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Volumn 44, Issue 7, 2005, Pages 1075-1078

Alkyne carbonylation by radicals: Tin-radical-catalyzed synthesis of α-methylene amides from 1-alkynes, carbon monoxide, and amines

Author keywords

Alkynes; Amides; Carbonylation; Radical Reactions; Tin

Indexed keywords

AMINES; CARBON MONOXIDE; CARBONYLATION; CATALYSIS; FREE RADICALS; IONS; SYNTHESIS (CHEMICAL);

EID: 15444364760     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200461954     Document Type: Article
Times cited : (138)

References (32)
  • 1
    • 0004269715 scopus 로고    scopus 로고
    • (Eds.: P. Renaud, M. P. Sibi), Wiley-VCH, Weinheim
    • For reviews on radical chemistry, see a) Radicals in Organic Synthesis, Vols. 1 and 2 (Eds.: P. Renaud, M. P. Sibi), Wiley-VCH, Weinheim, 2001;
    • (2001) Radicals in Organic Synthesis, Vols. 1 and 2 , vol.1-2
  • 4
    • 0001024751 scopus 로고    scopus 로고
    • For reviews on radical carbonylations, see a) I. Ryu, N. Sonoda, Angew. Chem. 1996, 108, 1140; Angew. Chem. Int. Ed. Engl. 1996, 35, 1050;
    • (1996) Angew. Chem. , vol.108 , pp. 1140
    • Ryu, I.1    Sonoda, N.2
  • 5
    • 0029790992 scopus 로고    scopus 로고
    • For reviews on radical carbonylations, see a) I. Ryu, N. Sonoda, Angew. Chem. 1996, 108, 1140; Angew. Chem. Int. Ed. Engl. 1996, 35, 1050;
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 1050
  • 30
    • 15444371815 scopus 로고    scopus 로고
    • As for the formation of tin-containing by-product 4a, hydrogen abstraction from 1-hydroxyallyl radical may be a possible reaction course. For a recent mechanistic study on a related system, see A. L. J. Beckwith, V. W. Bowry, W. R. Bowman, E. Mann, J. Parr, J. M. D. Storey, Angew. Chem. 2004, 116, 97; Angew. Chem. Int. Ed. 2004, 43, 95.
    • (2004) Angew. Chem. , vol.116 , pp. 97
    • Beckwith, A.L.J.1    Bowry, V.W.2    Bowman, W.R.3    Mann, E.4    Parr, J.5    Storey, J.M.D.6
  • 31
    • 38849190737 scopus 로고    scopus 로고
    • As for the formation of tin-containing by-product 4a, hydrogen abstraction from 1-hydroxyallyl radical may be a possible reaction course. For a recent mechanistic study on a related system, see A. L. J. Beckwith, V. W. Bowry, W. R. Bowman, E. Mann, J. Parr, J. M. D. Storey, Angew. Chem. 2004, 116, 97; Angew. Chem. Int. Ed. 2004, 43, 95.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 95


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.