-
2
-
-
52249086944
-
Bioactivity of Flavonoids on Insulin- Secreting Cells
-
P. Montserrat, A. Castell, I. Baiges, G. Montagut, L. Arola and A. Ardévol, Bioactivity of Flavonoids on Insulin- Secreting Cells. Compr. Rev. Food Sci. F., 2008, 7, 299.
-
(2008)
Compr. Rev. Food Sci. F.
, vol.7
, pp. 299
-
-
Montserrat, P.1
Castell, A.2
Baiges, I.3
Montagut, G.4
Arola, L.5
Ardévol, A.6
-
4
-
-
63049125250
-
The impact of flavonoids on memory: Physiological and molecular considerations
-
J.P.E. Spencer, The impact of flavonoids on memory: physiological and molecular considerations. Chem. Soc. Rev., 2009, 38, 1152.
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 1152
-
-
Spencer, J.P.E.1
-
5
-
-
10044246299
-
Review of the flavonoids quercetin, hesperetin, and naringenin. Dietary sources, bioactivities, bioavailability, and epidemiology Nutr
-
I. Erlund, Review of the flavonoids quercetin, hesperetin, and naringenin. Dietary sources, bioactivities, bioavailability, and epidemiology Nutr. Res., 2004, 24, 851.
-
(2004)
Res
, vol.24
, pp. 851
-
-
Erlund, I.1
-
6
-
-
0028798998
-
Anticancer and antioxidant activity of synthetic chalcones and related compounds
-
R.J. Anto, K. Sukumaran, G. Kuttan, M.N.A. Rao, V. Subbaraju and R. Kuttan, Anticancer and antioxidant activity of synthetic chalcones and related compounds. Cancer Lett. 1995, 97, 33.
-
(1995)
Cancer Lett
, vol.97
, pp. 33
-
-
Anto, R.J.1
Sukumaran, K.2
Kuttan, G.3
Rao, M.N.A.4
Subbaraju, V.5
Kuttan, R.6
-
7
-
-
17044456006
-
Analgesic and antiinflammatory effects of chalcones isolated from Myracrodruon urundeuva Allemão
-
C. Nakamura, N. Kawasako, H. Miyataka, E. Jayachandran, I. Kim, K. Kirk, T. Taguchi, H. Hori and T. Satoh, Analgesic and antiinflammatory effects of chalcones isolated from Myracrodruon urundeuva Allemão. Bioorg. Med. Chem. 2002, 10, 699.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 699
-
-
Nakamura, C.1
Kawasako, N.2
Miyataka, H.3
Jayachandran, E.4
Kim, I.5
Kirk, K.6
Taguchi, T.7
Hori, H.8
Satoh, T.9
-
8
-
-
0035077808
-
Synthetic and biological activity evaluation studies on novel 1, 3-diarylpropenones
-
S. Mukherjee, V. Kumar, A.K. Prasad, H.G. Raj, M.E. Bracke, C.E. Olsen, S.C. Jain and V.S. Parmar, Synthetic and biological activity evaluation studies on novel 1, 3-diarylpropenones. Bioorg. Med. Chem. 2001, 9, 337.
-
(2001)
Bioorg. Med. Chem.
, vol.9
, pp. 337
-
-
Mukherjee, S.1
Kumar, V.2
Prasad, A.K.3
Raj, H.G.4
Bracke, M.E.5
Olsen, C.E.6
Jain, S.C.7
Parmar, V.S.8
-
9
-
-
34047185373
-
Synthetic chalcones, flavanones, and flavones as antitumoral agents: Biological evaluation and structure-activity relationships
-
M. Cabrera, M. Simoens, G. Falchi, M.L. Lavaggi, O.E. Piro, E.E. Castellano, A. Vidal, A. Azqueta, A. Monge, A. López de Ceráin, G. Sagrera, G Seoane, H. Cerecetto and M. González, Synthetic chalcones, flavanones, and flavones as antitumoral agents: biological evaluation and structure-activity relationships. Bioorg. Med. Chem. 2007, 15, 3356.
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 3356
-
-
Cabrera, M.1
Simoens, M.2
Falchi, G.3
Lavaggi, M.L.4
Piro, O.E.5
Castellano, E.E.6
Vidal, A.7
Azqueta, A.8
Monge, A.9
de López, C.A.10
Sagrera, G.11
Seoane, G.12
Cerecetto, H.13
González, M.14
-
10
-
-
77955336343
-
Identification of chalcones as in vivo liver monofunctional phase II enzymes inducers
-
M. Cabrera, M.L. Lavaggi, L. Croce, L. Celano, L. Thomson, M. Fernández, C. Pintos, S. Raymondo, M. Bollati, A. Monge, A. López de Ceráin, O.E. Piro, H. Cerecetto, and M. González, Identification of chalcones as in vivo liver monofunctional phase II enzymes inducers. Bioorg. Med. Chem. 2010, 18, 5391.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 5391
-
-
Cabrera, M.1
Lavaggi, M.L.2
Croce, L.3
Celano, L.4
Thomson, L.5
Fernández, M.6
Pintos, C.7
Raymondo, S.8
Bollati, M.9
Monge, A.10
López de Ceráin, A.11
Piro, O.E.12
Cerecetto, H.13
González, M.14
-
11
-
-
0002898584
-
The antioxidants of higher plants
-
S.D. Dziedzic and B.J.F. Hudson, The antioxidants of higher plants. Food Chem., 1984, 14, 45.
