메뉴 건너뛰기




Volumn 9, Issue 10, 1998, Pages 1703-1712

Stereoselective synthesis of α-substituted serines from protected erythrulose oximes

Author keywords

[No Author keywords available]

Indexed keywords

ORGANOLITHIUM COMPOUND; OXIME DERIVATIVE; SERINE DERIVATIVE;

EID: 0032557720     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(98)00146-3     Document Type: Article
Times cited : (28)

References (69)
  • 6
    • 0028130028 scopus 로고
    • (d)
    • (d) Cole, D. C. Tetrahedron 1994, 50, 9517-9582.
    • (1994) Tetrahedron , vol.50 , pp. 9517-9582
    • Cole, D.C.1
  • 12
    • 0030955088 scopus 로고    scopus 로고
    • For a recent, short review on the topic of α,α-disubstituted α-amino acids, see:
    • For a recent, short review on the topic of α,α-disubstituted α-amino acids, see: Wirth, T. Angew. Chem. Int. Ed. Engl. 1997, 36, 225-227.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 225-227
    • Wirth, T.1
  • 14
    • 0025319387 scopus 로고
    • For the synthesis of peptides containing such types of amino acids, see: (a)
    • For the synthesis of peptides containing such types of amino acids, see: (a) Wipf, P.; Heimgartner, H. Helv. Chim. Acta 1990, 73, 13-24.
    • (1990) Helv. Chim. Acta , vol.73 , pp. 13-24
    • Wipf, P.1    Heimgartner, H.2
  • 47
    • 0344451844 scopus 로고    scopus 로고
    • (c) Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann E., Eds.; Georg Thieme Verlag: Stuttgart
    • (c) Kunz, H. In Houben-Weyl's Methods of Organic Chemistry, Stereoselective Synthesis; Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann E., Eds.; Georg Thieme Verlag: Stuttgart, 1996; Vol. 3, pp. 1931-1952.
    • (1996) In Houben-Weyl's Methods of Organic Chemistry, Stereoselective Synthesis , vol.3 , pp. 1931-1952
    • Kunz, H.1
  • 49
    • 0012963845 scopus 로고    scopus 로고
    • 16b For the synthesis of α,α-disubstituted α-amino acids based on this methodology, see Ref. 11a and: (a)
    • 16b For the synthesis of α,α-disubstituted α-amino acids based on this methodology, see Ref. 11a and: (a) Harwood, L. M.; Vines, K. J.; Drew, M. G. B. Synlett 1996, 1051-1053.
    • (1996) Synlett , pp. 1051-1053
    • Harwood, L.M.1    Vines, K.J.2    Drew, M.G.B.3
  • 51
    • 0031562473 scopus 로고    scopus 로고
    • (a) Ph.D. Thesis, Univ. Jaume I
    • (a) Murga, J., Ph.D. Thesis, Univ. Jaume I, 1996. For a preliminary account, see: Marco, J. A.; Carda, M.; Murga, J.; González, F.; Falomir, E. Tetrahedron Lett. 1997, 38, 1841-1844. The melting points reported in this paper for 2-methyl serine and 2-phenylserine were erroneously interchanged.
    • (1996)
    • Murga, J.1
  • 52
    • 0031562473 scopus 로고    scopus 로고
    • For a preliminary account, see: The melting points reported in this paper for 2-methyl serine and 2-phenylserine were erroneously interchanged
    • (a) Murga, J., Ph.D. Thesis, Univ. Jaume I, 1996. For a preliminary account, see: Marco, J. A.; Carda, M.; Murga, J.; González, F.; Falomir, E. Tetrahedron Lett. 1997, 38, 1841-1844. The melting points reported in this paper for 2-methyl serine and 2-phenylserine were erroneously interchanged.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 1841-1844
    • Marco, J.A.1    Carda, M.2    Murga, J.3    González, F.4    Falomir, E.5
  • 54
    • 0344883643 scopus 로고    scopus 로고
    • 16b but the conversion of the obtained products into α-t-butyl serine and α-allyl serine has not yet been accomplished
    • 16b but the conversion of the obtained products into α-t-butyl serine and α-allyl serine has not yet been accomplished.
  • 56
    • 0021149831 scopus 로고
    • Cleavage of acetonides (-)-14 and (-)-21 under the aqueous acidic conditions used for (-)-7 provided not only the desired diols but also products of internal transacylation (oxazolidinone migration)
    • Williams, D. R.; Sit, S.-Y. J. Am. Chem. Soc. 1984, 106, 2949-2954. Cleavage of acetonides (-)-14 and (-)-21 under the aqueous acidic conditions used for (-)-7 provided not only the desired diols but also products of internal transacylation (oxazolidinone migration).
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 2949-2954
    • Williams, D.R.1    Sit, S.-Y.2
  • 60
    • 0028215543 scopus 로고
    • For recent references: (a)
    • For recent references: (a) Hattori, K.; Yamamoto, Y. Tetrahedron 1994, 50, 2785-2792.
    • (1994) Tetrahedron , vol.50 , pp. 2785-2792
    • Hattori, K.1    Yamamoto, Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.