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Volumn 73, Issue 11, 2008, Pages 4305-4308

Introduction of vinyl and hydroxymethyl functionalities at C-4 of glucose-derived substrates: Synthesis of spirocyclic, bicyclic, and tricyclic nucleosides

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; CHEMICAL REACTIONS; DIFFERENCE EQUATIONS; GLUCOSE; METHANOL; SUBSTRATES;

EID: 44949083587     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo8002826     Document Type: Article
Times cited : (26)

References (23)
  • 9
    • 1142281160 scopus 로고    scopus 로고
    • and references cited therein
    • (d) Paquette, L. A. Aust. J. Chem. 2004, 57, 7-17, and references cited therein.
    • (2004) Aust. J. Chem , vol.57 , pp. 7-17
    • Paquette, L.A.1
  • 17
    • 44949150519 scopus 로고    scopus 로고
    • Hydroboration of 10 with 9-BBN was not successful possibly due to the steric hindrance offered to the approach of the reagent by the bulky tert-butyldimethylsilyloxymethyl functionality at C-4′.
    • Hydroboration of 10 with 9-BBN was not successful possibly due to the steric hindrance offered to the approach of the reagent by the bulky tert-butyldimethylsilyloxymethyl functionality at C-4′.
  • 18
    • 44949163966 scopus 로고    scopus 로고
    • ORTEP diagram(s) are given in the Supporting Information
    • ORTEP diagram(s) are given in the Supporting Information.
  • 23
    • 44949097689 scopus 로고    scopus 로고
    • 14b of 27 unexpectedly removed the uracil moiety along with removal of benzyl groups.
    • 14b of 27 unexpectedly removed the uracil moiety along with removal of benzyl groups.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.