메뉴 건너뛰기




Volumn 40, Issue 4, 2010, Pages 615-623

Green, microwave-assisted approach to the synthesis of arylidene- substituted spiro[4,5]decan-8-one derivatives in water

Author keywords

Green synthesis; Microwave irradiation; Water

Indexed keywords

7,9 BIS (1 4 TOLYLMETHYLIDENE) 1,4 DIOXASPIRO[4,5]DECAN 8 ONE; 7,9 BIS (1 BENZO[1,3]DIOXOL 5 YLMETHYLIDENE) 1,4 DIOXASPIRO[4,5] DECAN 8 ONE; 7,9 BIS (1 THIOPHEN 2 YLMETHYLIDENE) 1,4 DIOXASPIRO[4,5]DECAN 8 ONE; 7,9 BIS [1 (2,4 DICHLOROPHENYL) METHYLIDENE] 1,4 DIOXASPIRO[4,5] DECAN 8 ONE; 7,9 BIS [1 (3 NITROPHENYL) METHYLIDENE] 1,4 DIOXASPIRO[4,5]DECAN 8 ONE; 7,9 BIS [1 (3,4,5 METHOXYPHENYL) METHYLIDENE] 1,4 DIOXASPIRO[4,5]DECAN 8 ONE; 7,9 BIS [1 (4 BROMOPHENYL) METHYLIDINE] 1,4 DIOXASPIRO[4,5]DECAN 8 ONE; 7,9 BIS [1 (4 CHLOROPHENYL) METHYLIDENE] 1,4 DIOXASPIRO[4,5]DECAN 8 ONE; 7,9 BIS [1 (4 DIMETHYLAMINOPHENYL) METHYLIDENE] 1,4 DIOXASPIRO[4,5] DECAN 8 ONE; 7,9 BIS [1 (4 FLUOROPHENYL) METHYLIDENE] 1,4 DIOXASPIRO[4,5]DECAN 8 ONE; 7,9 BIS [1 (4 METHOXYPHENYL) METHYLIDENE] 1,4 DIOXASPIRO[P4,5]DECAN 8 ONE; 7,9 BIS [1 (CHLOROPHENYL) METHYLIDENE] 1,4 DIOXASPIRO[4.5]DECAN 8 ONE; ALDEHYDE; DECANE; SPIRO COMPOUND; UNCLASSIFIED DRUG;

EID: 76149089208     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910903009471     Document Type: Article
Times cited : (1)

References (46)
  • 1
    • 76149106922 scopus 로고
    • Reactions of mono-and diarylidenecycloalkanones with thiourea and ammonium thiocyanate
    • Tamas, L.; Dezso, S.; Andras, N. Reactions of mono-and diarylidenecycloalkanones with thiourea and ammonium thiocyanate. Acta Chim. Acad. Sci. Hung. 1977, 93, 51.
    • (1977) Acta Chim. Acad. Sci. Hung , vol.93 , pp. 51
    • Tamas, L.1    Dezso, S.2    Andras, N.3
  • 2
    • 76149084265 scopus 로고
    • Reactions of mono-and diarylidenecycloalkanones with thiourea and ammonium thiocyanate III: Acylation and alkylation of 3, 4, 5,6,7,8-hexahydro- 2(1H)-quinazolinethiones
    • Tamas, L.; Dezso, S.; Andras, F. Reactions of mono-and diarylidenecycloalkanones with thiourea and ammonium thiocyanate, III: Acylation and alkylation of 3,4,5,6,7,8-hexahydro-2(1H)-quinazolinethiones. Acta Chim. Acad. Sci. Hung. 1980, 104, 147.
