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Volumn 338, Issue 2, 2003, Pages 123-132

Conformational evaluation of some 4-deoxyhex-4-enopyranose derivatives and their use in the preparation of a previously undescribed class of 3-thio-L-sorbopyranosides and their 6-C-methoxy analogues

Author keywords

3 Thio L sorbopyranosides; 4 Deoxyhex 4 enopyranose derivatives; Conformations; Cycloadditions; Oxothiones

Indexed keywords

CONFORMATIONS; STEREOCHEMISTRY; UNSATURATED COMPOUNDS;

EID: 0347297123     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0008-6215(02)00431-7     Document Type: Article
Times cited : (4)

References (34)
  • 22
    • 0012390524 scopus 로고
    • For hex-3-enopyranosides, see: (a) Achmatowicz, O.; Banaszek, A; Chmielewski, M; Zamojski, A. Carbohydr. Res. 1974, 36, 13-22; For hex-2-enopyranose (-osides), see: (b) Thiem, J.; Schwentner, J.; Schüttpelz, E.; Kopf, J. Chem. Ber. 1979, 112, 1023-1034; (c) Angerbauer, R.; Schmidt, R. R. Carbohydr. Res. 1981, 89, 193-201.
    • (1974) Carbohydr. Res. , vol.36 , pp. 13-22
    • Achmatowicz, O.1    Banaszek, A.2    Chmielewski, M.3    Zamojski, A.4
  • 23
    • 0001694695 scopus 로고
    • For hex-3-enopyranosides, see: (a) Achmatowicz, O.; Banaszek, A; Chmielewski, M; Zamojski, A. Carbohydr. Res. 1974, 36, 13-22; For hex-2-enopyranose (-osides), see: (b) Thiem, J.; Schwentner, J.; Schüttpelz, E.; Kopf, J. Chem. Ber. 1979, 112, 1023-1034; (c) Angerbauer, R.; Schmidt, R. R. Carbohydr. Res. 1981, 89, 193-201.
    • (1979) Chem. Ber. , vol.112 , pp. 1023-1034
    • Thiem, J.1    Schwentner, J.2    Schüttpelz, E.3    Kopf, J.4
  • 24
    • 0000667781 scopus 로고
    • For hex-3-enopyranosides, see: (a) Achmatowicz, O.; Banaszek, A; Chmielewski, M; Zamojski, A. Carbohydr. Res. 1974, 36, 13-22; For hex-2-enopyranose (-osides), see: (b) Thiem, J.; Schwentner, J.; Schüttpelz, E.; Kopf, J. Chem. Ber. 1979, 112, 1023-1034; (c) Angerbauer, R.; Schmidt, R. R. Carbohydr. Res. 1981, 89, 193-201.
    • (1981) Carbohydr. Res. , vol.89 , pp. 193-201
    • Angerbauer, R.1    Schmidt, R.R.2
  • 29
    • 0346163299 scopus 로고    scopus 로고
    • Surprisingly, 14 was the only ortho-thioquinone which cycloadded with compounds 1, 2 and 6
    • Surprisingly, 14 was the only ortho-thioquinone which cycloadded with compounds 1, 2 and 6.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.