메뉴 건너뛰기




Volumn 13, Issue 2, 2015, Pages 520-526

Trifluoromethanesulfonyloxy-group-directed regioselective (3 + 2) cycloadditions of benzynes for the synthesis of functionalized benzo-fused heterocycles

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOADDITION;

EID: 84918576679     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c4ob01627k     Document Type: Article
Times cited : (44)

References (71)
  • 43
    • 33751424969 scopus 로고    scopus 로고
    • For a related benzyne precursor, see
    • G. Zeni R. C. Larock Chem. Rev. 2006 106 4644 4680
    • (2006) Chem. Rev. , vol.106 , pp. 4644-4680
    • Zeni, G.1    Larock, R.C.2
  • 56
    • 79251486518 scopus 로고    scopus 로고
    • Gaussian, Inc., Wallingford, CT
    • M. J. Frisch, et al., Gaussian, Inc., Wallingford, CT, 2009
    • (2009) Et Al.
    • Frisch, M.J.1
  • 63
    • 84887495959 scopus 로고    scopus 로고
    • th NBO (Fig. 1) Distortion analysis 21 could also rationalize the regioselectivities of (3 + 2) cycloaddition of 3-substituted benzynes 3c and 3d; however, this method could not be applied to the reactions of 4-substituted benzynes 3e and 3f (see the ESI) Recently, Houk and Garg et al. have proposed that distortions of arynes are useful to predict and understand the regioselectivities of aryne reactions, see
    • A. Takagi T. Ikawa K. Saito S. Masuda T. Ito S. Akai Org. Biomol. Chem. 2013 11 8145 8150
    • (2013) Org. Biomol. Chem. , vol.11 , pp. 8145-8150
    • Takagi, A.1    Ikawa, T.2    Saito, K.3    Masuda, S.4    Ito, T.5    Akai, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.