    • (1980) Acta Chim. Acad. Sci. Hung , vol.104 , pp. 147
    • Tamas, L.1    Dezso, S.2    Andras, F.3
  • 3
    • 0034721143 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of certain a,b-unsaturated ketones and their corresponding fused pyridines as antiviral and cytotoxic agents
    • El-Subbagh, H. I.; Abu-Zaid, S. M.; Mahran, M. A.; Badria, F. A.; Al-ObaidSubbagh, A. M. Synthesis and biological evaluation of certain a,b-unsaturated ketones and their corresponding fused pyridines as antiviral and cytotoxic agents. J. Med. Chem. 2000, 43, 2915.
    • (2000) J. Med. Chem , vol.43 , pp. 2915
    • El-Subbagh, H.I.1    Abu-Zaid, S.M.2    Mahran, M.A.3    Badria, F.A.4    Al-Obaidsubbagh, A.M.5
  • 4
    • 2542609347 scopus 로고    scopus 로고
    • Synthesis of novel spiro and fused cyclopenta[c]-pyrazole and-pyrimidine derivatives
    • Albar, H. A.; Makki, M. S. I.; Faidallah Albar, H. M. Synthesis of novel spiro and fused cyclopenta[c]-pyrazole and-pyrimidine derivatives. J. Chem. Res., Synop. 1997, 40.
    • (1997) J. Chem. Res. Synop , vol.40
    • Albar, H.A.1    Makki, M.S.I.2    Faidallah Albar, H.M.3
  • 5
    • 76149102674 scopus 로고
    • Reactions of mono-and diarylidenecy-cloalkanones with thiourea and ammonium thiocyanate VI: (Z)-(E)-isomerization of 2-alkylmercapto-4-phenyl-8- benzylidene-5, 6, 7,8-tetrahydroquinazolines
    • Tamas, L.; Dezso, S.; Andras, F.; Andras, N. Reactions of mono-and diarylidenecy-cloalkanones with thiourea and ammonium thiocyanate, VI: (Z)-(E)-isomerization of 2-alkylmercapto-4-phenyl-8-benzylidene-5,6,7,8- tetrahydroquinazolines. Acta Chim. Acad. Sci. Hung. 1982, 110, 31.
    • (1982) Acta Chim. Acad. Sci. Hung , vol.110 , pp. 31
    • Tamas, L.1    Dezso, S.2    Andras, F.3    Andras, N.4
  • 6
    • 0141777817 scopus 로고
    • Reactions with (arylmethylene)cycloalkanones 1: 2,6-Bis(arylmethylene) cyclohexanones
    • Ali, M. I.; Hammam, A. E. G. Reactions with (arylmethylene) cycloalkanones, 1: 2,6-Bis(arylmethylene)cyclohexanones. J. Chem. Eng. Data 1978, 23, 351.
    • (1978) J. Chem. Eng. Data , vol.23 , pp. 351
    • Ali, M.I.1    Hammam, A.E.G.2
  • 7
    • 0018347723 scopus 로고
    • Bicyclic pyrazolines, potential central nervous system depressants, and antiinflammatory agents
    • Krapcho, J. K.; Turk, C. F. Bicyclic pyrazolines, potential central nervous system depressants, and antiinflammatory agents. J. Med. Chem. 1979, 22, 207.
    • (1979) J. Med. Chem , vol.22 , pp. 207
    • Krapcho, J.K.1    Turk, C.F.2
  • 8
    • 0020279438 scopus 로고
    • Reactions of mono-and diarylidenecycloalkanones with thiourea and ammonium rhodanide VII: Synthesis of 2-alkylmercapto-4-phenylbenzo[h]- quinazolines
    • Tamas, L.; Dezso, S.; Andras, F. Reactions of mono-and diarylidenecycloalkanones with thiourea and ammonium rhodanide, VII: Synthesis of 2-alkylmercapto-4-phenylbenzo[h]-quinazolines. Acta Chim. Acad. Sci. Hung. 1982, 111, 305.
