메뉴 건너뛰기




Volumn 81, Issue 14, 2016, Pages 5998-6006

Decreasing Distortion Energies without Strain: Diazo-Selective 1,3-Dipolar Cycloadditions

Author keywords

[No Author keywords available]

Indexed keywords

CHEMISTRY; ORGANIC COMPOUNDS;

EID: 84978663216     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/acs.joc.6b00948     Document Type: Article
Times cited : (27)

References (114)
  • 52
    • 84903288731 scopus 로고    scopus 로고
    • For a tutorial review of the distortion/interaction model (which is also known as the activation strain model), see
    • For a tutorial review of the distortion/interaction model (which is also known as the activation strain model), see: Fernández, I.; Bickelhaupt, F. M. Chem. Soc. Rev. 2014, 43, 4953-4967 10.1039/c4cs00055b
    • (2014) Chem. Soc. Rev. , vol.43 , pp. 4953-4967
    • Fernández, I.1    Bickelhaupt, F.M.2
  • 56
  • 66
    • 0000288714 scopus 로고
    • Leffler, J. E. Science 1953, 117, 340-341 10.1126/science.117.3039.340
    • (1953) Science , vol.117 , pp. 340-341
    • Leffler, J.E.1
  • 68
    • 49649159600 scopus 로고
    • Sustmann, R. Tetrahedron Lett. 1971, 12, 2717-2720 10.1016/S0040-4039(01)96961-8
    • (1971) Tetrahedron Lett. , vol.12 , pp. 2717-2720
    • Sustmann, R.1
  • 70
  • 74
    • 84861843694 scopus 로고    scopus 로고
    • Distortion of dipolarophiles also decreases the gap in FMO energies between reacting partners, thereby decreasing dipole distortion indirectly by favoring an early TS
    • Distortion of dipolarophiles also decreases the gap in FMO energies between reacting partners, thereby decreasing dipole distortion indirectly by favoring an early TS. Gordon, C. G.; Mackey, J. L.; Jewett, J. C.; Sletten, E. M.; Houk, K. N.; Bertozzi, C. R. J. Am. Chem. Soc. 2012, 134, 9199-9208 10.1021/ja3000936
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 9199-9208
    • Gordon, C.G.1    Mackey, J.L.2    Jewett, J.C.3    Sletten, E.M.4    Houk, K.N.5    Bertozzi, C.R.6
  • 75
    • 84876521192 scopus 로고    scopus 로고
    • In addition, the present study uses the M06-2X level of theory, which has proven to be better suited for asynchronous cycloadditions
    • In addition, the present study uses the M06-2X level of theory, which has proven to be better suited for asynchronous cycloadditions. Linder, M.; Brinck, T. Phys. Chem. Chem. Phys. 2013, 15, 5108-5114 10.1039/c3cp44319a
    • (2013) Phys. Chem. Chem. Phys. , vol.15 , pp. 5108-5114
    • Linder, M.1    Brinck, T.2
  • 91
    • 67849087099 scopus 로고    scopus 로고
    • Bach, R. D. J. Am. Chem. Soc. 2009, 131, 5233-5243 10.1021/ja8094137
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 5233-5243
    • Bach, R.D.1
  • 95
    • 0009362503 scopus 로고
    • Huisgen, R. Pure Appl. Chem. 1980, 52, 2283-2302 10.1351/pac198052102283
    • (1980) Pure Appl. Chem. , vol.52 , pp. 2283-2302
    • Huisgen, R.1
  • 96


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.