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Volumn , Issue 12, 1995, Pages 1245-1246

The first example of enantioselective carbenoid addition to organochalcogen atoms: Application to [2,3]sigmatropic rearrangement of allylic chalcogen ylides

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Indexed keywords


EID: 37049073009     PISSN: 00224936     EISSN: None     Source Type: Journal    
DOI: 10.1039/C39950001245     Document Type: Article
Times cited : (94)

References (24)
  • 10
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    • For example, and references cited therein
    • For example: J. Salaiin, Chem. Rev., 1989, 89, 1247 and references cited therein.
    • (1989) Chem. Rev , vol.89 , pp. 1247
    • Salaiin, J.1
  • 17
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    • See for example, and references cited therein
    • See for example: A. Pfaltz, Acc Chem. Res., 1993, 26, 339 and references cited therein.
    • (1993) Acc Chem. Res , vol.26 , pp. 339
    • Pfaltz, A.1
  • 20
    • 18444417883 scopus 로고
    • The ylide formation by the reaction of carbenes or carbenoids with organoheteroatom compounds has been reviewed
    • The ylide formation by the reaction of carbenes or carbenoids with organoheteroatom compounds has been reviewed. M.P. Doyle, Chem. Rev., 1986, 86, 919.
    • (1986) Chem. Rev , vol.86 , pp. 919
    • Doyle, M.P.1
  • 21
    • 0000936734 scopus 로고
    • references cited therein
    • A. Padwa and S.F. Hornbuckle, Chem. Rev., 1991, 91, 263 and references cited therein.
    • (1991) Chem. Rev , vol.91 , pp. 263
    • Padwa, A.1    Hornbuckle, S.F.2
  • 22
    • 0001041059 scopus 로고
    • In the case of asymmetric oxidation of prochiral aryl selenides with sharpless oxidant, the selectivity was much improved by introduction of these substituents into the aryl group
    • In the case of asymmetric oxidation of prochiral aryl selenides with Sharpless oxidant, the selectivity was much improved by introduction of these substituents into the aryl group. N. Komatsu, T. Murakami, Y. Nishibayashi, T. Sugita and S. Uemura, J. Org. Chem., 1993, 58, 3697.
    • (1993) J. Org. Chem , vol.58 , pp. 3697
    • Komatsu, N.1    Murakami, T.2    Nishibayashi, Y.3    Sugita, T.4    Uemura, S.5
  • 24
    • 37049081574 scopus 로고
    • The chiral selenium ylides were extremely stable toward thermal inversion (Racemization by pyramidal inversion) in comparison with similar sulfur ylides
    • The chiral selenium ylides were extremely stable toward thermal inversion (racemization by pyramidal inversion) in comparison with similar sulfur ylides. N. Kamigata, Y. Nakamura, K. Kikuchi, I. Ikemoto, T. Shimizu and H. Matsuyama, J. Chem. Soc, Perkin Trans. 1, 1992, 1721.
    • (1992) J. Chem. Soc, Perkin Trans. 1 , pp. 1721
    • Kamigata, N.1    Nakamura, Y.2    Kikuchi, K.3    Ikemoto, I.4    Shimizu, T.5    Matsuyama, H.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.