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Volumn 51, Issue 42, 2015, Pages 8769-8772

Tuning radical reactivity using iodine in oxidative C(sp3)-H/C(sp)-H cross-coupling: An easy way toward the synthesis of furans and indolizines

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; FURAN DERIVATIVE; HYDROGEN; INDOLIZINE DERIVATIVE; IODINE;

EID: 84929191018     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c5cc01825k     Document Type: Article
Times cited : (111)

References (69)
  • 45
    • 84858146264 scopus 로고    scopus 로고
    • in, ed. M. Heinrich and A. Gansäuer, Springer, Berlin, Heidelberg, 320
    • U. Jahn, in Radicals in Synthesis III, ed., M. Heinrich, and, A. Gansäuer, Springer, Berlin, Heidelberg, 2012, vol. 320, pp. 191-322
    • (2012) Radicals in Synthesis III , pp. 191-322
    • Jahn, U.1
  • 65
    • 30344438843 scopus 로고    scopus 로고
    • Internal alkynes were unreactive in the iodine catalysis system. A mechanistic study of the formation of silver-mediated furan explained that the transformation of internal alkynes proceeds through higher barriers during radical addition than that of terminal alkynes. In addition, the reaction with internal alkynes was also less favorable thermodynamically. See ref. 13b
    • H. M. Meshram P. N. Reddy P. Vishnu K. Sadashiv J. S. Yadav Tetrahedron Lett. 2006 47 991 995
    • (2006) Tetrahedron Lett. , vol.47 , pp. 991-995
    • Meshram, H.M.1    Reddy, P.N.2    Vishnu, P.3    Sadashiv, K.4    Yadav, J.S.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.