-
(1984)
Food Chem
, vol.14
, pp. 45
-
-
Dziedzic, S.D.1
Hudson, B.J.F.2
-
12
-
-
0038623968
-
Dihydrochalcones: Evaluation as novel radical scavenging antioxidants
-
Y. Nakamura, S. Watanabe, N. Miyake, H. Kohno and T. Osawa, Dihydrochalcones: evaluation as novel radical scavenging antioxidants. J. Agric. Food Chem., 2003, 51, 3309.
-
(2003)
J. Agric. Food Chem.
, vol.51
, pp. 3309
-
-
Nakamura, Y.1
Watanabe, S.2
Miyake, N.3
Kohno, H.4
Osawa, T.5
-
13
-
-
0032542331
-
Chemoprotective properties of phenylpropenoids, bis(benzylidene)cycloalkanones, and related michael reaction acceptors: Correlation of potencies as phase 2 enzyme inducers and radical scavengers
-
A.T. Dinkova-Kostova, C. Abeygunawardana and P. Talalay, Chemoprotective properties of phenylpropenoids, bis(benzylidene)cycloalkanones, and related michael reaction acceptors: Correlation of potencies as phase 2 enzyme inducers and radical scavengers. J. Med. Chem., 1998, 41, 5296.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 5296
-
-
Dinkova-Kostova, A.T.1
Abeygunawardana, C.2
Talalay, P.3
-
14
-
-
76649126729
-
Screening of biological activities of a series of chalcone derivatives against human pathogenic microorganisms
-
Karaman, H. Gezegen, M.B. Gurdere, A. Dingil, and M. Ceylan, Screening of biological activities of a series of chalcone derivatives against human pathogenic microorganisms. Chem. Biodivers. 2010, 7, 400.
-
(2010)
Chem. Biodivers.
, vol.7
, pp. 400
-
-
Karaman1
Gezegen, H.2
Gurdere, M.B.3
Dingil, A.4
Ceylan, M.5
-
15
-
-
85200277245
-
Chalcones and flavonoids as anti-tuberculosis agents
-
Y.M. Lin, Y. Zhou, M.T. Flavin, L.M. Zhou, W. Nie, and F.C. Chen, Chalcones and flavonoids as anti-tuberculosis agents. Bioorg. Med. Chem. 2002, 10, 2802
-
Bioorg. Med. Chem.
, vol.2002
, pp. 10
-
-
Lin, Y.M.1
Zhou, Y.2
Flavin, M.T.3
Zhou, L.M.4
Nie, W.5
Chen, F.C.6
-
16
-
-
0033026925
-
The antileishmanial activity of novel oxygenated chalcones and their mechanism of action
-
L. Zhai, M. Chen, J. Blom, T.G. Theander, S.B. Christensen and A. Kharazmi, The antileishmanial activity of novel oxygenated chalcones and their mechanism of action. J. Antimicrob. Chemother., 1999, 43, 803
-
(1999)
J. Antimicrob. Chemother.
, vol.43
, pp. 803
-
-
Zhai, L.1
Chen, M.2
Blom, J.3
Theander, T.G.4
Christensen, S.B.5
Kharazmi, A.6
-
17
-
-
67650759608
-
Potent antimalarial activity of newly synthesized substituted chalcone analogs in vitro
-
S.K. Awasthi, N. Mishra, B. Kumar, M. Sharma, A. Bhattacharya, L.C. Mishra and V.K. Bhasin, Potent antimalarial activity of newly synthesized substituted chalcone analogs in vitro. Med. Chem. Res., 2009, 18, 407
-
(2009)
Med. Chem. Res.
, vol.18
, pp. 407
-
-
Awasthi, S.K.1
Mishra, N.2
Kumar, B.3
Sharma, M.4
Bhattacharya, A.5
Mishra, L.C.6
Bhasin, V.K.7
-
18
-
-
21044454550
-
Structural insight into the inhibition of acetylcholinesterase by 2, 3, 4, 5-tetrahydro-1, 5-benzothiazepines
-
F.L. Ansari, S. Umbreen, L. Hussain, T. Makhmoor, T.S.A. Nawaz, M.A. Lodhi, S.N. Khan, F. Shaheen, M.I. Choudhary and Atta-ur-Rahman, Structural insight into the inhibition of acetylcholinesterase by 2, 3, 4, 5-tetrahydro-1, 5-benzothiazepines. Chem. Biodivers., 2005, 2, 487.
