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Volumn 3, Issue 10, 2005, Pages 1893-1904

Deprotonation-electrophile trapping of terminal epoxides

Author keywords

[No Author keywords available]

Indexed keywords

ACIDITY; COMPLEXATION; NEGATIVE IONS; NITROGEN COMPOUNDS; REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 19944414392     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b502888d     Document Type: Article
Times cited : (22)

References (44)
  • 1
    • 0002960755 scopus 로고    scopus 로고
    • ed. A. R. Katritzky, C. W. Rees and E. F. V. Scriven, Pergamon, Oxford
    • I. Erden, in Comprehensive Heterocyclic Chemistry II, vol. 1A, ed. A. R. Katritzky, C. W. Rees and E. F. V. Scriven, Pergamon, Oxford, 1996, pp. 97.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.1 A , pp. 97
    • Erden, I.1
  • 2
  • 27
    • 0033215353 scopus 로고    scopus 로고
    • Table 2, entry 7
    • (b) J. D. Warren and Y. Shi, J. Org. Chem., 1999, 64, 7675 (Table 2, entry 7).
    • (1999) J. Org. Chem. , vol.64 , pp. 7675
    • Warren, J.D.1    Shi, Y.2
  • 39
    • 19944385877 scopus 로고    scopus 로고
    • note
    • Epoxides 1 in Table 4 were either commercially available, prepared as described previously (ref. 11, above) or prepared according to: (a) 1,2-epoxy-5-(5,5-dimethyl-[1,3]dioxanyl)hexane was prepared in two steps from 5-hexen-2-one (entry 8); (b) cyclohexyl oxirane was prepared according to ref. 11d, above.
  • 40
    • 19944385529 scopus 로고    scopus 로고
    • note
    • Tentative stereochemical assignments for epoxy alcohol diastereoisomers 14 were made by comparison of NMR spectral data with those of structurally similar compounds in the following reports: (a) ref. 12 above;
  • 43
    • 19944398699 scopus 로고    scopus 로고
    • note
    • 2F) has so far been unsuccessful.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.