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Volumn 8, Issue 17, 1997, Pages 2839-2876

O-Glycosyl α-amino acids as building blocks for glycopeptide synthesis

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOPEPTIDE; GLYCOPROTEIN; MUCIN;

EID: 0030845782     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(97)00326-1     Document Type: Article
Times cited : (90)

References (292)
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    • TR 388
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    • (1996) Tetrahedron , vol.52 , pp. 1095-1121
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  • 29
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    • Other groups previously used are: Dnpeoc, Peoc, Pyoc, MPc, Aloc, Noc. Groups such as Noc, Aloc and Allyl groups will be very useful for the selective access to particular groups in side chains of assembled peptides
    • Other groups previously used are: Dnpeoc, Peoc, Pyoc, MPc, Aloc, Noc. Groups such as Noc, Aloc and Allyl groups will be very useful for the selective access to particular groups in side chains of assembled peptides.
  • 38
    • 0343877575 scopus 로고    scopus 로고
    • note
    • For semipermanent C-terminal protection tert-butyl, benzyl, methyl, Dim (1,3-dithian-2-yl methyl), 2-haloethyl, and allyl esters have been used. Phenacyl and Maq (9,10-anthraquino-2-yl methyl) esters which can be removed by treatment with Zn in AcOH and sodium dithionite, respectively, have also been used.
  • 59
    • 0021141716 scopus 로고
    • a) G.F. Springer, Science 1984, 224, 1198-1206;
    • (1984) Science , vol.224 , pp. 1198-1206
    • Springer, G.F.1
  • 98
  • 142
    • 0000499264 scopus 로고
    • Synthetic oligosaccharides
    • Kóvac, P. Ed., American Chemical Society, Washington DC
    • Y. Nakahara, H. Iijima, T. Ogawa, in Synthetic Oligosaccharides Kóvac, P. Ed., ACS Symposium series 560, American Chemical Society, Washington DC 1994, pp 249-266.
    • (1994) ACS Symposium Series 560 , pp. 249-266
    • Nakahara, Y.1    Iijima, H.2    Ogawa, T.3
  • 153
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    • a) K. Suzuki, H. Maeta, T. Matsumoto, G. Tsuchihashi, Tetrahedron Lett. 1988, 29, 3567-3570, ibid. 3571-3574;
    • Tetrahedron Lett. , pp. 3571-3574
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    • 0001937994 scopus 로고
    • Synthetic Methods for Carbohydrates
    • El Khadem, H.S., Ed; Washington DC
    • a) R.U. Lemieux, T. Takeda, B.Y. Chung, In Synthetic Methods for Carbohydrates; El Khadem, H.S., Ed; Am. Chem. Soc. Symp. Ser., Washington DC, 1976, 39, 90-115;
    • (1976) Am. Chem. Soc. Symp. Ser. , vol.39 , pp. 90-115
    • Lemieux, R.U.1    Takeda, T.2    Chung, B.Y.3
  • 220
    • 33748627212 scopus 로고    scopus 로고
    • a) This kind of protecting group has been very recently used in the synthesis of O-GlcNAc Ser/Thr building blocks, U. K. Saha, R. R. Schmidt, J. Chem. Soc. Perkins Trans. I, 1997, 1855-1860.
    • (1997) J. Chem. Soc. Perkins Trans. I , pp. 1855-1860
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    • A. Gottschalk (Ed.), Elsevier, N.Y.
    • a) U. Lindahl, L. Rodén, in A. Gottschalk (Ed.), Glycoproteins, Elsevier, N.Y., 1972, pp. 491-517;
    • (1972) Glycoproteins , pp. 491-517
    • Lindahl, U.1    Rodén, L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.