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Volumn 64, Issue 42, 2008, Pages 9850-9856

The acyclic dienamine-indoloacrylate addition route to catharanthine

Author keywords

Catharanthine synthesis; Indole alkaloids

Indexed keywords

2 (1,3 DIOXOLAN 2 YL)BUTAN 1 OL; 2 (1,3 DIOXOLAN 2 YL)BUTANAL; BUTYRIC ACID DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; CATHARANTHINE; CIS 4 ETHYL (TOLUENE 4 SULFONYLOXYMETHYL) 2,4A,5,6,7,12 HEXAHYDRO 1H BENZO[2,3]AZEPINO[4,5 B]INDOLE 12B CARBOXYLIC ACID DIMETHYL ESTER; CIS 4 ETHYL 2,4A,5,6,7,12 HEXAHYDRO 1H BENZO[2,3]AZEPINO[4,5 B]INDOLE 2,12B DICARBOXYLIC ACID DIMETHYL ESTER; CIS 5 BENZYL 4 ETHYL (TOLUENE 4 SULFONYLOXYMETHYL) 2,4A,5,6,7,12 HEXAHYDRO 1H BENZO[2,3]AZEPINO[4,5 B]INDOLE 12B CARBOXYLIC ACID DIMETHYL ESTER; CIS 5 BENZYL 4 ETHYL 2 HYDROXYMETHYL 2,4A,5,6,7,12 HEXAHYDRO 1H BENZO[2,3]AZEPINO[4,5 B]INDOLE 12B CARBOXYLIC ACID DIMETHYL ESTER; CIS 5 BENZYL 4 ETHYL 2,4A,5,6,7,12 HEXAHYDRO 1H BENZO[2,3]AZEPINO[4,5 B]INDOLE 2,12B DICARBOXYLIC ACID DIMETHYL ESTER; DIMETHYL 5 BENZYL 4 ETHYL 2,4A,5,6,7,12 HEXAHYDRO 1H BENZO[2,3]AZEPINO[4,5 B]INDOLE 2,12B DICARBOXYLATE; ESTER DERIVATIVE; METHYL 2 (1,3 DIOXOLAN 2 YL)BUTANOATE; METHYL 2 FORMYLBUTYRATE; METHYL 3 BENZYL 1,2,3,4,5,6 HEXAHYDROAZEPINOL[4,5 B]INDOLE 5 CARBOXYLATE; METHYL 4 (1,3 DIOXOLAN 2 YL)HEX 2 ENOATE; METHYL 4 FORMYLHEX 2 HEXENOATE; METHYL 4 FORMYLHEX 3 ENOATE; SODIUM BOROHYDRIDE; TRANS 5 BENZYL 4 ETHYL 2,4A,5,6,7,12 HEXAHYDRO 1H BENZO[2,3]AZEPINO[4,5 B]INDOLE 2,12B DICARBOXYLIC ACID DIMETHYL ESTER; UNCLASSIFIED DRUG;

EID: 50849084470     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.07.044     Document Type: Article
Times cited : (6)

References (27)
  • 16
    • 50849124003 scopus 로고    scopus 로고
    • Unpublished studies at the University of Vermont by Dr. Tiansheng Wang (coauthor in (b)) including aldehyde 6, followed by Dr. Mustapha Soukri with other substituted crotonals;
    • Unpublished studies at the University of Vermont by Dr. Tiansheng Wang (coauthor in (b)) including aldehyde 6, followed by Dr. Mustapha Soukri with other substituted crotonals;
  • 19
    • 2242471423 scopus 로고
    • Prepared by an alternative synthesis in considerably lower yield by: with other cited references
    • Prepared by an alternative synthesis in considerably lower yield by:. Reddy C.P., and Tanimoto S. Synthesis (1987) 575 with other cited references
    • (1987) Synthesis , pp. 575
    • Reddy, C.P.1    Tanimoto, S.2
  • 22
    • 50849135776 scopus 로고    scopus 로고
    • http://www.cambridgesoft.com/ChemDraw.
    • http://www.cambridgesoft.com/ChemDraw.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.