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Volumn 4, Issue 17, 2002, Pages 2993-2995

Trans-hydrometalation of alkynes by a combination of InCl3 and DIBAL-H: One-pot access to functionalized (Z)-alkenes

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Indexed keywords


EID: 0001464628     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol026401w     Document Type: Article
Times cited : (95)

References (40)
  • 7
    • 0004063249 scopus 로고    scopus 로고
    • VCH: Weinheim, Chapters 3.4 and 6.3
    • (a) Davies A. G. Organotin Chemistry; VCH: Weinheim, 1997, Chapters 3.4 and 6.3.
    • (1997) Organotin Chemistry
    • Davies, A.G.1
  • 12
    • 0000487195 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford
    • (a) Hiyama, T.; Kusumoto, T. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 8, p 763.
    • (1991) Comprehensive Organic Synthesis , vol.8 , pp. 763
    • Hiyama, T.1    Kusumoto, T.2
  • 13
    • 0000829913 scopus 로고
    • Patai, S., Rappoport, Z., Eds.; John Wiley: New York
    • (b) Ojima, I. In The Chemistry of Organic Silicon Compounds; Patai, S., Rappoport, Z., Eds.; John Wiley: New York, 1989, p 1479.
    • (1989) The Chemistry of Organic Silicon Compounds , pp. 1479
    • Ojima, I.1
  • 14
    • 0034709380 scopus 로고    scopus 로고
    • Radical hydrostannylation
    • Rhodium-catalyzed hydroboration. (a) Ohmura, T.; Yamamoto, Y.; Miyaura, N. J. Am. Chem. Soc. 2000, 122, 4990-4991. Radical hydrostannylation,
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 4990-4991
    • Ohmura, T.1    Yamamoto, Y.2    Miyaura, N.3
  • 18
    • 0035915363 scopus 로고    scopus 로고
    • Lewis acid-mediated synthesis of (Z)-alkenylsilanes and -stannanes
    • (e) Trost, B. M.; Ball, Z. T. J. Am. Chem. Soc. 2001, 123, 12726-12727. Lewis acid-mediated synthesis of (Z)-alkenylsilanes and -stannanes,
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 12726-12727
    • Trost, B.M.1    Ball, Z.T.2
  • 24
    • 0004269715 scopus 로고    scopus 로고
    • Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, Chapter 1.2
    • (b) Yorimitsu, H.; Oshima, K. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001, Chapter 1.2.
    • (2001) Radicals in Organic Synthesis
    • Yorimitsu, H.1    Oshima, K.2
  • 26
    • 0033534067 scopus 로고    scopus 로고
    • Indium hydride spontaneously induces radical reaction. See ref 11. Moreover, some organoaluminum compounds can initiate a radical reaction. See, Chakraborty, A.; Marek, I. Chem. Commun. 1999, 2375-2376.
    • (1999) Chem. Commun. , pp. 2375-2376
    • Chakraborty, A.1    Marek, I.2
  • 27
    • 0042871123 scopus 로고    scopus 로고
    • note
    • The hydroindation reaction at 0 °C, -10 °C, and -40 °C yielded a mixture of stereoisomers (E/Z = 20/80, 6/94, and 3/97, respectively) after iodolysis.
  • 40
    • 0042871122 scopus 로고    scopus 로고
    • note
    • 3 (0.015 mmol) in THF (1.0 mL) in another flask.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.