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Volumn 16, Issue 14, 2014, Pages 3684-3687

Solvent effects in the nucleophilic substitutions of tetrahydropyran acetals promoted by trimethylsilyl trifluoromethanesulfonate: Trichloroethylene as solvent for stereoselective C - And O-glycosylations

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL DERIVATIVE; MESYLIC ACID DERIVATIVE; SOLVENT; TRICHLOROETHYLENE; TRIMETHYLSILYL DERIVATIVE; TRIMETHYLSILYL TRIFLUOROMETHANESULFONATE;

EID: 84904546896     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol501471c     Document Type: Article
Times cited : (34)

References (58)
  • 20
    • 0002917844 scopus 로고
    • Choice of solvent influences glycosylations even in reactions that do not involve triflates. See, for example: Eby, R.; Schuerch, C. Carbohydr. Res. 1974, 34, 79
    • (1974) Carbohydr. Res. , vol.34 , pp. 79
    • Eby, R.1    Schuerch, C.2
  • 25
    • 77956260481 scopus 로고    scopus 로고
    • Related reactions of bromofuranosides display similar behavior
    • Related reactions of bromofuranosides display similar behavior: Prévost, M.; St-Jean, O.; Guindon, Y. J. Am. Chem. Soc. 2010, 132, 12433
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 12433
    • Prévost, M.1    St-Jean, O.2    Guindon, Y.3
  • 45
    • 33745714287 scopus 로고    scopus 로고
    • A benzyloxy-substituted tetrahydropyran with a cyano group at the anomeric position adopted the diaxial conformation
    • A benzyloxy-substituted tetrahydropyran with a cyano group at the anomeric position adopted the diaxial conformation: Shenoy, S. R.; Smith, D. M.; Woerpel, K. A. J. Am. Chem. Soc. 2006, 128, 8671
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 8671
    • Shenoy, S.R.1    Smith, D.M.2    Woerpel, K.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.