    • (1982) Acta Chim. Acad. Sci. Hung , vol.111 , pp. 305
    • Tamas, L.1    Dezso, S.2    Andras, F.3
  • 9
    • 0017571051 scopus 로고
    • Reactions of mono-and diarylidenecycloalkanones with thiourea and ammonium thiocyanate II: Synthesis of 4-aryl-2-imino-1, 2, 5,6,7,8-hexahydro-4H- 3,1-benzothiazine salts and 4-aryl-2-imino-1,2,4,5,6,7-hexahydrocyclopenta[d][1, 3]thiazine salts
    • Lorand, T.; Szabo, D. Reactions of mono-and diarylidenecycloalkanones with thiourea and ammonium thiocyanate, II: Synthesis of 4-aryl-2-imino-1,2,5,6, 7,8-hexahydro-4H-3,1-benzothiazine salts and 4-aryl-2-imino-1,2,4,5,6,7- hexahydrocyclopenta[d][1,3]thiazine salts. Acta Chim. Acad. Sci. Hung. 1977, 94, 363.
    • (1977) Acta Chim. Acad. Sci. Hung , vol.94 , pp. 363
    • Lorand, T.1    Szabo, D.2
  • 10
    • 2542511764 scopus 로고    scopus 로고
    • Novel synthesis of a new class of strongly fluorescent phenanthridine analogues
    • Elgemeie, G. H.; Attia, A. M. E.; Fathy, N. M. Novel synthesis of a new class of strongly fluorescent phenanthridine analogues. J. Chem. Res., Synop. 1997, 112.
    • (1997) J. Chem. Res. Synop , vol.112
    • Elgemeie, G.H.1    Attia, A.M.E.2    Fathy, N.M.3
  • 11
    • 76149098285 scopus 로고
    • A,b-Unsaturated nitriles in hetero-cyclic synthesis: A new synthetic route to condensed 2-alkoxy-4-aryl-3-cyanopyridines
    • Hamza, E. G.; Abdelmaksoud, A. F.; Khaled, A. H. a,b-Unsaturated nitriles in hetero-cyclic synthesis: A new synthetic route to condensed 2-alkoxy-4-aryl-3-cyanopyridines. J. Chem. Res., Synop. 1991, 128.
    • (1991) J. Chem. Res. Synop , vol.128
    • Hamza, E.G.1    Abdelmaksoud, A.F.2    Khaled, A.H.3
  • 13
    • 76149140173 scopus 로고
    • Synthesis of 2-amino-8-benzyli-dene-4-phenyl-3, 4, 5,6,7,8-hexahydro-and- 5,6,7,8-tetrahydroquinazoline derivatives
    • Jozsef, D.; Tamas, L.; Dezso, S.; Andras, F.; Adolf, Z. Synthesis of 2-amino-8-benzyli-dene-4-phenyl-3,4,5,6,7,8-hexahydro-and-5,6,7, 8-tetrahydroquinazoline derivatives. Collect. Czech. Chem. Commun. 1985, 50, 1603.
    • (1985) Collect. Czech. Chem. Commun , vol.50 , pp. 1603
    • Jozsef, D.1    Tamas, L.2    Dezso, S.3    Andras, F.4    Adolf, Z.5
  • 14
    • 84986506360 scopus 로고
    • Heterocycles part XII: Synthesis of new benzo[6, 7]-cyclohepta[1,2-d] pyrimidine
    • El-Rayyes, N. R.; Ramadan, H. M. Heterocycles, part XII: Synthesis of new benzo[6,7]-cyclohepta[1,2-d]pyrimidine. J. Heterocycl. Chem. 1987, 24, 1141.
    • (1987) J. Heterocycl. Chem , vol.24 , pp. 1141
    • El-Rayyes, N.R.1    Ramadan, H.M.2
  • 16
    • 0018159019 scopus 로고
    • Synthesis and evaluation of 1-(hydroxyphenyl)-1-nonen-3-ones and related compounds for antineoplastic and antimicrobial activities
    • (a) Dimmock, J. R.; Nyathi, C. B.; Smith, P. J. Synthesis and evaluation of 1-(hydroxyphenyl)-1-nonen-3-ones and related compounds for antineoplastic and antimicrobial activities. J. Pharm. Sci. 1978, 67, 1543.
