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Volumn 18, Issue 2, 1999, Pages 191-207

Preparation of 2,5-anhydrohexitols (part II). Intramolecular nucleophilic substitution of cyclic sulfates

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Indexed keywords


EID: 0033472378     PISSN: 07328303     EISSN: None     Source Type: Journal    
DOI: 10.1080/07328309908543990     Document Type: Article
Times cited : (8)

References (32)
  • 3
    • 0009047278 scopus 로고
    • PhD Thesis, Leiden University
    • P.A.M. van der Klein, PhD Thesis, Leiden University, 1992.
    • (1992)
    • Van Der Klein, P.A.M.1
  • 23
    • 85033963168 scopus 로고    scopus 로고
    • note
    • Compounds 5 and 25 did not dissolve in pure MeOH.
  • 24
    • 85033964717 scopus 로고    scopus 로고
    • note
    • Chemical shifts of the ring methine carbons are also highly indicative of ring size, i.e. THF carbon atoms are generally found 5-15 ppm downfield from those in 6-membered rings.
  • 27
    • 0009073551 scopus 로고
    • See also reference 15
    • Hydrogenation of 11 gave 1,5-anhydro-L-gulitol. R.K. Ness, H.G. Fletcher Jr., J. Am. Chem. Soc., 75, 2619 (1953). See also reference 15.
    • (1953) J. Am. Chem. Soc. , vol.75 , pp. 2619
    • Ness, R.K.1    Fletcher H.G., Jr.2
  • 28
    • 0001501630 scopus 로고
    • See also reference 15
    • Hydrogenation of 20 and 29 gave 1,5-anhydro-D-talitol and 1,5-anhydro-D-iditol, respectively. D.A. Rosenfeld, N.K. Richtmyer, C.S. Hudson, J. Am. Chem. Soc., 70, 2201 (1948). See also reference 15.
    • (1948) J. Am. Chem. Soc. , vol.70 , pp. 2201
    • Rosenfeld, D.A.1    Richtmyer, N.K.2    Hudson, C.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.