메뉴 건너뛰기




Volumn 4, Issue 13, 2006, Pages 2549-2555

Synthesis of tetrahydroxy perhydroaza-azulenes: Tandem Johnson-Claisen rearrangement of d-glucose-derived allylic alcohols

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; ENZYME INHIBITION; ESTERS; GLUCOSE; HYDROGENATION;

EID: 33745432545     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b603545k     Document Type: Article
Times cited : (17)

References (36)
  • 32
    • 0034650428 scopus 로고    scopus 로고
    • 13C NMR spectra of compounds 11a, 13a, and 11b, 13b, in which theN-Cbz group is present, were insufficiently well-resolved to be able to confirm the 5-exo-tet-cyclization. This was due to isomerization by restricted rotation around CN - see:
    • A. Lubineau O. Gavard J. Alais D. Bonnaffe Tetradedron Lett. 2000 41 307 311
    • (2000) Tetradedron Lett. , vol.41 , pp. 307-311
    • Lubineau, A.1    Gavard, O.2    Alais, J.3    Bonnaffe, D.4
  • 33
    • 33745445632 scopus 로고
    • L. M. Jackman and S. Sternhell, Pergamon Press, Elmsford, NY, p. 361. An analogous observation has also been noticed - see:
    • Applications of NMR Spectroscopy in Organic Chemistry, ed., L. M. Jackman, and, S. Sternhell, Pergamon Press, Elmsford, NY, 1978, p. 361
    • (1978) Applications of NMR Spectroscopy in Organic Chemistry, Ed.
  • 34
    • 0026631232 scopus 로고
    • 1H NMR spectrum would be downfield, and appear as a double double doublet
    • Y. S. Denis T.-H. Chan J. Org. Chem. 1992 57 3078 3085
    • (1992) J. Org. Chem. , vol.57 , pp. 3078-3085
    • Denis, Y.S.1    Chan, T.-H.2
  • 35
    • 0037509698 scopus 로고
    • V. Ginsberg, Academic Press, Ginsburg, New York, vol. 28, part B, p. 702
    • Y.-T. Li, and S.-C. Li, in: Methods in Enzymology, ed., V. Ginsberg, Academic Press, Ginsburg, New York, vol. 28, part B, 1972, p. 702
    • (1972) Methods in Enzymology, Ed.
    • Li, Y.-T.1    Li, S.-C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.