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Volumn 36, Issue 6, 2006, Pages 789-794

Efficient method for synthesis of the derivatives of 5-arylidene barbituric acid catalyzed by aminosulfonic acid with grinding

Author keywords

5 arylidene barbituric acid; Aminosulfonic acid; Aromatic aldehyde; Barbituric acid; Grinding method

Indexed keywords

ALDEHYDE; AMINOSULFONIC ACID; BARBITURIC ACID DERIVATIVE; SOLVENT; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 32644478411     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910500451324     Document Type: Article
Times cited : (45)

References (15)
  • 2
    • 0034933807 scopus 로고    scopus 로고
    • A simple method for Knoevenagel condensation of α,β-conjugated and aromatic aldehydes with barbituric acid
    • and reference therein
    • (b) Jursic, B. S. A simple method for Knoevenagel condensation of α,β-conjugated and aromatic aldehydes with barbituric acid. J. Heterocycl. Chem. 2001, 38, 655-657 and reference therein.
    • (2001) J. Heterocycl. Chem. , vol.38 , pp. 655-657
    • Jursic, B.S.1
  • 3
    • 0026517009 scopus 로고
    • Synthesis of oxadeazaflavines from barbituric acid and aromatic aldehydes
    • (a) Figueroa-Villar, J. D.; Rangel, C. E.; Dos Santos, L. N. Synthesis of oxadeazaflavines from barbituric acid and aromatic aldehydes. Synth. Commun. 1992, 22 (8), 1159-1164;
    • (1992) Synth. Commun. , vol.22 , Issue.8 , pp. 1159-1164
    • Figueroa-Villar, J.D.1    Rangel, C.E.2    Dos Santos, L.N.3
  • 4
    • 0001017036 scopus 로고
    • Oxidation of thiol with 5-arylidene-1,3-dimethylbarbituric acids: Application to synthesis of unsymmetrical disulfide
    • (b) Tanka, K.; Cheng, X.; Yoneda, F. Oxidation of thiol with 5-arylidene-1,3-dimethylbarbituric acids: Application to synthesis of unsymmetrical disulfide. Tetrahedron 1988, 44 (11), 3241.
    • (1988) Tetrahedron , vol.44 , Issue.11 , pp. 3241
    • Tanka, K.1    Cheng, X.2    Yoneda, F.3
  • 5
    • 0034077326 scopus 로고    scopus 로고
    • Preparation of benzylidene barbituric acids promoted by infrared irradiation in absence of solvent
    • and reference therein
    • Alcerreca, G.; Sanabria, R.; Miranda, R.; Arroyo, G.; Tamariz, J.; Delgado, F. Preparation of benzylidene barbituric acids promoted by infrared irradiation in absence of solvent. Synth. Commun. 2000, 30, 1295-1301 and reference therein.
    • (2000) Synth. Commun. , vol.30 , pp. 1295-1301
    • Alcerreca, G.1    Sanabria, R.2    Miranda, R.3    Arroyo, G.4    Tamariz, J.5    Delgado, F.6
  • 6
    • 0041929633 scopus 로고    scopus 로고
    • One-pot synthesis of barbiturates on reaction of barbituric acid with aldehydes under microwave irradiation using a variety of catalysts
    • Dewan, S. K.; Singh, R. One-pot synthesis of barbiturates on reaction of barbituric acid with aldehydes under microwave irradiation using a variety of catalysts. Synth. Commun. 2003, 33, 3081-3084.
    • (2003) Synth. Commun. , vol.33 , pp. 3081-3084
    • Dewan, S.K.1    Singh, R.2
  • 7
    • 32644463865 scopus 로고    scopus 로고
    • The condensation of aromatic aldehyde with barbituric acid, 2-thiobarbituric acid in water
