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Volumn 78, Issue 14, 2013, Pages 7234-7248

Conformationally armed 3,6-tethered glycosyl donors: Synthesis, conformation, reactivity, and selectivity

Author keywords

[No Author keywords available]

Indexed keywords

ANOMERIC PAIRS; ELECTRONIC CHARACTERISTICS; GLUCOPYRANOSIDE; GLYCOSYL DONORS; HIGH YIELD; THIOGLYCOSIDES; THIOPHENYL;

EID: 84880542187     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo4012464     Document Type: Article
Times cited : (53)

References (64)
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    • The use of axial-rich glycosyl donors have recently been reviewed: Yamada, H. Trends Glycosci. Glycotechnol. 2011, 23, 122-133
    • (2011) Trends Glycosci. Glycotechnol. , vol.23 , pp. 122-133
    • Yamada, H.1
  • 47
    • 20444483055 scopus 로고
    • The angles were calculated using the program available at according to
    • The angles were calculated using the program available at http://www.stenutz.eu/conf/haasnoot.php according to Haasnoot, C. A. G.; DeLeeuw, F. A. A. M.; Altona, C. Tetrahedron 1980, 36, 2783-2792
    • (1980) Tetrahedron , vol.36 , pp. 2783-2792
    • Haasnoot, C.A.G.1    Deleeuw, F.A.A.M.2    Altona, C.3
  • 49
    • 0034733128 scopus 로고    scopus 로고
    • The Perlin effect might be less reliable when having thioglycosides
    • The Perlin effect might be less reliable when having thioglycosides: Alabugin, I. V. J. Org. Chem. 2000, 65, 3910-3919
    • (2000) J. Org. Chem. , vol.65 , pp. 3910-3919
    • Alabugin, I.V.1
  • 55
    • 0039479242 scopus 로고
    • Similar explanation has been presented by Miljkovic et al. to explain the greater rate of acetolysis of α-anomers
    • Similar explanation has been presented by Miljkovic et al. to explain the greater rate of acetolysis of α-anomers: Miljkovic, M.; Habash-Marino, M. J. Org. Chem. 1983, 48, 855-860
    • (1983) J. Org. Chem. , vol.48 , pp. 855-860
    • Miljkovic, M.1    Habash-Marino, M.2
  • 63
    • 47249092878 scopus 로고    scopus 로고
    • The steric bulk of a 4,6-di- O -di- tert -butylsilylene bridge has been used in α-selective galactosylations. Reviewed in
    • The steric bulk of a 4,6-di- O -di- tert -butylsilylene bridge has been used in α-selective galactosylations. Reviewed in: Imamura, A.; Ando, H.; Ishida, H.; Kiso, M. Curr. Org. Chem. 2008, 12, 675-689
    • (2008) Curr. Org. Chem. , vol.12 , pp. 675-689
    • Imamura, A.1    Ando, H.2    Ishida, H.3    Kiso, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.