메뉴 건너뛰기




Volumn 1992, Issue 12, 1992, Pages 943-961

New Mechanistic Insights into Reductions of Halides and Radicals with Samarium(II) Iodide

Author keywords

[No Author keywords available]

Indexed keywords


EID: 85022594998     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-1992-21544     Document Type: Article
Times cited : (315)

References (134)
  • 1
    • 0000104215 scopus 로고
    • Recent reviews and overviews: a, Trost, B. M.; Fleming, I.; Eds.; Pergamon: Oxford
    • Recent reviews and overviews: (a) Molander, G. A. In Comp. Org. Syn.; Trost, B. M.; Fleming, I.; Eds.; Pergamon: Oxford, 1991, Vol. 4, pp. 251-282.
    • (1991) Comp. Org. Syn. , vol.4 , pp. 251-282
    • Molander, G.A.1
  • 24
    • 0001411041 scopus 로고
    • Tetrahedron Lett. 1989, 30, 3681.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 3681
  • 38
    • 0642299055 scopus 로고
    • Recent leading references: a
    • Recent leading references: (a) Molander, G. A.; Kenny, C. J. Org. Chem. 1988, 53, 2132.
    • (1988) J. Org. Chem. , vol.53 , pp. 2132
    • Molander, G.A.1    Kenny, C.2
  • 82
    • 0000392657 scopus 로고
    • Molander and Harring have recently reported some related cyclizations under the traditional samarium Barbier procedure
    • (c) Molander and Harring have recently reported some related cyclizations under the traditional samarium Barbier procedure. Molander, G. A.; Harring, L. S. J. Org. Chem. 1990, 55, 6171.
    • (1990) J. Org. Chem. , vol.55 , pp. 6171
    • Molander, G.A.1    Harring, L.S.2
  • 86
    • 0013533698 scopus 로고
    • For example, it has been known for 25 years that diamines increase the reduction potential of low-valent chromium reagents. Kochi, J. K.; Mocadlo, P. E. J. Am. Chem. Soc. 1966, 88, 4094.
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 4094
    • Kochi, J.K.1    Mocadlo, P.E.2
  • 89
    • 0002041589 scopus 로고
    • Radical additions to ketones are usually followed by rapid cleavages
    • Radical additions to ketones are usually followed by rapid cleavages. Dowd, P.; Choi, S.-C. Tetrahedron 1989, 45, 77.
    • (1989) Tetrahedron , vol.45 , pp. 77
    • Dowd, P.1    Choi, S.-C.2
  • 103
    • 0003952404 scopus 로고
    • Bard, A. J.; Lund, H., Eds.; Dekker: NY, and
    • (b) Encyclopedia of Electrochemistry of the Elements; Bard, A. J.; Lund, H., Eds.; Dekker: NY, 1980, Volumes XII and XIV.
    • (1980) Encyclopedia of Electrochemistry of the Elements , vol.12-14
  • 106
  • 107
    • 85064400496 scopus 로고
    • Transition metal alkyls in branched or crowded environments have much weaker bonds compared to primary alkyl derivatives
    • (b) Transition metal alkyls in branched or crowded environments have much weaker bonds compared to primary alkyl derivatives. Connor, J. A. Top. Curr. Chem. 1977, 71, 71.
    • (1977) Connor, J. A. Top. Curr. Chem. , vol.71 , pp. 71
  • 128
    • 0001216647 scopus 로고
    • Trost, B. M.; Fleming, I. Eds.; Pergamon: Oxford, Ch.4, 779
    • Curran, D. P. Comp. Org. Syn:, Trost, B. M.; Fleming, I. Eds.; Pergamon: Oxford, 1991, Ch.4, pp. 715, 779.
    • (1991) Comp. Org. Syn , pp. 715
    • Curran, D.P.1
  • 134
    • 0026059141 scopus 로고
    • From alkynyl and alkenyl cyclopropyl ketones
    • (b) From alkynyl (and alkenyl) cyclopropyl ketones: Batey, R. A.; Motherwell, W. B. Tetrahedron Lett. 1991, 32, 6211.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 6211
    • Batey, R.A.1    Motherwell, W.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.