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Volumn , Issue 12, 2003, Pages 1923-1926

Acyl Sulfonamide Catalysts for Glycosylation Reactions with Trichloroacetimidate Donors

Author keywords

Glycosylation; Hydrogen bond; Organocatalysis; Trichloroacetimidate

Indexed keywords

SULFONAMIDE; TRICHLOROACETIMIDIC ACID;

EID: 0142091318     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-41493     Document Type: Article
Times cited : (16)

References (26)
  • 4
    • 0242432417 scopus 로고    scopus 로고
    • For representative recent examples of reactions where H-bonds may play a key role as chiral Lewis acids, see: (a) Huang, Y.; Unni, A. K.; Thadani, A. N. ; Rawal, V. H. Nature (London) 2003, 424, 146. (b) Wenzel, A. G.; Jacobsen, E. N. J. Am. Chem. Soc. 2002, 124, 12964. (c) Vachal, P.; Jacobsen, E. N. J. Am. Chem. Soc. 2002, 124, 10012.
    • (2003) Nature (London) , vol.424 , pp. 146
    • Huang, Y.1    Unni, A.K.2    Thadani, A.N.3    Rawal, V.H.4
  • 5
    • 0037032312 scopus 로고    scopus 로고
    • For representative recent examples of reactions where H-bonds may play a key role as chiral Lewis acids, see: (a) Huang, Y.; Unni, A. K.; Thadani, A. N. ; Rawal, V. H. Nature (London) 2003, 424, 146. (b) Wenzel, A. G.; Jacobsen, E. N. J. Am. Chem. Soc. 2002, 124, 12964. (c) Vachal, P.; Jacobsen, E. N. J. Am. Chem. Soc. 2002, 124, 10012.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 12964
    • Wenzel, A.G.1    Jacobsen, E.N.2
  • 6
    • 0037189898 scopus 로고    scopus 로고
    • For representative recent examples of reactions where H-bonds may play a key role as chiral Lewis acids, see: (a) Huang, Y.; Unni, A. K.; Thadani, A. N. ; Rawal, V. H. Nature (London) 2003, 424, 146. (b) Wenzel, A. G.; Jacobsen, E. N. J. Am. Chem. Soc. 2002, 124, 12964. (c) Vachal, P.; Jacobsen, E. N. J. Am. Chem. Soc. 2002, 124, 10012.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 10012
    • Vachal, P.1    Jacobsen, E.N.2
  • 9
    • 0142101621 scopus 로고    scopus 로고
    • note
    • 5a
  • 13
    • 0142101620 scopus 로고    scopus 로고
    • note
    • Caution: picric acid is a potentially explosive compound when thoroughly dried (water content < 10%). We did not observe any difficulties of this type during these experiments.
  • 19
    • 0142070030 scopus 로고    scopus 로고
    • note
    • 11] requires m/z 369.0288. Found: 369.0282 (ESI+).
  • 20
    • 0142133290 scopus 로고    scopus 로고
    • note
    • All compounds gave satisfactory analytical data.
  • 21
    • 0142038093 scopus 로고    scopus 로고
    • note
    • 1H NMR spectroscopy.
  • 23
    • 0142133288 scopus 로고    scopus 로고
    • note
    • 6: C, 77.27; H, 8.03. Found: C, 77.00; H, 8.00.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.