Enantioselective access to all-trans 5-alkylpiperidine-3,4-diols: Application to the asymmetric synthesis of the 1-n-iminosugar (+)-isofagomine

Synthesis

Volumn , Issue 19, 2009, Pages 3251-3258

  Rives, Arnaud ^a   Génisson, Yves ^a   Faugeroux, Vanessa ^a   Saffon, Nathalie ^b   Baltas, Michel ^a  

^a UPS)   (France)

^b UNIVERSITÉ PAUL SABATIER   (France)

Author keywords

Epoxide opening; Iminosugar; Piperidine; Ring enlargement

Indexed keywords

ASYMMETRIC SYNTHESIS; ENANTIOSELECTIVE; EPOXIDE OPENING; IMINOSUGAR; IMINOSUGARS; ISOFAGOMINE; OXIRANES; PIPERIDINE; RING ENLARGEMENT; RING ENLARGEMENT REACTIONS; STEREO-SELECTIVE;

CYANIDES; ELECTRON TRANSITIONS;

SYNTHESIS (CHEMICAL);

CYANIDE; EPOXIDE; ETHYLENE OXIDE; FAGOMINE; IMINOSUGAR; PIPERIDINE DERIVATIVE;

ARTICLE; ASYMMETRIC SYNTHESIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; ENANTIOSELECTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; INFRARED SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; X RAY DIFFRACTION;

EID: 70449371824     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0029-1216935     Document Type: Article

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