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Volumn 53, Issue 17, 1997, Pages 6019-6026

Synthesis of 1-Deoxy-4-thio-D-ribose starting from thiophene-2-carboxylic acid

Author keywords

[No Author keywords available]

Indexed keywords

CARBOHYDRATE DERIVATIVE; THIOPHENE DERIVATIVE;

EID: 0030896616     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00290-1     Document Type: Article
Times cited : (18)

References (28)
  • 2
    • 84900403742 scopus 로고    scopus 로고
    • According to the IUPAC-Recommendations 1996 for the nomenclature of carbohydrates (Pure Appl. Chem., 1996, 68, 1919) the naming thia- and aza-sugars should be restricted to structures where carbon, not oxygen, is replaced by a heteroatom. On the other hand the structural resemblance of a carba-sugar (correct nomenclature according to these recommendations) with the corresponding sugar and its chalcogen analogues shows that the naming "thia"- and "aza"-sugar for these systems is appropriate to differentiate from thio- and amino-sugars, where the oxygen of a hydroxy group has been replaced by a sulfur or a nitrogen atom. See also Lehmann, J. Kohlenhydrate: Chemie und Biologie; 2.ed, Thieme: Stuttgart, New York, 1996, 130.
    • (1996) Pure Appl. Chem. , vol.68 , pp. 1919
  • 3
    • 0003667547 scopus 로고    scopus 로고
    • Thieme: Stuttgart, New York
    • According to the IUPAC-Recommendations 1996 for the nomenclature of carbohydrates (Pure Appl. Chem., 1996, 68, 1919) the naming thia- and aza-sugars should be restricted to structures where carbon, not oxygen, is replaced by a heteroatom. On the other hand the structural resemblance of a carba-sugar (correct nomenclature according to these recommendations) with the corresponding sugar and its chalcogen analogues shows that the naming "thia"- and "aza"-sugar for these systems is appropriate to differentiate from thio- and amino-sugars, where the oxygen of a hydroxy group has been replaced by a sulfur or a nitrogen atom. See also Lehmann, J. Kohlenhydrate: Chemie und Biologie; 2.ed, Thieme: Stuttgart, New York, 1996, 130.
    • (1996) Kohlenhydrate: Chemie und Biologie; 2.ed , pp. 130
    • Lehmann, J.1
  • 4
    • 0000412805 scopus 로고
    • Rowell, R.M.; Whistler, R.L. J. Org. Chem.. 1966, 31, 1514. Ermert, P.; Vasella, A. Helv. Chim. Acta 1993, 76, 2687; and references cited therein.
    • (1966) J. Org. Chem. , vol.31 , pp. 1514
    • Rowell, R.M.1    Whistler, R.L.2
  • 5
    • 0027442207 scopus 로고
    • and references cited therein
    • Rowell, R.M.; Whistler, R.L. J. Org. Chem.. 1966, 31, 1514. Ermert, P.; Vasella, A. Helv. Chim. Acta 1993, 76, 2687; and references cited therein.
    • (1993) Helv. Chim. Acta , vol.76 , pp. 2687
    • Ermert, P.1    Vasella, A.2
  • 13
    • 0343341552 scopus 로고    scopus 로고
    • note
    • The enzymatic resolution of the corresponding 2,5-dihydrofuran and 2,5-dihydropyrrole derivatives are under investigation.
  • 17
    • 85082559362 scopus 로고
    • Fatiadi, A.J. Synthesis, 1987, 85. Mochalin, V.B.; Kornilov, A.N.; Varpakhovskaya, I.S.; Vul'fson, A.N. Zh. Org. Khim. 1976, 12, 54.
    • (1987) Synthesis , pp. 85
    • Fatiadi, A.J.1
  • 21
    • 0000012312 scopus 로고
    • Morrison, J.D.(ed), Academic Press: Orlando
    • Bartlett, P.A. Asymmetric Synthesis, Morrison, J.D.(ed), Academic Press: Orlando, 1984, 3, 411.
    • (1984) Asymmetric Synthesis , vol.3 , pp. 411
    • Bartlett, P.A.1
  • 27
    • 0342906463 scopus 로고    scopus 로고
    • Purchased from Fluka
    • Purchased from Fluka.
  • 28
    • 0343341548 scopus 로고    scopus 로고
    • note
    • 10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.