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Volumn 3, Issue 1, 2013, Pages 57-60

Gold-catalyzed synthesis of 2-deoxy glycosides using S-But-3-ynyl thioglycoside donors

Author keywords

2 deoxy glycosides; Alkyne; Glycosylation; Gold; Homogeneous catalysis

Indexed keywords

ALKYNE; HOMOGENEOUS CATALYSIS; OPTIMAL CONDITIONS; STEREOSELECTIVE SYNTHESIS; TERTIARY ALCOHOLS; THIOGLYCOSIDES;

EID: 84874042769     PISSN: 21555435     EISSN: None     Source Type: Journal    
DOI: 10.1021/cs300670k     Document Type: Article
Times cited : (76)

References (46)
  • 38
    • 84865519692 scopus 로고    scopus 로고
    • During the preparation of our manuscript, Yu and co-workers reported the use of ortho-alkynylphenyl thioglycosides as a new type of glycosylation donors under the catalysis of Au(I) complexes. See: Yang, F.; Wang, Q.; Yu, B. Tetrahedron Lett. 2012, 53, 5231-5234.
    • (2012) Tetrahedron Lett. , vol.53 , pp. 5231-5234
    • Yang, F.1    Wang, Q.2    Yu, B.3
  • 39
    • 84862858560 scopus 로고    scopus 로고
    • Recently, Hotha and co-workers reported Au(III)-catalyzed Oglycosylations employing "armed" substituted propargyl glycoside donors at ambient temperature. See: Kayastha, A. K.; Hotha, S. Chem. Commun. 2012, 48, 7161-7163.
    • (2012) Chem. Commun. , vol.48 , pp. 7161-7163
    • Kayastha, A.K.1    Hotha, S.2
  • 40
    • 33746653349 scopus 로고    scopus 로고
    • Previously, Hotha and co-workers disclosed Au(III)-catalyzed O-glycosylations employing "armed" propargyl glycoside donors at elevated temperature. See: Hotha, S.; Kashyap, S. J. Am. Chem. Soc. 2006, 128, 9620-9621.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 9620-9621
    • Hotha, S.1    Kashyap, S.2
  • 41
    • 0031795583 scopus 로고    scopus 로고
    • Previously, Kunz and co-workers reported that (S)-pent-4-enyl thioglycosides can be activated by a stoichiometric amount of NIS/TfOH. See: Leuck, M.; Kunz, H. Carbohydr. Res. 1998, 312, 33-44.
    • (1998) Carbohydr. Res. , vol.312 , pp. 33-44
    • Leuck, M.1    Kunz, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.