    • (1978) J. Pharm. Sci , vol.67 , pp. 1543
    • Dimmock, J.R.1    Nyathi, C.B.2    Smith, P.J.3
  • 17
    • 0017296451 scopus 로고
    • Pyrido[2,3-d]pyrimidines IV: Synthetic studies leading to various oxopyrido[2,3-d]pyrimidines
    • (a) Broom, A. D.; Shim, J. L.; Anderson, G. L. Pyrido[2,3-d]pyrimidines, IV: Synthetic studies leading to various oxopyrido[2,3-d]pyrimidines. J. Org. Chem. 1976, 41, 1095;
    • (1976) J. Org. Chem , vol.41 , pp. 1095
    • Broom, A.D.1    Shim, J.L.2    Anderson, G.L.3
  • 18
    • 0018874182 scopus 로고
    • Synthesis and anti-tumor activity of 2, 4-diamino-6-(2,5-dimethoxybenzyl) -5-methylpyrido[2,3-d]pyrimidine
    • (a) Grivsky, E. M.; Lee, S.; Sigel, C. W.; Duch, D. S.; Nichol, C. A. Synthesis and anti-tumor activity of 2,4-diamino-6-(2,5-dimethoxybenzyl)-5- methylpyrido[2,3-d]pyrimidine. J. Med. Chem. 1980, 23, 327. (b)
    • (1980) J. Med. Chem , vol.23 , pp. 327
    • Grivsky, E.M.1    Lee, S.2    Sigel, C.W.3    Duch, D.S.4    Nichol, C.A.5
  • 19
    • 0016423037 scopus 로고
    • Pyrido[2,3-d]pyrimidine antibacterial agents 3: 8-Alkyl-and 8-vinyl-5,8-dihydro-5-oxo-2-(1-piperazinyl)pyrido[2,3-d]pyrimidine-6-carboxylic acids and their derivatives
    • (a) Matsumoto, J.; Minami, S. Pyrido[2,3-d]pyrimidine antibacterial agents, 3: 8-Alkyl-and 8-vinyl-5,8-dihydro-5-oxo-2-(1-piperazinyl)pyrido[2,3-d] pyrimidine-6-carboxylic acids and their derivatives. J. Med. Chem. 1975, 18, 74;
    • (1975) J. Med. Chem , vol.18 , pp. 74
    • Matsumoto, J.1    Minami, S.2
  • 20
    • 0019206445 scopus 로고
    • Synthesis of antimicrobial agents V: Synthesis and antimicrobial activities of some heterocyclic condensed 1,8-naphthyridine derivatives
    • (b) Suzuki, N. Synthesis of antimicrobial agents, V: Synthesis and antimicrobial activities of some heterocyclic condensed 1,8-naphthyridine derivatives. Chem. Pharm. Bull. 1980, 28, 761;
    • (1980) Chem. Pharm. Bull , Issue.28 , pp. 761
    • Suzuki, N.1
  • 21
    • 0002435006 scopus 로고
    • Polyazanaphthalenes IV: Further derivatives of 1, 3,5-and 1,3,8-triazanaphthalene
    • (c) Oakes, V.; Rydon, H. N. Polyazanaphthalenes, IV: Further derivatives of 1,3,5-and 1,3,8-triazanaphthalene. J. Chem. Soc. 1956, 4433;
    • (1956) J. Chem. Soc , pp. 4433
    • Oakes, V.1    Rydon, H.N.2
  • 23
    • 0001870835 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of 1-aryl-2-vinyl-7-methyl-1, 4-dihydropyrido[2,3-d]pyrimidin-4-one derivatives
    • (e) Zakharov, A. V.; Gavrilov, M. Y.; Novoselova, G. N.; Vakhrin, M. I.; Konshin, M. E. Synthesis and antimicrobial activity of 1-aryl-2-vinyl-7-methyl- 1,4-dihydropyrido[2,3-d]pyrimidin-4-one derivatives. Khim. Farm. Zh. 1996, 30, 39.
