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Volumn 51, Issue 38, 2012, Pages 9610-9614

Cobalt-catalyzed addition of arylzinc reagents to alkynes to form ortho-alkenylarylzinc species through 1,4-cobalt migration

Author keywords

alkynes; C H activation; cobalt; multicomponent couplings; organozinc reagents

Indexed keywords

ALKYNES; ARYLZINC REAGENTS; C-H ACTIVATION; CARBOMETALATION; ELECTROPHILES; FUNCTIONALIZED; INTERNAL ALKYNES; MULTI-COMPONENT COUPLING; ORGANOZINC REAGENTS; TRANSMETALATION;

EID: 84866402318     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201204388     Document Type: Article
Times cited : (106)

References (63)
  • 44
    • 33846064670 scopus 로고    scopus 로고
    • The most acidic positions of thiophene and quinoline are C2 and C4, respectively.
    • The most acidic positions of thiophene and quinoline are C2 and C4, respectively:, K. Shen, Y. Fu, J.-N. Li, L. Liu, Q.-X. Guo, Tetrahedron 2007, 63, 1568.
    • (2007) Tetrahedron , vol.63 , pp. 1568
    • Shen, K.1    Fu, Y.2    Li, J.-N.3    Liu, L.4    Guo, Q.-X.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.