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Volumn 79, Issue 3, 2014, Pages 1344-1355

Arynes double bond insertion/nucleophilic addition with vinylogous amides and carbodiimides

Author keywords

[No Author keywords available]

Indexed keywords

ALKENES; AMIDES; CARBODIIMIDES; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 84893838483     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo402754d     Document Type: Article
Times cited : (41)

References (40)
  • 6
    • 0011953642 scopus 로고
    • Complex bases and complex reducing agents: New tools in organic synthesis
    • For an overview of early work, see
    • For an overview of early work, see: Caubére, P. Complex bases and complex reducing agents: New tools in organic synthesis Top. Curr. Chem. 1978, 73, 49-103
    • (1978) Top. Curr. Chem. , vol.73 , pp. 49-103
    • Caubére, P.1
  • 7
    • 84874258232 scopus 로고    scopus 로고
    • For a review of recent advances where ketene acetals or silyl ketene acetals are used, see
    • For a review of recent advances where ketene acetals or silyl ketene acetals are used, see: Flores-Gaspar, A.; Martin, R. Synthesis 2013, 45, 563
    • (2013) Synthesis , vol.45 , pp. 563
    • Flores-Gaspar, A.1    Martin, R.2
  • 17
    • 80052763053 scopus 로고    scopus 로고
    • A formal insertion into C=S double bonds
    • A formal insertion into C=S double bonds: Biswas, K.; Greaney, M. F. Org. Lett. 2011, 13, 4946
    • (2011) Org. Lett. , vol.13 , pp. 4946
    • Biswas, K.1    Greaney, M.F.2
  • 23
    • 33947581843 scopus 로고    scopus 로고
    • This β-arylation is known for related substrates; see ref 2c and
    • This β-arylation is known for related substrates; see ref 2c and Ramtohul, Y. K.; Chartrand, A. Org. Lett. 2007, 9, 1029
    • (2007) Org. Lett. , vol.9 , pp. 1029
    • Ramtohul, Y.K.1    Chartrand, A.2
  • 35
    • 84864068038 scopus 로고    scopus 로고
    • The aryne C-N single bond insertion may be accompanied by other events. For example, we have found that a five-membered cyclic carbamate undergoes epoxide extrusion during the C-N insertion process
    • The aryne C-N single bond insertion may be accompanied by other events. For example, we have found that a five-membered cyclic carbamate undergoes epoxide extrusion during the C-N insertion process: Fang, Y.; Rogness, D. C.; Larock, R. C.; Shi, F. J. Org. Chem. 2012, 77, 6262
    • (2012) J. Org. Chem. , vol.77 , pp. 6262
    • Fang, Y.1    Rogness, D.C.2    Larock, R.C.3    Shi, F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.