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Volumn 133, Issue 5, 2011, Pages 1597-1602

Encouraging progress in the ω-aspartylation of complex oligosaccharides as a general route to β-N-linked glycopolypeptides

Author keywords

[No Author keywords available]

Indexed keywords

ASPARTATES; COMPLEX COMPONENTS; N-LINKED; OXIDATIVE COUPLINGS;

EID: 79551711838     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja110115a     Document Type: Article
Times cited : (57)

References (38)
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    • For a recent review, see
    • Kan, C.; Danishefsky, S. J. Tetrahedron 2009, 65, 9047 For a recent review, see
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    • Kan, C.1    Danishefsky, S.J.2
  • 14
    • 0025085939 scopus 로고
    • For an excellent catalog of other aspartylation methods, see ref 5
    • For an excellent catalog of other aspartylation methods, see ref 5 Anisfeld, S. T.; Lansbury, P. T. J. Org. Chem. 1990, 55, 5560
    • (1990) J. Org. Chem. , vol.55 , pp. 5560
    • Anisfeld, S.T.1    Lansbury, P.T.2
  • 19
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    • references to the original isonitrile literature therein
    • and references to the original isonitrile literature therein Li, X.; Yuan, Y.; Kan, C.; Danishefsky, S. J. J. Am. Chem. Soc. 2008, 130, 13225
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 13225
    • Li, X.1    Yuan, Y.2    Kan, C.3    Danishefsky, S.J.4
  • 24
    • 79551709040 scopus 로고    scopus 로고
    • Of course, the resultant thio-formamide could be recycled to the amine precursor of the isonitrile at the manufacture level.
    • Of course, the resultant thio-formamide could be recycled to the amine precursor of the isonitrile at the manufacture level.
  • 25
    • 79551717679 scopus 로고    scopus 로고
    • We also note that through the use of hindered isonitriles, the S→N rearrangement can be suppressed to the point where it is negligible.
    • We also note that through the use of hindered isonitriles, the S→N rearrangement can be suppressed to the point where it is negligible.
  • 30
    • 70450192533 scopus 로고    scopus 로고
    • For the synthesis of hexasaccharide 15, see the Supporting Information
    • For the synthesis of hexasaccharide 15, see the Supporting Information Wang, P.; Zhu, J.; Yuan, Y.; Danishefsky, S. J. J. Am. Chem. Soc. 2009, 131, 16669
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 16669
    • Wang, P.1    Zhu, J.2    Yuan, Y.3    Danishefsky, S.J.4
  • 34
    • 0000862045 scopus 로고
    • An earlier perception of the oxidative possibility, also in a stoichiometric sense, appeared in 1952. See
    • Sheehan, J. C.; Johnson, D. A. J. Am. Chem. Soc. 1952, 74, 4726 An earlier perception of the oxidative possibility, also in a stoichiometric sense, appeared in 1952. See
    • (1952) J. Am. Chem. Soc. , vol.74 , pp. 4726
    • Sheehan, J.C.1    Johnson, D.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.