메뉴 건너뛰기




Volumn , Issue 7, 2009, Pages 1118-1122

Synthesis of selenium-substituted pyrroles and pyrazol-3-ones

Author keywords

1,2 diaza 1,3 butadienes; Michael additions; Pyrazoles; Pyrroles; Selenium

Indexed keywords

1 (PHENYLSELENO)KETONE DERIVATIVE; 1,2 DIAZA 1,3 BUTADIENE DERIVATIVE; 1,3 BUTADIENE DERIVATIVE; 2 MERCAPTOBENZOSELENAZOLE; 3 METHYL 5 OXO N PHENYL 4 (PHENYLSELENO) 2,5 DIHYDRO 1H PYRAZOLE 1 CARBOXAMIDE; 4 (1,3 BENZOSELENAZOL 2 YLTHIO))PYRAZOL 3 ONE DERIVATIVE; 4 (PHENYLSELENO)PYRAZOL 3 ONE DERIVATIVE; 4 (PHENYLSELENO)PYROLE DERIVATIVE; 5 ETHYL 4 (PHENYLSELENO) 1,2 DIHYDRO 3H PYRAZOL 3 ONE; ETHYL 1 [(AMINOCARBONYL)AMINO] 2,5 DIMETHYL 4 (PHENYLSELENO) 1H PYRROLE 3 CARBOXYLATE; HYDRAZONE DERIVATIVE; KETONE DERIVATIVE; PHENYLSELENOL; PYRAZOL 3 ONE DERIVATIVE; PYRAZOLE DERIVATIVE; PYRROLE DERIVATIVE; SELENIUM; UNCLASSIFIED DRUG;

EID: 67649532208     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0029-1216630     Document Type: Article
Times cited : (10)

References (43)
  • 1
    • 0001319053 scopus 로고
    • Katritzky, A. R.; Rees, C. W., Eds.; Pergamon Press: Oxford
    • (a) Sundberg, R. J. In Comprehensive Heterocyclic Chemistry, Vol.4; Katritzky, A. R.; Rees, C. W., Eds.; Pergamon Press: Oxford, 1984, 314.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.4 , pp. 314
    • Sundberg, R.J.1
  • 2
    • 0001275286 scopus 로고    scopus 로고
    • Katritzky, A. R.; Rees, C. W.; Scriven, E. F. V., Eds.; Pergamon-Elsevier Science: Amsterdam, Chap. 4
    • (b) Gribble, G. W. In Comprehensive Heterocyclic Chemistry II, Vol.2; Katritzky, A. R.; Rees, C. W.; Scriven, E. F. V., Eds.; Pergamon-Elsevier Science: Amsterdam, 1996, Chap. 4.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.2
    • Gribble, G.W.1
  • 4
    • 77956668922 scopus 로고    scopus 로고
    • Gribble, G. W.; Joule, J. A., Eds.; Elsevier: Oxford
    • Progress in Heterocyclic Chemistry, Vol.15-20; Gribble, G. W.; Joule, J. A., Eds.; Elsevier: Oxford, 2003-2008.
    • (2003) Progress in Heterocyclic Chemistry , vol.15-20
  • 14
    • 0001564719 scopus 로고    scopus 로고
    • Attanasi, O. A.; Spinelli, D., Eds.; Research Signpost: Trivandrum
    • (a) Attanasi, O. A.; Filippone, P. In Topics in Heterocyclic Systems, Vol.1; Attanasi, O. A.; Spinelli, D., Eds.; Research Signpost: Trivandrum, 1996, 157.
    • (1996) Topics in Heterocyclic Systems , vol.1 , pp. 157
    • Attanasi, O.A.1    Filippone, P.2
  • 25
    • 33749450027 scopus 로고    scopus 로고
    • Special issue
    • (i) Special issue: Curr. Org. Chem. 2006, 10, 1891.
    • (2006) Curr. Org. Chem. , vol.10 , pp. 1891
  • 35
    • 67649461701 scopus 로고    scopus 로고
    • note
    • 2 = 85:15) to yield 2b in 40% yield.
  • 36
    • 0031038902 scopus 로고    scopus 로고
    • Spectral data of 2a and 2b are identical to those already described in the literature
    • (b) Spectral data of 2a and 2b are identical to those already described in the literature: Houllemare, D.; Ponthieux, S.; Outurquin, F.; Paulmier, C. Synthesis 1997, 101.
    • (1997) Synthesis , pp. 101
    • Houllemare, D.1    Ponthieux, S.2    Outurquin, F.3    Paulmier, C.4
  • 37
    • 67649504007 scopus 로고    scopus 로고
    • note
    • 4Se: C, 48.25; H, 5.31; N, 10.55. Found: C, 48.19; H, 5.39; N, 10.63.
  • 38
    • 67649485428 scopus 로고    scopus 로고
    • note
    • 3Se: C, 50.53; H, 5.04; N, 11.05. Found: C, 50.48; H, 5.21; N, 10.96.
  • 40
    • 67649504006 scopus 로고    scopus 로고
    • note
    • 6): δ = 14.3 (q), 16.4 (q), 59.9 (t), 82.3 (s), 122.4 (d), 123.7 (d), 125.0 (d), 126.1 (d), 137.8 (s), 156.8 (s), 157.8 (s), 168.7 (s), 172.4 (s), 180.3 (s).
  • 41
    • 67649495470 scopus 로고    scopus 로고
    • note
    • 2SSe: C, 50.35; H, 3.29; N, 13.05. Found: C, 50.39; H, 3.31; N, 13.23.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.