    • (1996) Khim. Farm. Zh , Issue.30 , pp. 39
    • Zakharov, A.V.1    Gavrilov, M.Y.2    Novoselova, G.N.3    Vakhrin, M.I.4    Konshin, M.E.5
  • 24
    • 0002864486 scopus 로고
    • Nitriles of 2-arylamino-5-carboxy(carbethoxy)-6-methylnicotinic acids and 1-aryl-6-carbethoxy-7-methyl-4-oxy-1,4-dihydropyrido-[2,3-d]pyrimidines: Synthesis and biological activity
    • Deyanov, A. B.; Niyazov, R. K.; Nazmetdinov, F. Y.; Syropyatov, B. Y.; Kolla, V. E.; Konshin, M. E. Amides, nitriles of 2-arylamino-5- carboxy(carbethoxy)-6-methylnicotinic acids and 1-aryl-6-carbethoxy-7-methyl-4- oxy-1,4-dihydropyrido-[2,3-d]pyrimidines: Synthesis and biological activity. Khim. Farm. Zh. 1991, 25, 26.
    • (1991) Khim. Farm. Zh , Issue.25 , pp. 26
    • Deyanov, A.B.1    Niyazov, R.K.2    Nazmetdinov, F.Y.3    Syropyatov, B.Y.4    Kolla, V.E.5    Amides, E.K.M.6
  • 25
    • 27644452545 scopus 로고    scopus 로고
    • Dihydropyrido[2,3-d]pyrimidines as a new class of antileishmanial agents
    • Agarwal, A.; Ashutosh, R.; Goyal, N.; Chauhan, P. M. S.; Gupta, S. Dihydropyrido[2,3-d]pyrimidines as a new class of antileishmanial agents. Bioorg. Med. Chem. 2005, 13, 6678.
    • (2005) Bioorg. Med. Chem , Issue.13 , pp. 6678
    • Agarwal, A.1    Ashutosh, R.2    Goyal, N.3    Chauhan, P.M.S.4    Gupta, S.5
  • 28
    • 34447097175 scopus 로고    scopus 로고
    • Microwave-assisted synthesis in water as solvent
    • (b) Dallinger, D.; Kappe, C. O. Microwave-assisted synthesis in water as solvent. Chem. Rev. 2007, 107, 2563.
    • (2007) Chem. Rev , vol.107 , pp. 2563
    • Dallinger, D.1    Kappe, C.O.2
  • 29
    • 0036703508 scopus 로고    scopus 로고
    • Stereoselective organic reactions in water
    • (a) Lindstroem, U. M. Stereoselective organic reactions in water. Chem. Rev. 2002, 102, 2751;
    • (2002) Chem. Rev , vol.102 , pp. 2751
    • Lindstroem, U.M.1
  • 30
    • 24044470646 scopus 로고    scopus 로고
    • Organic reactions in aqueous media with a focus on carbon-carbon bond formations: A decade update
    • (b) Li, C. J. Organic reactions in aqueous media with a focus on carbon-carbon bond formations: A decade update. Chem. Rev. 2005, 105, 3095;
    • (2005) Chem. Rev , vol.105 , pp. 3095
    • Li, C.J.1
  • 31
    • 32044438203 scopus 로고    scopus 로고
    • Acceleration of organic reactions through aqueous solvent effects
    • (c) Pirrung, M. C. Acceleration of organic reactions through aqueous solvent effects. Chem. Eur. J. 2006, 12, 1312;
    • (2006) Chem. Eur. J , vol.12 , pp. 1312
    • Pirrung, M.C.1
  • 32
    • 0037020384 scopus 로고    scopus 로고
    • Microwave-assisted reactions in organic synthesis-Are there any non-thermal microwave effects?
