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Volumn , Issue 2, 2003, Pages 276-277

A novel diastereoselective route to α-hydroxyalkyl dihydropyrans using a hetero Diels-Alder/allylboration sequence

Author keywords

[No Author keywords available]

Indexed keywords

BORIC ACID; PYRAN DERIVATIVE;

EID: 0037243856     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b208572k     Document Type: Article
Times cited : (34)

References (23)
  • 1
    • 0001399971 scopus 로고
    • For selected reviews, see: R. D. Norcross and I. Paterson, Chem. Rev., 1995, 95, 2041; D. J. Faulkner, Nat. Prod. Rep., 1997, 14, 259.
    • (1995) Chem. Rev. , vol.95 , pp. 2041
    • Norcross, R.D.1    Paterson, I.2
  • 2
    • 0030841236 scopus 로고    scopus 로고
    • For selected reviews, see: R. D. Norcross and I. Paterson, Chem. Rev., 1995, 95, 2041; D. J. Faulkner, Nat. Prod. Rep., 1997, 14, 259.
    • (1997) Nat. Prod. Rep. , vol.14 , pp. 259
    • Faulkner, D.J.1
  • 8
    • 0000884707 scopus 로고
    • ed. B. M. Trost and I. Fleming, Pergamon Press
    • (b) D. L. Boger in Comprehensive Organic Chemistry, ed. B. M. Trost and I. Fleming, Pergamon Press, 1987, vol. 5, p. 451;
    • (1987) Comprehensive Organic Chemistry , vol.5 , pp. 451
    • Boger, D.L.1
  • 18
    • 0012667762 scopus 로고    scopus 로고
    • note
    • When freshly distilled acetaldehyde is used, the product 2 is not obtained. The cleavage of the diethyl acetal is probably due to the presence of small quantities of acetic acid in acetaldehyde.
  • 20
    • 0012747714 scopus 로고    scopus 로고
    • note
    • We did not carry out other tests at higher temperatures because the heterodiene 1 is prone to thermal decomposition.
  • 22
    • 0012738595 scopus 로고    scopus 로고
    • note
    • All new compounds were completely characterized (1H NMR, 13C NMR, elemental analysis or HRMS).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.