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Volumn 69, Issue 22, 2004, Pages 7592-7598

Synthesis of allylsilanes by reductive lithiation of thioethers

Author keywords

[No Author keywords available]

Indexed keywords

SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

EID: 6344221782     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo049237u     Document Type: Article
Times cited : (23)

References (38)
  • 3
    • 0003688276 scopus 로고    scopus 로고
    • and previous articles of these series
    • (c) Fraga, B. M. Nat. Prod. Rep. 2003, 392-413 and previous articles of these series.
    • (2003) Nat. Prod. Rep. , pp. 392-413
    • Fraga, B.M.1
  • 16
    • 0000609087 scopus 로고
    • Regio- and stereoselective reductive silylation by a siloxy or hydroxyl group has been reported: Marumoto, S.; Kuwajima, I. J. Am. Chem. Soc. 1993, 115, 9021-9024.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 9021-9024
    • Marumoto, S.1    Kuwajima, I.2
  • 26
    • 0026589720 scopus 로고
    • THF cleavage can also be achieved with a catalytic amount of DBB or naphthalene, see: (b) Ramon, D. J.; Yus, M. Tetrahedron 1992, 48, 3585-3588.
    • (1992) Tetrahedron , vol.48 , pp. 3585-3588
    • Ramon, D.J.1    Yus, M.2
  • 27
    • 6344271048 scopus 로고
    • For other synthetic applications of THF cleavage, see: (c) Oikawa, M.; Oikawa, H.; Ichihara, A. Tetrahedron 1995, 51, 11457-11464.
    • (1995) Tetrahedron , vol.51 , pp. 11457-11464
    • Oikawa, M.1    Oikawa, H.2    Ichihara, A.3
  • 32
    • 0001820427 scopus 로고    scopus 로고
    • THF derivatives substituted by a vinyl moiety undergo a smooth reductive lithiation under mild condition, see ref 12a. For reviews on the reductive cleavage of small ring heterocycles, see ref 4b, and: Yus, M.; Foubelo, F. Rev. Heteroatom Chem. 1997, 17, 73-107.
    • (1997) Rev. Heteroatom Chem. , vol.17 , pp. 73-107
    • Yus, M.1    Foubelo, F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.