    • (d) Strauss, C. R. Microwave-assisted reactions in organic synthesis-Are there any non-thermal microwave effects? Comments. Angew. Chem., Int. Ed. 2002, 41, 3589;
    • (2002) Comments. Angew. Chem. Int. Ed , vol.41 , pp. 3589
    • Strauss, C.R.1
  • 33
    • 11144325118 scopus 로고    scopus 로고
    • Synthetic methods: Controlled microwave heating in modern organic synthesis
    • (e) Kappe, C. O. Synthetic methods: Controlled microwave heating in modern organic synthesis. Angew. Chem., Int. Ed. 2004, 43, 6250.
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 6250
    • Kappe, C.O.1
  • 34
    • 84924213784 scopus 로고
    • Invited review: Developments in microwave-assisted organic chemistry
    • (a) Strauss, C. R.; Trainor, R. W. Invited review: Developments in microwave-assisted organic chemistry. Aust. J. Chem. 1995, 48, 1665.
    • (1995) Aust. J. Chem , vol.48 , pp. 1665
    • Strauss, C.R.1    Trainor, R.W.2
  • 35
    • 0001300546 scopus 로고
    • Selective Diels-Alder reactions in aqueous solutions and suspensions
    • (a) Breslow, R.; Maitra, U.; Rideout, D. Selective Diels-Alder reactions in aqueous solutions and suspensions. Tetrahedron Lett. 1983, 24, 1901;
    • (1983) Tetrahedron Lett , vol.24 , pp. 1901
    • Breslow, R.1    Maitra, U.2    Rideout, D.3
  • 37
    • 0001138032 scopus 로고
    • The conformational equilibrium of chorismate in solution: Implications for the mechanism of the non-enzymic and the enzyme-catalyzed rearrangement of chorismate to prephenate
    • (a) Copely, S. D.; Knowles, J. R. The conformational equilibrium of chorismate in solution: Implications for the mechanism of the non-enzymic and the enzyme-catalyzed rearrangement of chorismate to prephenate. J. Am. Chem. Soc. 1987, 109, 5008;
    • (1987) J. Am. Chem. Soc , vol.109 , pp. 5008
    • Copely, S.D.1    Knowles, J.R.2
  • 39
    • 4444354683 scopus 로고    scopus 로고
    • Green chemical synthesis of fluorinated 1, 3,5-triaryl-s-triazines in aqueous medium under microwaves as potential antifungal agents
    • Anshu, D.; Kapil, A.; Meha, S.; Pritima, S. Green chemical synthesis of fluorinated 1,3,5-triaryl-s-triazines in aqueous medium under microwaves as potential antifungal agents. J. Fluorine Chem. 2004, 125, 1273.
    • (2004) J. Fluorine Chem , Issue.125 , pp. 1273
    • Anshu, D.1    Kapil, A.2    Meha, S.3    Pritima, S.4
  • 40
    • 24944511568 scopus 로고    scopus 로고
    • A simple and clean procedure for the synthesis of polyhydroacridine and quinoline derivatives: Reaction of Schiff base with 1,3-dicarbonyl compounds in aqueous medium
    • Wang, X. S.; Zhang, M. M.; Zeng, Z. S.; Shi, D. Q.; Tu, S. J.; Wei, X. Y.; Zong, Z. M. A simple and clean procedure for the synthesis of polyhydroacridine and quinoline derivatives: Reaction of Schiff base with 1,3-dicarbonyl compounds in aqueous medium. Tetrahedron Lett. 2005, 46, 7169.
