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Volumn , Issue 8, 2009, Pages 1221-1227

Molybdenum-catalyzed α-hydrostannations of propargylamines as the key step in the synthesis of N-heterocycles

Author keywords

Hydrostannation; Indoles; Molybdenum; Nitrogen heterocycles; Stannanes; Stille couplings

Indexed keywords


EID: 62249113573     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200801157     Document Type: Article
Times cited : (19)

References (38)
  • 10
    • 17744395347 scopus 로고    scopus 로고
    • and references cited therein
    • b) B. M. Trost, Z. T. Ball, Synthesis 2005, 853-887, and references cited therein.
    • (2005) Synthesis , pp. 853-887
    • Trost, B.M.1    Ball, Z.T.2
  • 32
    • 34250728472 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 4570-4573.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 4570-4573
  • 38
    • 62249125012 scopus 로고    scopus 로고
    • Stille couplings of vinylstannanes generally proceed with retention of the olefin geometry. In the case of the (E)-β-stannylated products formed here, an intramolecular Stille coupling would give rise to a 6-membered ring with an (E) double bond.
    • Stille couplings of vinylstannanes generally proceed with retention of the olefin geometry. In the case of the (E)-β-stannylated products formed here, an intramolecular Stille coupling would give rise to a 6-membered ring with an (E) double bond.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.