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Volumn 52, Issue 34, 1996, Pages 11215-11238

Synthesis of optically active β,γ-alkynylglycine derivatives

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNE DERIVATIVE; GLYCINE DERIVATIVE;

EID: 0030593682     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00630-8     Document Type: Article
Times cited : (45)

References (107)
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    • 1. Presented in part at the 4th International Congress on Aminoacids, Vienna, August 7-11, 1995 ; abstract paper in Amino Acids 1995, 9, 73.
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  • 2
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    • 1. Presented in part at the 4th International Congress on Aminoacids, Vienna, August 7-11, 1995 ; abstract paper in Amino Acids 1995, 9, 73.
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  • 11
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    • i) Walsh, C. Tetrahedron 1982, 38, 871-909.
    • (1982) Tetrahedron , vol.38 , pp. 871-909
    • Walsh, C.1
  • 17
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    • Organic Chemistry Series Baldwin J. E. ; Magnus P. D. Eds, Pergamon Press: New-York
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    • (1989) Synthesis of Optically Active α-aminoacids , vol.7
    • Williams, R.M.1
  • 29
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    • Proceedings of the 5th Cyprus Conference on New methods in Drug Design, 1992
    • Makriyannis, A.; Castagnoli, N. Eds ; J. R. Prous Science Publishers S. A., in press
    • d) Duthaler, R. O.; Hafner, A. Proceedings of the 5th Cyprus Conference on New methods in Drug Design, 1992, In New Methods in Drug Research, Volume 4 ; Makriyannis, A.; Castagnoli, N. Eds ; J. R. Prous Science Publishers S. A., 1994, in press.
    • (1994) New Methods in Drug Research , vol.4
    • Duthaler, R.O.1    Hafner, A.2
  • 39
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    • For another convenient, large scale preparation of 5 see also ref.40
    • f) For another convenient, large scale preparation of 5 see also ref.40
  • 43
    • 0029876160 scopus 로고    scopus 로고
    • c) Reginato, G.; Mordini, A.; Degl'Innocenti, A.; Caracciolo, M. Tetrahedron Lett. 1995, 36, 8275-8278 and ibid. 1996, 37, 1325.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 1325
  • 47
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    • 12. a) Gilbert, J. C. ; Weerasooriya, U. J. Org. Chem. 1982, 47, 1837-1845. b) ibid. 1979, 44, 4997-4998.
    • (1979) J. Org. Chem. , vol.44 , pp. 4997-4998
  • 54
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    • For another one-step efficient aldehyde-to-alkyne transformation : a
    • 16. For another one-step efficient aldehyde-to-alkyne transformation see : a) Ohira, S.; Okai, K.; Moritani, T. J. Chem. Soc. Chem. Commun. 1992, 721-722.
    • (1992) J. Chem. Soc. Chem. Commun. , pp. 721-722
    • Ohira, S.1    Okai, K.2    Moritani, T.3
  • 57
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    • Same type of by-products have been noticed under the same conditions: see ref. 10c.
    • 18. Same type of by-products have been noticed under the same conditions: see ref. 10c.
  • 64
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    • Formation of 13 has already been described from a close analogue of 6b but via a different route
    • 23. Formation of 13 has already been described from a close analogue of 6b but via a different route : Renaud, P. ; Seebach, D. Angew. Chem. Int. Ed. Engl. 1986, 25, 843-844.
    • (1986) Angew. Chem. Int. Ed. Engl. , vol.25 , pp. 843-844
    • Renaud, P.1    Seebach, D.2
  • 95
    • 85030279851 scopus 로고    scopus 로고
    • 43. a) Cainelli, G. ; Cardillo, G. Chromium oxidation in Organic Chemistry, Springer-Verlag : New-York. 1984; pp. 118-151. b) ibid.; pp 204-209.
    • Chromium Oxidation in Organic Chemistry , pp. 204-209
  • 100
    • 85030269041 scopus 로고    scopus 로고
    • 17 failed because of the presence of electron withdrawing substituents on the double bond and subsequent enolization of intermediate aldehydes
    • 17 failed because of the presence of electron withdrawing substituents on the double bond and subsequent enolization of intermediate aldehydes.
  • 101
    • 85030269914 scopus 로고    scopus 로고
    • formula presented
    • (formula presented)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.