-
(2005)
Chem. Biodivers.
, vol.2
, pp. 487
-
-
Ansari, F.L.1
Umbreen, S.2
Hussain, L.3
Makhmoor, T.4
Nawaz, T.S.A.5
Lodhi, M.A.6
Khan, S.N.7
Shaheen, F.8
Choudhary, M.I.9
Rahman, A.-U.10
-
19
-
-
79551669602
-
Liquiritigenin induces mitochondria-mediated apoptosis via cytochrome c release and caspases activation in HeLa Cells Phytother
-
C. Liu, Y. Wang, S. Xie, Y. Zhou, X. Ren, X. Li and Y. Cai, Liquiritigenin induces mitochondria-mediated apoptosis via cytochrome c release and caspases activation in HeLa Cells Phytother. Res., 2011, 25, 277
-
(2011)
Res
, vol.25
, pp. 277
-
-
Liu, C.1
Wang, Y.2
Xie, S.3
Zhou, Y.4
Ren, X.5
Li, X.6
Cai, Y.7
-
20
-
-
75149195318
-
A new series of flavones, thioflavones, and flavanones as selective monoamine oxidase- B inhibitors
-
F. Chimenti, R. Fioravanti, A. Bolasco, P. Chimenti, D. Secci, F. Rossi, M. Yáñez, F. Orallo, F. Ortuso, S. Alcaro, R. Cirilli, R. Ferretti and M.L. Sanna, A new series of flavones, thioflavones, and flavanones as selective monoamine oxidase- B inhibitors. Bioorg. Med. Chem., 2010, 18, 1273
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 1273
-
-
Chimenti, F.1
Fioravanti, R.2
Bolasco, A.3
Chimenti, P.4
Secci, D.5
Rossi, F.6
Yáñez, M.7
Orallo, F.8
Ortuso, F.9
Alcaro, S.10
Cirilli, R.11
Ferretti, R.12
Sanna, M.L.13
-
21
-
-
77956171708
-
Synthesis and biological activity of flavanone derivatives Bioorg
-
L. Shi, X.E. Feng, J.R. Cui, L.H. Fang, G.H. Du and Q.S. Li, Synthesis and biological activity of flavanone derivatives Bioorg. Med. Chem. Lett., 2010, 20, 5466
-
(2010)
Med. Chem. Lett.
, vol.20
, pp. 5466
-
-
Shi, L.1
Feng, X.E.2
Cui, J.R.3
Fang, L.H.4
Du, G.H.5
Li, Q.S.6
-
22
-
-
77957020511
-
Antifungal activity of natural and enzymatically-modified flavonoids isolated from citrus species
-
M.P. Sala, G. Céliz, H. Geronazzo, M. Daz and S.L. Resnik, Antifungal activity of natural and enzymatically-modified flavonoids isolated from citrus species. Food Chem., 2011, 124, 1411
-
(2011)
Food Chem
, vol.124
, pp. 1411
-
-
Sala, M.P.1
Céliz, G.2
Geronazzo, H.3
Daz, M.4
Resnik, S.L.5
-
23
-
-
77953906356
-
Identification of bioactive compounds from flowers of black elder (Sambucus nigra L.) that activate the human peroxisome proliferator-activated receptor (PPAR)γ
-
K.B. Christensen, R.K. Petersen, K. Kristiansen and L.P. Christensen, Identification of bioactive compounds from flowers of black elder (Sambucus nigra L.) that activate the human peroxisome proliferator-activated receptor (PPAR)γ. Phytother. Res., 2010, 24, S129.
-
(2010)
Phytother. Res.
, vol.24
-
-
Christensen, K.B.1
Petersen, R.K.2
Kristiansen, K.3
Christensen, L.P.4
-
24
-
-
71049127438
-
Hanrahan, 7-Hydroxy-benzopyran-4-one derivatives: A novel pharmacophore of peroxisome proliferator-activated receptor α and-γ (PPARα and γ) dual agonists
-
A. Matin, N. Gavande, M.S. Kim, N.X. Yang, N.K. Salam and J.R. Hanrahan, 7-Hydroxy-benzopyran-4-one derivatives: a novel pharmacophore of peroxisome proliferator-activated receptor α and-γ (PPARα and γ) dual agonists. J. Med. Chem., 2009, 52, 6835
-
(2009)
J. Med. Chem.
, vol.52
, pp. 6835
-
-
Matin, A.1
Gavande, N.2
Kim, M.S.3
Yang, N.X.4
Salam, N.K.5
-
25
-
-
77954212534
-
Synthesis of stilbene-fused 2'-hydroxychalcones and flavanones
-
I. Akçok and A. Çaǧir, Synthesis of stilbene-fused 2'-hydroxychalcones and flavanones. Bioorg. Chem., 2010, 38, 139.
-
(2010)
Bioorg. Chem.
