Synthesis of casuarine-related derivatives via 1,3-dipolar cycloaddition between a cyclic nitrone and an unsaturated γ-lactone

Carbohydrate Research

Volumn 344, Issue 2, 2009, Pages 167-176

  Stecko, Sebastian ^a   Solecka, Jolanta ^b   Chmielewski, Marek ^a  

^a INSTITUTE OF ORGANIC CHEMISTRY   (Poland)

^b NATIONAL INSTITUTE OF HYGIENE   (Poland)

Author keywords

1,3 Dipolar cycloaddition; Iminosugars; Necine bases; Nitrone; Pyrrolizidine

Indexed keywords

1,3-DIPOLAR CYCLOADDITION; IMINOSUGARS; NECINE BASES; NITRONE; PYRROLIZIDINE;

HYDROCARBONS; METHANOL;

CYCLOADDITION;

1,2,7 TRIBENZOYLOXY 8 (BENZOYLOXYMETHYL)INDOLIZIDINE; 2 (TERT BUTYLDIPHENYLSILYLOXY) 1 (4,5 DI TERT BUTOXY 3 (TERT BUTYLDIPHENYLSILYLOXYMETHYL) HEXAHYDROPYRROLO[1,2 B]ISOXAZOL 2 YL)ETHANOL; 2 (TERT BUTYLDIPHENYLSILYLOXY) 1 4,5 DI TERT BUTOXY 3 (TERT-BUTYLDIPHENYLSILYLOXYMETHYL)HEXAHYDROPYRROLO[1,2 B]ISOXAZOL 2 YL)ETHYL MESYLATE; 2 ACETOXY 1,3 BIS(ACETOXYMETHYL) 6,7 DI TERT BUTOXY PYRROLIZIDINE; 2 ACETOXY 6,7 DI TERT BUTOXY 3 (ACETOXYMETHYL) 1 METHYL PYRROLIZIDINE; 2 BENZYLOXY 6,7 DI TERT BUTOXY 3 (TERT 2 BENZYLOXY 6,7 DI TERT BUTOXY 3 (TERT BUTYLDIPHENYLSILYLOXYMETHYL)PYRROLIZIDINE; 2,6,7 HYDROXY 1,3 BIS(HYDROXYMETHYL)PYRROLIZIDINE; 2,6,7 TRIACETOXY 1,3 BIS(ACETOXYMETHYL)PYRROLIZIDINE; 2,6,7 TRIACETOXY 3 (ACETOXYMETHYL) 1 METHYL PYRROLIZIDINE; 2,6,7 TRIHYDROXY 3 (HYDROXYMETHYL) 1 METHYL PYRROLIZIDINE; 3 EPI 1 HOMOCASUARINE; 4,5 DI TERT BUTOXY 3 (HYDROXYMETHYL) HEXAHYDROPYRROLO[1,2 B]ISOXAZOL 2 YL)ETHANOL; 5 HYDROXYMETHYL 2(5H)FURANONE; 6,7 DI TERT BUTOXY 1,3 BIS(TERTBUTYLDIPHENYLSILYLOXYMETHYL) 2 HYDROXYPYRROLIZIDINE; 6,7 DI TERT BUTOXY 2 (TERT 6,7 DI TERT BUTOXY 2 (TERTBUTYLDIPHENYLSILYLOXY) 3 (TERT BUTYLDIPHENYLSILYLOXYMETHYL) 1 (PIVALOYLOXMETHYL)PYRROLIZIDINE; 6,7 DI TERT BUTOXY 2 (TERT TERTBUTYLDIPHENYLSILYLOXY) 3 (TERT BUTYLDIPHENYLSILYLOXYMETHYL) 1 HYDROXYMETHYL PYRROLIZIDINE; 6,7 DI TERT BUTOXY 2 (TERT TERTBUTYLDIPHENYLSILYLOXY) 3 (TERT BUTYLDIPHENYLSILYLOXYMETHYL) 1 MESYLOXYMETHYL PYRROLIZIDINE; 6,7 DI TERT BUTOXY 3 (MESYLOXYMETHYL) 2 (PIVALOYLOXY) 1 (PIVALOYLOXYMETHYL)PYRROLIZIDINE; 6,7 DI TERT BUTOXY 3 (TERT BUTYLDIPHENYLSILYLOXYMETHYL) 2 (PIVALOYLOXY) 1 (PIVALOYLOXYMETHYL)PYRROLIZIDINE; 6,7 DI-TERT BUTOXY 3 (TERTBUTYLDIPHENYLSILYLOXYMETHYL) 2 HYDROXY 1 (PIVALOYLOXYMETHYL)PYRROLIZIDINE; 7,8 DI TERT BUTOXY 2 (MESYLOXYMETHYL) 3,3 DIMETHYLOCTAHYDRO[1,3]DIOXEPINO[5,6 D]PYRROLO[1,2 B]ISOXAZOLE; 7,8 DI TERT BUTOXY 2 (TERT BUTYLDIPHENYLSILYLOXYMETHYL) [1,3]DIOXEPINO[5,6 D]PYRROLO[1,2 B]ISOXAZOLE; 7,8-DI TERT BUTOXY 2,3,3 TRIMETHYLOOCTAHYDRO[1,3]DIOXEPINO[5,6 D]PYRROLO[1,2 B]ISOXAZOLE; FURANONE DERIVATIVE; GAMMA LACTONE DERIVATIVE; NITROGEN; NITRONE; OXYGEN; PYRROLIZIDINE ALKALOID; TARTARIC ACID; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CHEMICAL STRUCTURE; CYCLOADDITION; HYDROGENOLYSIS; PRIORITY JOURNAL; REDUCTION; SYNTHESIS;

ALKALOIDS; LACTONES; MOLECULAR STRUCTURE; NITROGEN OXIDES; PYRROLES; PYRROLIZIDINE ALKALOIDS;

EID: 57749197179     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2008.10.016     Document Type: Article

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