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Volumn 40, Issue 7, 2010, Pages 1074-1081

Synthesis of tri-and disalicylaldehydes and their chiral schiff base compounds

Author keywords

5 Bromosalicylaldehyde; Disalicylaldehyde; Schiff base ligands; Trisalicylaldehyde

Indexed keywords

1,3,5 TRIS(4 HYDROXY 5 FORMYLPHENYL)BENZENE; 1,3,5 TRIS(4 METHOXY 5 FORMYLPHENYL)BENZENE; 4 BROMO 2 (DIETHOXYMETHYL) 1 METHOXYBENZENE; 4 METHOXY 3 FORMYLPHENYLBORONIC ACID; 4 METHOXY 4' HYDROXYL 3,3' DIFORMYL 1,1' DIPHENYL; 4,4' DIOL 3,3' DIFORMYL 1,1' DIPHENYL; 5 BROMO 2 METHOXYBENZALDEHYDE; DISALICYLALDEHYDE; SALICYLALDEHYDE; SCHIFF BASE; TRISALICYLALDEHYDE; UNCLASSIFIED DRUG;

EID: 77749280060     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910903040252     Document Type: Article
Times cited : (10)

References (21)
  • 1
    • 0141508049 scopus 로고    scopus 로고
    • Recent developments in the synthesis and utilization of chiral sulfoxides
    • Fernández, I; Khiar, N. Recent developments in the synthesis and utilization of chiral sulfoxides. Chem. Rev. 2003, 103(9), 3651-3670.
    • (2003) Chem. Rev , vol.103 , Issue.9 , pp. 3651-3670
    • Fernández, I.1    Khiar, N.2
  • 2
    • 0032568284 scopus 로고    scopus 로고
    • Schiff-base ligands carrying two elements of chirality: Matched-mismatched effects in the vanadium-catalyzed sulfoxidation of thioethers with hydrogen peroxide
    • (a) Vetter, A. H; Berkessel, A. Schiff-base ligands carrying two elements of chirality: Matched-mismatched effects in the vanadium-catalyzed sulfoxidation of thioethers with hydrogen peroxide. Tetrahedron Lett. 1998, 39, 1741-1744;.
    • (1998) Tetrahedron Lett , vol.39 , pp. 1741-1744
    • Vetter, A.H.1    Berkessel, A.2
  • 3
    • 9344221111 scopus 로고    scopus 로고
    • Efficient asymmetric oxidation of sulfides and kinetic resolution of sulfoxides catalyzed by a vanadium-salan system
    • (b) Sun, J; Zhu, C; Dai, Z; Yang, M; Pan, Y; Hu, H. Efficient asymmetric oxidation of sulfides and kinetic resolution of sulfoxides catalyzed by a vanadium-salan system. J. Org. Chem. 2004, 69, 8500-8503;.
    • (2004) J. Org. Chem , vol.69 , pp. 8500-8503
    • Sun, J.1    Zhu, C.2    Dai, Z.3    Yang, M.4    Pan, Y.5    Hu, H.6
  • 4
    • 29144501296 scopus 로고    scopus 로고
    • Vanadium-catalyzed enantioselective sulfoxidation and concomitant, highly efficient kinetic resolution provide high enantioselectivity and acceptable yields of sulfoxides
    • (c) Zeng, Q; Wang, H; Wang, T; Cai, Y; Weng, W; Zhao, Y. Vanadium-catalyzed enantioselective sulfoxidation and concomitant, highly efficient kinetic resolution provide high enantioselectivity and acceptable yields of sulfoxides. Adv. Synth. Catal. 2005, 347, 1933-1936.
    • (2005) Adv. Synth. Catal , vol.347 , pp. 1933-1936
    • Zeng, Q.1    Wang, H.2    Wang, T.3    Cai, Y.4    Weng, W.5    Zhao, Y.6
  • 5
    • 33846783022 scopus 로고    scopus 로고
    • Ring-expanding olefin metathesis: A route to highly active unsymmetrical macrocyclic oligomeric co-salen catalysts for the hydrolytic kinetic resolution of epoxides
