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Volumn 9, Issue 26, 2007, Pages 5561-5564

Remarkable effect of N-substituent on enantioselective ruthenium-catalyzed propargylation of indoles with propargylic alcohols

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNE; INDOLE DERIVATIVE; PROPANOL; PROPARGYL ALCOHOL; RUTHENIUM; UNCLASSIFIED DRUG;

EID: 38349176541     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol7025203     Document Type: Article
Times cited : (111)

References (31)
  • 1
    • 0002527986 scopus 로고    scopus 로고
    • For recent reviews, see: a
    • For recent reviews, see: (a) Tokuyama, H.; Fukuyama, T. Chem. Rec. 2002, 2, 37.
    • (2002) Chem. Rec , vol.2 , pp. 37
    • Tokuyama, H.1    Fukuyama, T.2
  • 5
    • 34249936878 scopus 로고    scopus 로고
    • For a recent example, see
    • For a recent example, see: Stuart, D. R.; Fagnou, K. Science 2007, 316, 1172.
    • (2007) Science , vol.316 , pp. 1172
    • Stuart, D.R.1    Fagnou, K.2
  • 6
    • 0037680718 scopus 로고    scopus 로고
    • For recent reviews, see: a
    • For recent reviews, see: (a) Jørgensen, K. A. Synthesis 2003, 1117.
    • (2003) Synthesis , pp. 1117
    • Jørgensen, K.A.1
  • 9
    • 31044438051 scopus 로고    scopus 로고
    • For recent examples of asymmetric Friedel-Crafts alkylation of indole derivatives, see: a
    • For recent examples of asymmetric Friedel-Crafts alkylation of indole derivatives, see: (a) Esquivias, J.; Arrayas, R. G.; Carretero, J. C. Angew. Chem., Int. Ed. 2006, 45, 629.
    • (2006) Angew. Chem., Int. Ed , vol.45 , pp. 629
    • Esquivias, J.1    Arrayas, R.G.2    Carretero, J.C.3
  • 23
    • 34247895388 scopus 로고    scopus 로고
    • 6e has been reported, but enantioselective propargylation has not yet been reported until now. (a) Liu, Z.; Liu, Z.; Shafiq, Z.; Wu, Y.-C.; Wang, D.; Chen, Y.-J. Tetrahedron Lett. 2007, 48, 3963.
    • 6e has been reported, but enantioselective propargylation has not yet been reported until now. (a) Liu, Z.; Liu, Z.; Shafiq, Z.; Wu, Y.-C.; Wang, D.; Chen, Y.-J. Tetrahedron Lett. 2007, 48, 3963.
  • 31
    • 38349108665 scopus 로고    scopus 로고
    • An ORTEP drawing of major enantioisomer of 4 is included in the Supporting Information as Figure S 1
    • An ORTEP drawing of major enantioisomer of 4 is included in the Supporting Information as Figure S 1.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.