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Volumn 355, Issue 4, 2013, Pages 647-652

Use of a semihollow-shaped triethynylphosphane ligand for efficient formation of six- and seven-membered ring ethers through gold(I)-catalyzed cyclization of hydroxy-tethered propargylic esters

Author keywords

cyclization; gold; propargylic esters; seven membered rings; triethnylphosphane

Indexed keywords


EID: 84874689830     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201200949     Document Type: Article
Times cited : (19)

References (35)
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    • A. Arcadi, Chem. Rev. 2008, 108, 3266-3325
    • (2008) Chem. Rev. , vol.108 , pp. 3266-3325
    • Arcadi, A.1
  • 24
    • 70349782130 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 3112-3115
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 3112-3115
  • 35
    • 72449148698 scopus 로고    scopus 로고
    • To the best of our knowledge, gold-catalyzed hydroalkoxylation of alkenes, allenes and alkynes in a 7-exo manner has not been reported. For examples of gold-catalyzed 7-endo-dig hydroalkoxylation of alkynes, see:, K. Wilckens, M. Uhlemann, C. Czekelius, Chem. Eur. J. 2009, 15, 13323-13326.
    • (2009) Chem. Eur. J. , vol.15 , pp. 13323-13326
    • Wilckens, K.1    Uhlemann, M.2    Czekelius, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.