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Volumn , Issue 5, 1998, Pages 409-410

The substituent effect on stereoselective reductive lithiation of 4,5-disubstituted 2-phenylthiooxolane

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EID: 0032364527     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1998.409     Document Type: Article
Times cited : (7)

References (26)
  • 1
    • 0021981588 scopus 로고
    • For example, pectenotoxins; T. Yasumoto, M. Murata, Y. Oshima, M. Sano, G. K. Matsumoto, and J. Clardy, Tetrahedron, 41, 1019 (1985), laureoxolane; A. Fukuzawa, M. Aye, Y. Takaya, H. Fukui, T. Masamune, and A. Murai, Tetrahedron Lett., 30, 3665 (1989), parvifolorin; S. Ratnayake, Z. Gu, L. R. Miesbauer, D. L. Smith, K. V. Wood, D. R. Evert, and J. L. MacLaughlin, Can. J. Chem., 72, 287 (1994), and so on.
    • (1985) Tetrahedron , vol.41 , pp. 1019
    • Yasumoto, T.1    Murata, M.2    Oshima, Y.3    Sano, M.4    Matsumoto, G.K.5    Clardy, J.6
  • 2
    • 0041457208 scopus 로고
    • For example, pectenotoxins; T. Yasumoto, M. Murata, Y. Oshima, M. Sano, G. K. Matsumoto, and J. Clardy, Tetrahedron, 41, 1019 (1985), laureoxolane; A. Fukuzawa, M. Aye, Y. Takaya, H. Fukui, T. Masamune, and A. Murai, Tetrahedron Lett., 30, 3665 (1989), parvifolorin; S. Ratnayake, Z. Gu, L. R. Miesbauer, D. L. Smith, K. V. Wood, D. R. Evert, and J. L. MacLaughlin, Can. J. Chem., 72, 287 (1994), and so on.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 3665
    • Fukuzawa, A.1    Aye, M.2    Takaya, Y.3    Fukui, H.4    Masamune, T.5    Murai, A.6
  • 3
    • 0028329475 scopus 로고
    • and so on
    • For example, pectenotoxins; T. Yasumoto, M. Murata, Y. Oshima, M. Sano, G. K. Matsumoto, and J. Clardy, Tetrahedron, 41, 1019 (1985), laureoxolane; A. Fukuzawa, M. Aye, Y. Takaya, H. Fukui, T. Masamune, and A. Murai, Tetrahedron Lett., 30, 3665 (1989), parvifolorin; S. Ratnayake, Z. Gu, L. R. Miesbauer, D. L. Smith, K. V. Wood, D. R. Evert, and J. L. MacLaughlin, Can. J. Chem., 72, 287 (1994), and so on.
    • (1994) Can. J. Chem. , vol.72 , pp. 287
    • Ratnayake, S.1    Gu, Z.2    Miesbauer, L.R.3    Smith, D.L.4    Wood, K.V.5    Evert, D.R.6    MacLaughlin, J.L.7
  • 5
    • 0028238636 scopus 로고
    • Quayle's group has developed a method for diastereoselective synthesis of 3-substituted 2-stannyloxolane and demonstrated its tin-lithium transmetalation. The availability of the method for other oxolane system is unknown. a) Y. Zhao, R. L. Beddoes, and P. Quayle, Tetrahedron Lett., 35, 4183 (1994).
    • (1994) Tetrahedron Lett. , vol.35 , pp. 4183
    • Zhao, Y.1    Beddoes, R.L.2    Quayle, P.3
  • 18
    • 0042960186 scopus 로고    scopus 로고
    • note
    • The stereochemistries of 12 and 13 were determined by NOEs. That of 11 could be determined by NOEs of 11' derived from 11. formula presented
  • 19
    • 0042459109 scopus 로고    scopus 로고
    • note
    • It is to be noted that the ratios of the products were slightly different depending upon the electrophiles.
  • 20
    • 0042960185 scopus 로고    scopus 로고
    • note
    • Absence of the equilibrium in 3-substituted 2-lithiooxolane system at -78 °C has been reported by Quayle. See ref 3a.
  • 24
    • 0042459097 scopus 로고    scopus 로고
    • note
    • In each case, the ratio was determined by HPLC analysis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.