메뉴 건너뛰기




Volumn 59, Issue 39, 2003, Pages 7803-7810

High regioselectivity in the heterocyclization of β-oxonitriles to 4-oxothiazolidines: X-ray structure proof

Author keywords

Cyclisation; Regiospecificity; Thiazolidines

Indexed keywords

ALKENE DERIVATIVE; ETHYL 5 ETHOXYCARBONYLMETHYL 4 OXOTHIAZOLIDIN 2 YLIDENE ETHANOATE; NITRILE; THIAZOLIDINE DERIVATIVE; THIOMALIC ACID; UNCLASSIFIED DRUG;

EID: 0041833701     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)01146-3     Document Type: Article
Times cited : (39)

References (29)
  • 13
    • 0001485030 scopus 로고
    • New York: Academic. pp 83-111. A.R. Katritzky, Rees C.W. Oxford: Pergamon. Chapter 19
    • (c) Metzger J.V. Katritzky A.R., Rees C.W. Comprehensive Heterocyclic Chemistry. Vol. 6:1984;236-330 Pergamon, Oxford. Chapter 19.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.6 , pp. 236-330
    • Metzger, J.V.1
  • 25
    • 0001225069 scopus 로고    scopus 로고
    • 3a-d, affording under mild experimental conditions vinyl bromides in good yields, reflects the enaminic susceptibility toward electrophiles, for additional examples see (a)
    • Regioselective α-bromination of (Z)-5-substituted-2-alkylidene-4-oxothiazolidine derivatives 3a-d, affording under mild experimental conditions vinyl bromides in good yields, reflects the enaminic susceptibility toward electrophiles, for additional examples see (a) Kordik C.P., Reitz A.B. J. Org. Chem. 61:1996;5644-5645 (b) Stork G., Brizzolara A., Landesman H., Szmuszkovitz J., Terrell R. J. Am. Chem. Soc. 85:1963;207-222 (c) Tokumitsu T., Hayashi T. J. Org. Chem. 50:1985;1547-1550.
    • (1996) J. Org. Chem. , vol.61 , pp. 5644-5645
    • Kordik, C.P.1    Reitz, A.B.2
  • 26
    • 33947482604 scopus 로고
    • Regioselective α-bromination of (Z)-5-substituted-2-alkylidene-4-oxothiazolidine derivatives 3a-d, affording under mild experimental conditions vinyl bromides in good yields, reflects the enaminic susceptibility toward electrophiles, for additional examples see (a) Kordik C.P., Reitz A.B. J. Org. Chem. 61:1996;5644-5645 (b) Stork G., Brizzolara A., Landesman H., Szmuszkovitz J., Terrell R. J. Am. Chem. Soc. 85:1963;207-222 (c) Tokumitsu T., Hayashi T. J. Org. Chem. 50:1985;1547-1550.
    • (1963) J. Am. Chem. Soc. , vol.85 , pp. 207-222
    • Stork, G.1    Brizzolara, A.2    Landesman, H.3    Szmuszkovitz, J.4    Terrell, R.5
  • 27
    • 0001128162 scopus 로고
    • Regioselective α-bromination of (Z)-5-substituted-2-alkylidene-4-oxothiazolidine derivatives
    • Regioselective α-bromination of (Z)-5-substituted-2-alkylidene-4-oxothiazolidine derivatives 3a-d, affording under mild experimental conditions vinyl bromides in good yields, reflects the enaminic susceptibility toward electrophiles, for additional examples see (a) Kordik C.P., Reitz A.B. J. Org. Chem. 61:1996;5644-5645 (b) Stork G., Brizzolara A., Landesman H., Szmuszkovitz J., Terrell R. J. Am. Chem. Soc. 85:1963;207-222 (c) Tokumitsu T., Hayashi T. J. Org. Chem. 50:1985;1547-1550.
    • (1985) J. Org. Chem. , vol.50 , pp. 1547-1550
    • Tokumitsu, T.1    Hayashi, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.