First stereocontrolled reduction of isoxazoline by hydrogenolysis: A new route to iminosugars via cyclic sulfates

Synlett

Volumn , Issue 8, 2002, Pages 1359-1361

  Lemaire, Marielle ^a   Veny, Nicolas ^a   Gefflaut, Thierry ^a   Gallienne, Estelle ^a   Chenevert, Robert ^b   Bolte, Jean ^a  

^a UNIVERSITÉ CLERMONT AUVERGNE   (France)

^b UNIVERSITÉ LAVAL   (Canada)

Author keywords

Cyclic sulfates; Cycloadditions; Glycosidase inhibitors; Iminosugars; Piperidines

Indexed keywords

1 BENZYLOXY 2 NITROETHANE; 1 DEOXYMANNONOJIRIMYCIN; 1 DEOXYNOJIRIMYCIN DERIVATIVE; 2,2 DIMETHYL 4 VINYL 1,3 DIOXOLANE; ETHANE; ISOXAZOLINE DERIVATIVE; PIPERIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CYCLOADDITION; DRUG STRUCTURE; DRUG SYNTHESIS; INHIBITION KINETICS; NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

EID: 0036331047     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2002-32967     Document Type: Article

References (30)