    • (a) Zheng, X; Jones, C. W; Weck, M. Ring-expanding olefin metathesis: A route to highly active unsymmetrical macrocyclic oligomeric co-salen catalysts for the hydrolytic kinetic resolution of epoxides. J. Am. Chem. Soc. 2007, 129, 1105-1112;.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 1105-1112
    • Zheng, X.1    Jones, C.W.2    Weck, M.3
  • 6
    • 0036569687 scopus 로고    scopus 로고
    • Stereoselective recognition of an aziridine with a Co(III) complex: A potential transition-state analogue for catalytic epoxidation
    • (b) Bobb, R; Alhakimi, G; Studnicki, L; Chin, J. Stereoselective recognition of an aziridine with a Co(III) complex: A potential transition-state analogue for catalytic epoxidation. J. Am. Chem. Soc. 2002, 124, 4544-4545;.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 4544-4545
    • Bobb, R.1    Alhakimi, G.2    Studnicki, L.3    Chin, J.4
  • 7
    • 0032480681 scopus 로고    scopus 로고
    • Synthesis and characterization of a polymer-supported salen ligand for enantioselective epoxidation
    • (c) Angelino, M. D; Laibinis, P. E. Synthesis and characterization of a polymer-supported salen ligand for enantioselective epoxidation. Macromolecules 1998, 31, 7581-7587;.
    • (1998) Macromolecules , vol.31 , pp. 7581-7587
    • Angelino, M.D.1    Laibinis, P.E.2
  • 8
    • 2942642347 scopus 로고    scopus 로고
    • Catalytic asymmetric epoxidation of non-functionalised alkenes using polymeric Mn(III) salen as catalysts and NaOCl as oxidant
    • (d) Kureshy, R. I; Khan, N. H; Jasra, R. V. Catalytic asymmetric epoxidation of non-functionalised alkenes using polymeric Mn(III) salen as catalysts and NaOCl as oxidant. J. Mol. Catal. A: Chem. 2004, 218, 141-146.
    • (2004) J. Mol. Catal. A: Chem , vol.218 , pp. 141-146
    • Kureshy, R.I.1    Khan, N.H.2    Jasra, R.V.3
  • 9
    • 0034622902 scopus 로고    scopus 로고
    • Cyclopropanation of styrene catalyzed by Cu-(chiral Schiff-base) complexes
    • (a) Li, Z. N; Liu, G. S; Zheng, Z; Chen, H. L. Cyclopropanation of styrene catalyzed by Cu-(chiral Schiff-base) complexes. Tetrahedron: Asymmetry 2000, 56, 7187-7191;.
    • (2000) Tetrahedron: Asymmetry , vol.56 , pp. 7187-7191
    • Li, Z.N.1    Liu, G.S.2    Zheng, Z.3    Chen, H.L.4
  • 10
    • 0000904753 scopus 로고    scopus 로고
    • Chiral metallosalen complexes: Structures and catalyst tuning for asymmetric epoxidation and cyclopropanation
    • (b) Katsuki, T. Chiral metallosalen complexes: Structures and catalyst tuning for asymmetric epoxidation and cyclopropanation. Adv. Synth. Catal. 2002, 344, 131-147.
    • (2002) Adv. Synth. Catal , vol.344 , pp. 131-147
    • Katsuki, T.1
  • 11
    • 0000936493 scopus 로고    scopus 로고
    • Asymmetric hetero-Diels-Alder reactions catalyzed by chiral (salen) chromium(III) complexes
    • (a) Schaus, S. E; Branalt, J; Jacobsen, E. N. Asymmetric hetero-Diels-Alder reactions catalyzed by chiral (salen) chromium(III) complexes. J. Org. Chem. 1998, 63, 403-405;.
    • (1998) J. Org. Chem , vol.63 , pp. 403-405
    • Schaus, S.E.1    Branalt, J.2    Jacobsen, E.N.3
  • 12
    • 0035961115 scopus 로고    scopus 로고
    • Asymmetric hetero-Diels-Alder reaction using chiral cationic metallosalen complexes as catalysts
    • (b) Aikawa, K; Irie, R; Katsuki, T. Asymmetric hetero-Diels-Alder reaction using chiral cationic metallosalen complexes as catalysts. Tetrahedron 2001, 57, 845-851.