    • Wan, Y.; Chen, J.; Zhuang, Q. Y.; Shi, D. Q. The condensation of aromatic aldehyde with barbituric acid, 2-thiobarbituric acid in water. J. Xuzhou Normal Univ. 2004, 22, 47-50.
    • (2004) J. Xuzhou Normal Univ. , vol.22 , pp. 47-50
    • Wan, Y.1    Chen, J.2    Zhuang, Q.Y.3    Shi, D.Q.4
  • 8
    • 32644471138 scopus 로고    scopus 로고
    • Solid phase synthesis of 5-arylidene barbituric acid
    • Gao, Y.; Tu, S. J.; Zhou, J. F. Solid phase synthesis of 5-arylidene barbituric acid. Chin. J. App. Chem. 2002, 19, 499-500.
    • (2002) Chin. J. App. Chem. , vol.19 , pp. 499-500
    • Gao, Y.1    Tu, S.J.2    Zhou, J.F.3
  • 9
    • 0347035385 scopus 로고    scopus 로고
    • Study of the solid state reactions of barbituric acid and aromatic aldehyde
    • Li, G. S.; Li, J. C.; Wang, C.; Feng, S.; Li, X. L. Study of the solid state reactions of barbituric acid and aromatic aldehyde. Chem. J. Chin. Univ. 2001, 22, 2042-2044.
    • (2001) Chem. J. Chin. Univ. , vol.22 , pp. 2042-2044
    • Li, G.S.1    Li, J.C.2    Wang, C.3    Feng, S.4    Li, X.L.5
  • 10
    • 19944374090 scopus 로고    scopus 로고
    • Sulfamic acid: A very useful catalyst
    • Wang, B. Sulfamic acid: a very useful catalyst. Synlett 2005, 1342-1343.
    • (2005) Synlett , pp. 1342-1343
    • Wang, B.1
  • 12
    • 26444589070 scopus 로고    scopus 로고
    • An efficient and practical synthesis of bis(indolyl)methanes catalyzed by aminosulfonic acid under ultrasound
    • Li, J. T.; Dai, H. G.; Xu, W. Z.; Li, T. S. An efficient and practical synthesis of bis(indolyl)methanes catalyzed by aminosulfonic acid under ultrasound. Ultrason. Sonochem. 2005, 13, 24-27.
    • (2005) Ultrason. Sonochem. , vol.13 , pp. 24-27
    • Li, J.T.1    Dai, H.G.2    Xu, W.Z.3    Li, T.S.4
  • 13
    • 0141567802 scopus 로고    scopus 로고
    • Synthesis of α,α′-bis(substitutedbenzylidene)- cycloalkanones by a grinding method
    • Wang, S. X.; Li, J. T.; Geng, L. J. Synthesis of α,α′- bis(substitutedbenzylidene)-cycloalkanones by a grinding method. J. Chem. Res. 2003, 370-371.
    • (2003) J. Chem. Res. , pp. 370-371
    • Wang, S.X.1    Li, J.T.2    Geng, L.J.3
  • 14
    • 0036925885 scopus 로고    scopus 로고
    • Preparation of the derivatives of 5-arylidene barbituric acid by grinding method
    • Geng, L. J.; Wang, S. X.; Li, J. T.; Liu, C. H. Preparation of the derivatives of 5-arylidene barbituric acid by grinding method. Chin. J. Org. Chem. 2002, 22, 1047-1049.
    • (2002) Chin. J. Org. Chem. , vol.22 , pp. 1047-1049
    • Geng, L.J.1    Wang, S.X.2    Li, J.T.3    Liu, C.H.4
  • 15
    • 0038737165 scopus 로고    scopus 로고
    • Solvent-free Knoevenagel condensations and Michael additions in the solid state and in the melt with quantitative yield
    • Kanpp, G.; Naimi-Jamal, M. R.; Schmeyers, J. Solvent-free Knoevenagel condensations and Michael additions in the solid state and in the melt with quantitative yield. Tetrahedron 2003, 59, 3753-3760.
    • (2003) Tetrahedron , vol.59 , pp. 3753-3760
    • Kanpp, G.1    Naimi-Jamal, M.R.2    Schmeyers, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.