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Volumn 55, Issue 6, 2014, Pages 1192-1195

Synthesis of 1-acetyl-2-silyoxycycloheptane derivatives via highly stereoselective formal [5+2] cycloaddition reaction

Author keywords

Cycloaddition reaction; Cycloheptane; Dicobalt acetylene complex; Enol silyl ether

Indexed keywords


EID: 84895011618     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2013.12.102     Document Type: Article
Times cited : (7)

References (13)
  • 1
    • 0000889160 scopus 로고    scopus 로고
    • John Wiley & Sons New York
    • For reviews on [4+3] cycloaddition strategy, see: J.H. Rigby, and F.C. Pigge L.A. Paquette, Organic Reactions 51 1997 John Wiley & Sons New York 351 476
    • (1997) Organic Reactions , vol.51 , pp. 351-476
    • Rigby, J.H.1    Pigge, F.C.2    Paquette, L.A.3
  • 4
    • 79951820592 scopus 로고    scopus 로고
    • For a recent review on [5+2] cycloaddition strategy
    • For a recent review on [5+2] cycloaddition strategy: H. Pellissier Adv. Synth. Catal. 353 2011 189 218
    • (2011) Adv. Synth. Catal. , vol.353 , pp. 189-218
    • Pellissier, H.1
  • 8
    • 84861346900 scopus 로고    scopus 로고
    • For a review on seven-membered dicobalt acetylene complexes, see: J.R. Green Synlett 2012 1271 1282
    • (2012) Synlett , pp. 1271-1282
    • Green, J.R.1
  • 9
    • 79957514567 scopus 로고    scopus 로고
    • This type of transformation is classified as 'time and space integration of reactions' where all reaction components are mixed at once to perform a sequence of reactions in one-pot J. Yoshida, K. Saito, T. Nokami, and A. Nagaki Synlett 2011 1189 1194
    • (2011) Synlett , pp. 1189-1194
    • Yoshida, J.1    Saito, K.2    Nokami, T.3    Nagaki, A.4
  • 10
    • 0025687660 scopus 로고
    • Similar conjugate addition reactions using a zinc acetylide were reported: S. Kim, and J.M. Lee Tetrahedron Lett. 31 1990 7627 7630
    • (1990) Tetrahedron Lett. , vol.31 , pp. 7627-7630
    • Kim, S.1    Lee, J.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.