메뉴 건너뛰기




Volumn 16, Issue 39, 2010, Pages 11915-11925

Internally protected amino sugar equivalents from enantiopure 1,2-oxazines: Synthesis of variably configured carbohydrates with C-branched amino sugar units

Author keywords

allenes; amino sugars; carbohydrates; glycosidation; rearrangement

Indexed keywords

AGLYCONS; ALLENES; AMINO SUGAR; BUILDING BLOCKES; DEPROTECTION; ENANTIOPURE; GLYCOSIDATIONS; GLYCOSYL ACCEPTORS; GLYCOSYL DONORS; GLYCOSYLATED; L-SERINE; LEWIS ACID; MEDICINAL CHEMISTRY; METHYL GLYCOSIDES; NATURAL PRODUCTS; PHENYLTHIO; POTENTIAL APPLICATIONS; REARRANGEMENT; STEREODIVERGENT SYNTHESIS;

EID: 78249265314     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201001060     Document Type: Article
Times cited : (20)

References (67)
  • 1
    • 84956473972 scopus 로고    scopus 로고
    • (Eds.: B. Ernst, G. W. Hart, P. Sinaÿ), WILEY-VCH, Weinheim.
    • Carbohydrates in Chemistry and Biology (Eds.:, B. Ernst, G. W. Hart, P. Sinaÿ,), WILEY-VCH, Weinheim, 2000.
    • (2000) Carbohydrates in Chemistry and Biology
  • 3
    • 78249267055 scopus 로고    scopus 로고
    • Reviews
    • Reviews
  • 11
    • 78249238011 scopus 로고    scopus 로고
    • Reviews
    • Reviews
  • 14
    • 33645788031 scopus 로고    scopus 로고
    • in (Eds.: D. E. Levy, P. Fügedi), Taylor and Francis, Boca Raton,. For selected examples of organocatalytic de novo syntheses of carbohydrates, see
    • P. Vogel, in The Organic Chemistry of Sugars (Eds.:, D. E. Levy, P. Fügedi,), Taylor and Francis, Boca Raton, 2006, pp. 629 - 728. For selected examples of organocatalytic de novo syntheses of carbohydrates, see
    • (2006) The Organic Chemistry of Sugars , pp. 629-728
    • Vogel, P.1
  • 17
    • 15444380834 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 1210 - 1212.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 1210-1212
  • 22
    • 84914202563 scopus 로고    scopus 로고
    • Freie Universität Berlin (Germany)
    • V. Dekaris, Dissertation, Freie Universität Berlin (Germany), 2009
    • (2009) Dissertation
    • Dekaris, V.1
  • 25
    • 70349784899 scopus 로고    scopus 로고
    • 3169. For the synthesis of related aminopyrans without an anomeric center leading to carbohydrate mimetics, see
    • Angew. Chem. Int. Ed. 2009, 48, 3165 - 3169. For the synthesis of related aminopyrans without an anomeric center leading to carbohydrate mimetics, see
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 3165
  • 27
    • 25844449046 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 6227 - 6231
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 6227-6231
  • 35
    • 78249268643 scopus 로고    scopus 로고
    • The corresponding anti-1,2-oxazines can not lead to similar rearrangement products (see ref. [14])
    • The corresponding anti-1,2-oxazines can not lead to similar rearrangement products (see ref. [14]).
  • 37
    • 84869113703 scopus 로고    scopus 로고
    • Freie Universität Berlin (Germany)
    • M. Roskamp, Dissertation, Freie Universität Berlin (Germany), 2010.
    • (2010) Dissertation
    • Roskamp, M.1
  • 41
    • 0025125757 scopus 로고
    • 1334. For a review on recent achievements in glycoside-bond formation, see
    • G. H. Veeneman, S. H. van Leeuwen, J. H. van Boom, Tetrahedron Lett. 1990, 31, 1331 - 1334. For a review on recent achievements in glycoside-bond formation, see
    • (1990) Tetrahedron Lett. , vol.31 , pp. 1331
    • Veeneman, G.H.1    Van Leeuwen, S.H.2    Van Boom, J.H.3
  • 43
    • 61849111654 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 1900 - 1934.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 1900-1934
  • 44
    • 78249270559 scopus 로고    scopus 로고
    • The configurations of compounds 32 - 34 have been assigned by comparison of their NMR data with the corresponding phenyl-substituted derivatives (see ref. [9b])
    • The configurations of compounds 32 - 34 have been assigned by comparison of their NMR data with the corresponding phenyl-substituted derivatives (see ref. [9b]).
  • 46
    • 26844456596 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 6315 - 6318.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 6315-6318
  • 47
    • 78249270249 scopus 로고    scopus 로고
    • For selected examples of the de novo synthesis of di- and trisaccharides by using palladium-catalyzed reactions, see
    • For selected examples of the de novo synthesis of di- and trisaccharides by using palladium-catalyzed reactions, see
  • 55
    • 78249263041 scopus 로고    scopus 로고
    • For examples of bivalent aminoglycoside mimetics, see
    • For examples of bivalent aminoglycoside mimetics, see
  • 58
    • 4143076674 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 1562 - 1566.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 1562-1566
  • 59
    • 78249243554 scopus 로고    scopus 로고
    • 2, see
    • 2, see
  • 64
    • 78249262734 scopus 로고    scopus 로고
    • (Ed.: V. Wittmann), Springer, Berlin.
    • Glycopeptides and Glycoproteins (Ed.:, V. Wittmann,), Springer, Berlin, 2007.
    • (2007) Glycopeptides and Glycoproteins


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.