanski, Piotr ^c   Jurczak, Janusz ^b,c   Prónayová, Nada ^a  

^a SLOVAK UNIVERSITY OF TECHNOLOGY   (Slovakia)

^b UNIVERSITY OF WARSAW   (Poland)

^c INSTITUTE OF ORGANIC CHEMISTRY   (Poland)

Author keywords

Chiral nitrones; Cycloaddition; High pressure; Isoxazolidines

Indexed keywords

ACRYLIC ACID METHYL ESTER; AMINO ACID DERIVATIVE; BENZYL DERIVATIVE; ESTER DERIVATIVE; ISOXAZOLIDINE DERIVATIVE; NITROGEN; NITRONE DERIVATIVE; OXYGEN; VALINE;

ADDITION REACTION; ARTICLE; ATMOSPHERIC PRESSURE; CHIRALITY; CYCLOADDITION; DEPROTECTION REACTION; DIASTEREOISOMER; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION TIME; SEPARATION TECHNIQUE; STEREOCHEMISTRY; SUBSTITUTION REACTION; TRANS ISOMER;

EID: 0344059122     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)00424-1     Document Type: Article

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