A direct route to angularly substituted hydrindanes. Formal synthesis of bakkenolide-A and synthesis of an advanced intermediate to umbellactal

Tetrahedron

Volumn 65, Issue 45, 2009, Pages 9202-9210

  Maity, Soumitra ^a   Ghosh, Subrata ^a  

^a DEPARTMENT OF MATERIALS SCIENCE   (India)

Author keywords

Hydrindanes; Metathesis; Spiro lactones; Terpenes

Indexed keywords

1 (1,3,3A,4,6A,7,8,9 OCTAHYDROINDENO[3 A,4 C]THIOPHEN 8 YL)ETHANE 1,2 DIOL; 1 (2,3,3A,4,7A HEXAHYDRO 3A,4 DIMETHYL METHANESULFONATE 1H INDEN 2YL)ETHANE 1,2 DIOL; 1 (OCTAHYDRO 3A,4 DIMETHYL 1H INDEN 2 YL) 2 (TERT BUTYL)DIMETHYLSILYLOXY ETHANONE; 1 (OCTAHYDRO 3A,4 DIMETHYL 1H INDEN 2 YL) 2 HYDROXYETHANONE; 1 (OCTAHYDRO 3A,4 DIMETHYL 1H INDEN 2 YL)ETHANE 1,2 DIOL; 1 (OTAHYDRO 3A,4 DIMETHYL 1H INDEN 2 YL)ETHANONE; 2 ETHYL OCTAHYDRO 3A,4 DIMETHYL 1H INDENE; 2,3,3A,4,5,7A HEXAHYDRO 3A,4 BIS(HYDROXYMETHYL) 2 VINYL 1H INDENE; 2,3,3A,4,5,7A HEXAHYDRO 3A,4 BIS(METHYLSULFONYLOXYMETHY) 2 VINYL 1H INDENE; 2,3,3A,4,5,7A HEXAHYDRO 3A,4 DIHYDROXY METHYL 2 VINYL 1H INDENE DERIVATIVE; 2,3,3A,4,5,7A HEXAHYDRO 4 METHYL 2 VINYL 1H INDEN 3A YL)METHYL METHANESULFONATE; 3A,4,6A,7,8,9 HEXAHYDRO 4 (METHOXY METHOXY) 8 VINYLINDENO(3A,4 C]FURAN 3(1H) ONE; 3A,4,6A,7,8,9 HEXAHYDRO 4 (TERT BUTYL)DIMETHYLSILOXY 8 VINYLINDENOL[2A,4 C]FURAN 3(1H) ONE; 3A,4,6A,7,8,9 HEXAHYDRO 4 (TERT BUTYL)DIMETHYLSILYLOXY 8 VINYLINDENOL[3A,4 C]FURAN 3(1H) ONE; 3A,4,6A,7,8,9 HEXAHYDRO 4 HYDROXY 8 VINYL INDENO[3A,4 C]FURAN 3(1H) ONE; 3A,4,6A,7,8,9 HEXAHYDRO 4 HYDROXY 8 VINYLINDENO[3A,4 C]FURAN 3(1H) ONE; 3A,4,6A,7,8,9 HEXAHYDRO 8 VINYLINDENO[3A,4 C]FURAN 3(1H) ONE DERIVATIVE; 3A,4,6A,7,8,9 HEXAHYDROXY 8 VINYLINDENOL[3A,4 C]FURAN 3(1H) ONE; 6A,7,8,9 TETRAHYDRO 8 VINYLINDENO[3A,4 C]FURAN 3(1H) ONE; BAKKANOLIDE A; DIMETHYL 2,3,3A,4,5,7A HEXAHYDRO 2 VINYL 1H INDENE 3ALPHA,4 DICARBOXYLATE DERIVATIVE; DITERPENE; ETHYL 2 (OCTAHYDRO 3A,4 DIMETHYL 1H INDEN 2 YL) 2 OXOETHYL CARBONATE; HYDRINDANE DERIVATIVE; METHYL 2 (1 (METHOXYCARBONY)BUT 3 ENYL)BICYCLO[2.2.1]HEPT 5 ENE 2 CARBOXYLATE; NORBORNENE DERIVATIVE; SPIRONOLACTONE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; COLUMN CHROMATOGRAPHY; DIELS ALDER REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; PRIORITY JOURNAL; STEREOCHEMISTRY;

EID: 70349773097     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.09.029     Document Type: Article

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