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Volumn 14, Issue 3, 2012, Pages 874-877

Au(III)-catalyzed tandem amination - Hydration of alkynes: Synthesis of α-(N -2-pyridonyl)ketones

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EID: 84856714197     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol203398e     Document Type: Article
Times cited : (40)

References (38)
  • 4
  • 5
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    • Arcadi, A. Chem. Rev. 2008, 108, 3266-3325
    • (2008) Chem. Rev. , vol.108 , pp. 3266-3325
    • Arcadi, A.1
  • 6
    • 40949091926 scopus 로고    scopus 로고
    • references therein
    • Shen, H. C. Tetrahedron 2008, 64, 3885-3903 and references therein
    • (2008) Tetrahedron , vol.64 , pp. 3885-3903
    • Shen, H.C.1
  • 23
    • 34249006882 scopus 로고    scopus 로고
    • Addition to the distal position of the alkyne has been observed in Au-catalyzed reactions of propargylic esters; see
    • Addition to the distal position of the alkyne has been observed in Au-catalyzed reactions of propargylic esters; see: Marion, N.; Nolan, S. P. Angew. Chem., Int. Ed. 2007, 46, 2750-2752
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 2750-2752
    • Marion, N.1    Nolan, S.P.2
  • 32
    • 34247877815 scopus 로고    scopus 로고
    • references therein
    • Hashmi, A. S. K. Catal. Today 2007, 122, 211-214 and references therein
    • (2007) Catal. Today , vol.122 , pp. 211-214
    • Hashmi, A.S.K.1
  • 38
    • 0037999818 scopus 로고    scopus 로고
    • Comparable studies on BINOL have shown its barrier to rotation to be 37.8 kcal/mol. See
    • Comparable studies on BINOL have shown its barrier to rotation to be 37.8 kcal/mol. See: Meca, L.; Reha, D.; Havlas, Z. J. Org. Chem. 2003, 68, 5677-5680
    • (2003) J. Org. Chem. , vol.68 , pp. 5677-5680
    • Meca, L.1    Reha, D.2    Havlas, Z.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.