    • (2005) Tetrahedron Lett , vol.46 , pp. 7169
    • Wang, X.S.1    Zhang, M.M.2    Zeng, Z.S.3    Shi, D.Q.4    Tu, S.J.5    Wei, X.Y.6    Zong, Z.M.7
  • 41
    • 0034703278 scopus 로고    scopus 로고
    • Ruthenium-catalyzed synthesis of quinolines from anilines and allylammonium chlorides in an aqueous medium via amine exchange reaction
    • Cho, C. S.; Kim, J. S.; Oh, B. H.; Kim, T. J.; Shim, S. C.; Yoon, N. S. Ruthenium-catalyzed synthesis of quinolines from anilines and allylammonium chlorides in an aqueous medium via amine exchange reaction. Tetrahedron 2000, 56, 7747.
    • (2000) Tetrahedron , vol.56 , pp. 7747
    • Cho, C.S.1    Kim, J.S.2    Oh, B.H.3    Kim, T.J.4    Shim, S.C.5    Yoon, N.S.6
  • 42
    • 0028808827 scopus 로고
    • Aqueous hydrotrope solution as a safer medium for microwave-enhanced Hantzsch dihydropyridine ester synthesis
    • Bhushan, K. M.; Vilas, G. G.; Ashish, C. A. Aqueous hydrotrope solution as a safer medium for microwave-enhanced Hantzsch dihydropyridine ester synthesis. Tetrahedron Lett. 1995, 36, 8083.
    • (1995) Tetrahedron Lett , vol.36 , pp. 8083
    • Bhushan, K.M.1    Vilas, G.G.2    Ashish, C.A.3
  • 43
    • 0001540666 scopus 로고    scopus 로고
    • Ruthenium-catalyzed synthesis of indoles from anilines and trialkanolammonium chlorides in an aqueous medium
    • Sik, C. C.; Hwang, K. J.; Chul, S. S. Ruthenium-catalyzed synthesis of indoles from anilines and trialkanolammonium chlorides in an aqueous medium. Tetrahedron Lett. 2000, 41, 1811.
    • (2000) Tetrahedron Lett , vol.41 , pp. 1811
    • Sik, C.C.1    Hwang, K.J.2    Chul, S.S.3
  • 44
    • 20844446841 scopus 로고    scopus 로고
    • Reactivity of epicatechin in aqueous glycine and glucose Maillard reaction models: Quenching of C2, C3, and C4 sugar fragments
    • Vandana, T. M.; Devin, P. G. Reactivity of epicatechin in aqueous glycine and glucose Maillard reaction models: Quenching of C2, C3, and C4 sugar fragments. J. Agric. Food Chem. 2005, 53, 4130.
    • (2005) J. Agric. Food Chem , vol.53 , pp. 4130
    • Vandana, T.M.1    Devin, P.G.2
  • 45
    • 0033860125 scopus 로고    scopus 로고
    • Influence of pyrolytic and aqueous-phase reactions on the mechanism of formation of Maillard products
    • Andrzej, W.; Varoujan, Y. A. Influence of pyrolytic and aqueous-phase reactions on the mechanism of formation of Maillard products. J. Agric. Food Chem. 2000, 48, 3549.
    • (2000) J. Agric. Food Chem , vol.48 , pp. 3549
    • Andrzej, W.1    Varoujan, Y.A.2
  • 46
    • 0037462396 scopus 로고    scopus 로고
    • Green chemistry approaches to the synthesis of 5-alkoxycarbonyl-4-aryl-3, 4-dihydropyrimidin-2(1H)-ones by a three-component coupling of one-pot condensation reaction: Comparison of ethanol, water, and solvent-free conditions
    • Bose, D. S.; Fatima, L.; Mereyala, B. H. Green chemistry approaches to the synthesis of 5-alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones by a three-component coupling of one-pot condensation reaction: comparison of ethanol, water, and solvent-free conditions. J. Org. Chem. 2003, 68, 587.
    • (2003) J. Org. Chem , vol.68 , pp. 587
    • Bose, D.S.1    Fatima, L.2    Mereyala, B.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.