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Volumn 129, Issue 9, 2007, Pages 2691-2699

The participation of alkynylboronates in inverse electron demand [4 + 2] cycloadditions: A mechanistic study

Author keywords

[No Author keywords available]

Indexed keywords

ELECTRON BEAMS; OLEFINS; PHASE TRANSITIONS; PROBABILITY DENSITY FUNCTION; REACTION KINETICS;

EID: 33847611084     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja068527k     Document Type: Article
Times cited : (64)

References (77)
  • 1
    • 27644475970 scopus 로고    scopus 로고
    • Hall, D. G, Ed, Wiley-VCH: Weinheim
    • Boronic Acids; Hall, D. G., Ed.; Wiley-VCH: Weinheim, 2005.
    • (2005) Boronic Acids
  • 10
    • 23944465006 scopus 로고    scopus 로고
    • For recent overviews see: a
    • For recent overviews see: (a) Hilt, G.; Bolze, P. Synthesis 2005, 2091.
    • (2005) Synthesis , pp. 2091
    • Hilt, G.1    Bolze, P.2
  • 37
    • 0142258275 scopus 로고    scopus 로고
    • For DFT calculations on the participation of alkynylboronates in [3 + 2] cycloadditions, see: Saez, J. A.; Arno, M.; Domingo, L. R. Tetrahedron 2003, 59, 9167.
    • For DFT calculations on the participation of alkynylboronates in [3 + 2] cycloadditions, see: Saez, J. A.; Arno, M.; Domingo, L. R. Tetrahedron 2003, 59, 9167.
  • 41
    • 33847628655 scopus 로고    scopus 로고
    • Gaussian, Inc, Wallingford CT
    • Frisch, M. J.; et al. Gaussian 03, revision C.02; Gaussian, Inc.: Wallingford CT, 2004.
    • (2004) Gaussian 03, revision , Issue.C.02
    • Frisch, M.J.1
  • 58
    • 33847660325 scopus 로고    scopus 로고
    • In preliminary studies we could actually locate related [4, 2] and [4, 3] transition states for the reaction between 5 and cyclopentadiene
    • In preliminary studies we could actually locate related [4 + 2] and [4 + 3] transition states for the reaction between 5 and cyclopentadiene.
  • 60
    • 0032509454 scopus 로고    scopus 로고
    • For DFT studies on the participation of acetylene dicarboxylates in cycloaddition reactions, see: a
    • For DFT studies on the participation of acetylene dicarboxylates in cycloaddition reactions, see: (a) Domingo, L. R.; Picher, M. T.; Zaragoza, R. J. J. Org. Chem. 1998, 63, 9183.
    • (1998) J. Org. Chem , vol.63 , pp. 9183
    • Domingo, L.R.1    Picher, M.T.2    Zaragoza, R.J.3
  • 76
    • 0037613350 scopus 로고    scopus 로고
    • The weak nucleophilicity of 9 along with the symmetry of tetraazine are responsible for the low polar character of this cycloaddition: Domingo, L. R.; Aurell, M. J.; Perez, P.; Contreras, R. J. Org. Chem. 2003, 68, 3884.
    • The weak nucleophilicity of 9 along with the symmetry of tetraazine are responsible for the low polar character of this cycloaddition: Domingo, L. R.; Aurell, M. J.; Perez, P.; Contreras, R. J. Org. Chem. 2003, 68, 3884.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.