메뉴 건너뛰기




Volumn 59, Issue 24, 2003, Pages 4249-4259

The cycloaddition way to novel deoxy disaccharide analogs

Author keywords

Cycloaddition; Desulfurization; Glycosyl transfer; Tetronic acid

Indexed keywords

CARBOHYDRATE DERIVATIVE; CARBON; DISACCHARIDE; HETEROCYCLIC COMPOUND; LACTONE DERIVATIVE; SULFIDE;

EID: 0038361115     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)00654-9     Document Type: Article
Times cited : (13)

References (35)
  • 1
    • 0033518559 scopus 로고    scopus 로고
    • (a) Zhang Z., Ollmann I.R., Ye X.-S., Wischnat R., Baasov T., Wong C.-H. J. Am. Chem. Soc. 121:1999;734-753 (b) Barresi F., Hindsgaul O. J. Carbohydr. Chem. 14:1995;1043-1087 (c) Ernst B., Hart G.W., Sinay P. Chemical Syntheses of Glycosides and Glycomimetics. Chemical Syntheses of Glycosides and Glycomimetics. Vol. 1:2000;Wiley-VCH, Weinheim.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 734-753
    • Zhang, Z.1    Ollmann, I.R.2    Ye, X.-S.3    Wischnat, R.4    Baasov, T.5    Wong, C.-H.6
  • 2
    • 0000387792 scopus 로고
    • (a) Zhang Z., Ollmann I.R., Ye X.-S., Wischnat R., Baasov T., Wong C.-H. J. Am. Chem. Soc. 121:1999;734-753 (b) Barresi F., Hindsgaul O. J. Carbohydr. Chem. 14:1995;1043-1087 (c) Ernst B., Hart G.W., Sinay P. Chemical Syntheses of Glycosides and Glycomimetics. Chemical Syntheses of Glycosides and Glycomimetics. Vol. 1:2000;Wiley-VCH, Weinheim.
    • (1995) J. Carbohydr. Chem. , vol.14 , pp. 1043-1087
    • Barresi, F.1    Hindsgaul, O.2
  • 3
    • 0033518559 scopus 로고    scopus 로고
    • B. Ernst, G.W. Hart, & P. Sinay. Weinheim: Wiley-VCH
    • (a) Zhang Z., Ollmann I.R., Ye X.-S., Wischnat R., Baasov T., Wong C.-H. J. Am. Chem. Soc. 121:1999;734-753 (b) Barresi F., Hindsgaul O. J. Carbohydr. Chem. 14:1995;1043-1087 (c) Ernst B., Hart G.W., Sinay P. Chemical Syntheses of Glycosides and Glycomimetics. Chemical Syntheses of Glycosides and Glycomimetics. Vol. 1:2000;Wiley-VCH, Weinheim.
    • (2000) Chemical Syntheses of Glycosides and Glycomimetics , vol.1
  • 5
    • 0034693085 scopus 로고    scopus 로고
    • (a) Marzabadi C.H., Franck R.W. Tetrahedron. 56:2000;8385-8417 (b) Veyrieres A. Ref. 1(c), Chapter 15, 367-406.
    • (2000) Tetrahedron , vol.56 , pp. 8385-8417
    • Marzabadi, C.H.1    Franck, R.W.2
  • 6
    • 0034693085 scopus 로고    scopus 로고
    • Ref. 1(c), Chapter 15, 367-406
    • (a) Marzabadi C.H., Franck R.W. Tetrahedron. 56:2000;8385-8417 (b) Veyrieres A. Ref. 1(c), Chapter 15, 367-406.
    • Veyrieres, A.1
  • 7
    • 0034693085 scopus 로고    scopus 로고
    • (a) Marzabadi C.H., Franck R.W. Tetrahedron. 56:2000;8385-8417 (b) Veyrieres A. Ref. 1(c), Chapter 15, 367-406.
  • 9
    • 0033553134 scopus 로고    scopus 로고
    • (a) Roush W.R., Bennett C.E. J. Am. Chem. Soc. 121:1999;3541-3542 (b) Roush W.R., Bennett C.E. J. Am. Chem. Soc. 122:2000;6124-6125.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 3541-3542
    • Roush, W.R.1    Bennett, C.E.2
  • 10
    • 0034725372 scopus 로고    scopus 로고
    • (a) Roush W.R., Bennett C.E. J. Am. Chem. Soc. 121:1999;3541-3542 (b) Roush W.R., Bennett C.E. J. Am. Chem. Soc. 122:2000;6124-6125.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 6124-6125
    • Roush, W.R.1    Bennett, C.E.2
  • 12
    • 0024444843 scopus 로고
    • (a) Yin H., Franck R.W., Chen S.-, Quigley G.J., Todaro L. J. Org. Chem. 57:1992;644-651 (b) Gupta R.B., Franck R.W. J. Am. Chem. Soc. 111:1989;7668-7669.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 7668-7669
    • Gupta, R.B.1    Franck, R.W.2
  • 15
    • 0037151559 scopus 로고    scopus 로고
    • For a unique glycal functionalization via a non-cycloaddition route: (a) Liu J., Gin D.Y. J. Am. Chem. Soc. 124:2002;9789-9797 (b) Honda E., Gin D.Y. J. Am. Chem. Soc. 124:2002;7343-7352.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 9789-9797
    • Liu, J.1    Gin, D.Y.2
  • 16
    • 0037178051 scopus 로고    scopus 로고
    • For a unique glycal functionalization via a non-cycloaddition route: (a)
    • For a unique glycal functionalization via a non-cycloaddition route: (a) Liu J., Gin D.Y. J. Am. Chem. Soc. 124:2002;9789-9797 (b) Honda E., Gin D.Y. J. Am. Chem. Soc. 124:2002;7343-7352.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 7343-7352
    • Honda, E.1    Gin, D.Y.2
  • 19
    • 0036132394 scopus 로고    scopus 로고
    • For two recent papers describing this approach (a)
    • For two recent papers describing this approach (a) Bartolozzi A., Capozzi G., Falciani C., Menichetti S., Nativi C., Bacialli A.P. J. Org. Chem. 64:1999;6490-6494 (b) Marzabadi C.H., Franck R.W., Schinazi R.F. Bioorg. Med. Chem. 10:2002;273-281.
    • (2002) Bioorg. Med. Chem. , vol.10 , pp. 273-281
    • Marzabadi, C.H.1    Franck, R.W.2    Schinazi, R.F.3
  • 29
    • 0037985085 scopus 로고    scopus 로고
    • (a) Bombala M.U., Ley S.V. J. Chem. Soc. Perkin Trans. 1. 1979;3013-3016 (b) Win W.W., Franck R.W. J. Org. Chem. 4510:1997;4512.
    • (1997) J. Org. Chem. , vol.4510 , pp. 4512
    • Win, W.W.1    Franck, R.W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.