A combined RCM-Bischler-Napieralski strategy towards the synthesis of the carbon skeleton of excentricine and related stephaoxocanes

Tetrahedron

Volumn 64, Issue 42, 2008, Pages 9921-9927

  Larghi, Enrique L ^a   Kaufman, Teodoro S ^a  

^a Universidad Nacional de Rosario   (Argentina)

Author keywords

Bischler Napieralski; Excentricine analogue; Macrolactam cyclization; RCM; Stephaoxocanes

Indexed keywords

1 (5,6 DIMETHOXY 2,3,7,8,9,10,11,12,13,13A DECA HYDROCYCLODECA[IF]ISOQUINOLIN 1 YL)ETHANONE; 1 (8 ALLYL 1 HEX 5 ENYL 6,7 DIMETHOXY 3,4 DIHYDRO 1H ISOQUINOLIN 2 YL) ETHANONE; 1 ALLYL 2,3 DIMETHOXY 5 (2 NITROVINYL)BENZENE; 14,15 DIMETHOXY 4 AZABICYCLO[11.3.1]HEPTADECA 1(16),13(17),14 TRIEN 5 ONE; 3 ALLYL 4,5 DIMETHOXY BENZALDEHYDE; 3,4 DIHYDRO ISOQUINOLINE DERIVATIVE; 3,4 DIHYDROISOQUINOLINE; 5,6 DIMETHOXY 2,3,7,8,9,10,11,12,13,13A DECALHYDRO 1H CYCLODECAL[IF]ISOQUINOLINE; ACETAMIDE; ALKALOID DERIVATIVE; CARBON; CYCLODECA[IJ]ISOQUINOLINE DERIVATIVE; ELETEFINE; EXCENTRICINE; HEPT 6 ENOIC ACID [2 (3 ALLYL 4,5 DIMETHOXY PHENYL) ETHYL]AMIDE; ISOQUINOLINE ALKALOID; N METHYLEXCENTRICINE; NITROGEN; STEPHALONGANINE A; STEPHALONGANINE B; STEPHALONGANINE C; STEPHAOXOCANE DERIVATIVE; STEPHAOXOCANIDINE DERIVATIVE; STEPHAOXOCANINE DERIVATIVE; UNCLASSIFIED DRUG;

ALLYLATION; ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; PRIORITY JOURNAL; RING CLOSING METATHESIS; STEREOCHEMISTRY;

EID: 50549101165     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.08.005     Document Type: Article

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