    • (2001) Tetrahedron , vol.57 , pp. 845-851
    • Aikawa, K.1    Irie, R.2    Katsuki, T.3
  • 13
    • 35348976022 scopus 로고    scopus 로고
    • Synthesis of 3-aryl-5-t-butyl-salicylaldehydes and their chiral Schiff base compounds
    • Liu, H; Wang, M; Wang, Y; Gu, Q; Sun, L. Synthesis of 3-aryl-5-t-butyl-salicylaldehydes and their chiral Schiff base compounds. Synth. Commun. 2007, 37, 3815-3.
    • (2007) Synth. Commun , vol.37 , pp. 3815-3826
    • Liu, H.1    Wang, M.2    Wang, Y.3    Gu, Q.4    Sun, L.5
  • 14
    • 51349108362 scopus 로고    scopus 로고
    • Influence of substituents in the salicylaldehyde-derived Schiff bases on vanadium-catalyzed asymmetric oxidation of sulfides
    • Liu, H; Wang, M; Wang, Y; Yin, R; Sun, L. Influence of substituents in the salicylaldehyde-derived Schiff bases on vanadium-catalyzed asymmetric oxidation of sulfides. Appl. Organometal. Chem. 2008, 22, 253-257.
    • (2008) Appl. Organometal. Chem , vol.22 , pp. 253-257
    • Liu, H.1    Wang, M.2    Wang, Y.3    Yin, R.4    Sun, L.5
  • 16
    • 22044448732 scopus 로고    scopus 로고
    • Homocoupling of aryl iodides and bromides using a palladium=indium bimetallic system
    • (a) Chang, Y. M; Lee, S. H; Cho, M. Y; Yoo, B. W; Rhee, H. J; Lee, S. H; Yoon, C. M. Homocoupling of aryl iodides and bromides using a palladium=indium bimetallic system. Synth. Commun. 2005, 35, 1851-1857;.
    • (2005) Synth. Commun , vol.35 , pp. 1851-1857
    • Chang, Y.M.1    Lee, S.H.2    Cho, M.Y.3    Yoo, B.W.4    Rhee, H.J.5    Lee, S.H.6    Yoon, C.M.7
  • 18
    • 37249071738 scopus 로고    scopus 로고
    • The double oxa-Michael-aldol condensation: Straightforward access to dimeric tetrahydroxanthenones
    • (c) Nising, C. F; Friedrich, A; Braese, S. The double oxa-Michael-aldol condensation: Straightforward access to dimeric tetrahydroxanthenones. Synlett 2007, 19, 2987-2990
    • (2007) Synlett , vol.19 , pp. 2987-2990
    • Nising, C.F.1    Friedrich, A.2    Braese, S.3
  • 19
    • 84928778249 scopus 로고
    • Tetrakis(triphenylphosphine)palladlum
    • Coulson, D. R. Tetrakis(triphenylphosphine)palladlum. Inorg. Synth. 1972, 13, 121-125.
    • (1972) Inorg. Synth , vol.13 , pp. 121-125
    • Coulson, D.R.1
  • 20
    • 0001391909 scopus 로고
    • Derivatives of phenylboric acid, their preparation and action upon bacteria II: Hydroxyphenylboric acids
    • Bean, F. R; Johnson, J. R. Derivatives of phenylboric acid, their preparation and action upon bacteria II: Hydroxyphenylboric acids. J. Am. Chem. Soc. 1932, 54, 4415-4425.
    • (1932) J. Am. Chem. Soc , vol.54 , pp. 4415-4425
    • Bean, F.R.1    Johnson, J.R.2
  • 21
    • 0001102595 scopus 로고
    • A Substituent control of intramolecular hydrogen bonding in formyl-protonated o-anisaldehydes: A stable ion and semiempirical MO investigation
    • Laali, K. K; Koser, J. G. F; Subramanyam, J. S; Forsyth, D. A. Substituent control of intramolecular hydrogen bonding in formyl-protonated o-anisaldehydes: A stable ion and semiempirical MO investigation. J. Org. Chem. 1993, 58, 1385-1392
    • (1993) J. Org. Chem , vol.58 , pp. 1385-1392
    • Laali, K.K.1    Koser, J.G.F.2    Subramanyam, J.S.3    Forsyth, D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.