, vol.38
, pp. 139
-
-
Akçok, I.1
Çaǧir, A.2
-
27
-
-
33645217958
-
Synthesis and PPAR-γ ligand-binding activity of the new series of 2'-hydroxychalcone and thiazolidinedione derivatives
-
S.H. Jung, S.Y. Park, Y. Kim- Pak, H.K. Lee, K.S. Park, K.H. Shin, K. Ohuchi, H.K. Shin, S.R. Keum and S.S. Lim, Synthesis and PPAR-γ ligand-binding activity of the new series of 2'-hydroxychalcone and thiazolidinedione derivatives. Chem. Pharm. Bull., 2006, 54, 368.
-
(2006)
Chem. Pharm. Bull.
, vol.54
, pp. 368
-
-
Jung, S.H.1
Park, S.Y.2
Kim-Pak, Y.3
Lee, H.K.4
Park, K.S.5
Shin, K.H.6
Ohuchi, K.7
Shin, H.K.8
Keum, S.R.9
Lim, S.S.10
-
28
-
-
19644369596
-
Preparative monohydroxyflavanone syntheses and a protocol for gas chromatography-mass spectrometry analysis of monohydroxyflavanones
-
H. Kagawa, A. Shigematsu, S. Ohta and Y. Harigaya, Preparative monohydroxyflavanone syntheses and a protocol for gas chromatography-mass spectrometry analysis of monohydroxyflavanones. Chem. Pharm. Bull., 2005, 5, 547
-
(2005)
Chem. Pharm. Bull.
, vol.5
, pp. 547
-
-
Kagawa, H.1
Shigematsu, A.2
Ohta, S.3
Harigaya, Y.4
-
29
-
-
34247877466
-
Acid catalyzed stereoselective rearrangement and dimerization of flavenes: Synthesis of dependensin
-
M. Deodhar, D.C. Black and N. Kumar, Acid catalyzed stereoselective rearrangement and dimerization of flavenes: synthesis of dependensin. Tetrahedron, 2007, 63, 5227
-
(2007)
Tetrahedron
, vol.63
, pp. 5227
-
-
Deodhar, M.1
Black, D.C.2
Kumar, N.3
-
30
-
-
0004494208
-
Photo-oxidative cyclisation of 2'-hydroxychalcones leading to flavones induced by heterocycle View the MathML source-oxides: High efficiency of pybimido[54-g]pteridine n-source-oxide for the photochemical dehydrogenation
-
Y. Maki, K. Shimada, M. Sako and R. Hirota, Photo-oxidative cyclisation of 2'-hydroxychalcones leading to flavones induced by heterocycle View the MathML source-oxides: high efficiency of pybimido[54-g]pteridine n-source-oxide for the photochemical dehydrogenation. Tetrahedron, 1988, 44, 3187
-
(1988)
Tetrahedron
, vol.44
, pp. 3187
-
-
Maki, Y.1
Shimada, K.2
Sako, M.3
Hirota, R.4
-
31
-
-
85200275876
-
Silica gel supported TaBr5: New catalyst for the facile and rapid cyclization of 2'-aminochalcones to the corresponding 2-aryl-2,3-dihydroquinolin-4(1H)-ones under solvent-free conditions
-
N. Ahmed and J.E. van Lier, Silica gel supported TaBr5: new catalyst for the facile and rapid cyclization of 2'-aminochalcones to the corresponding 2-aryl-2,3-dihydroquinolin-4(1H)-ones under solvent-free conditions. Terahedron. Lett., 2006, 47, 2725
-
Terahedron. Lett.
, vol.2006
, pp. 47
-
-
Ahmed, N.1
van Lier, J.E.2
-
32
-
-
0346692934
-
-
K. Maruyama, K. Tamanaka, and A. Nishinaga, Terahedron Lett., 1989, 30, 4145
-
(1989)
Terahedron Lett
, vol.30
, pp. 4145
-
-
Maruyama, K.1
Tamanaka, K.2
Nishinaga, A.3
-
33
-
-
13244291574
-
Conversion of 2'-hydroxychalcones to flavanones catalyzed by cobalt Schiff base complex
-
B.M. Choudary, K.V.S. Ranganath, J. Yadav and M.L. Kantam, Conversion of 2'-hydroxychalcones to flavanones catalyzed by cobalt Schiff base complex. Terahedron Lett., 2005, 46, 1369.
-
(2005)
Terahedron Lett
, vol.46
, pp. 1369
-
-
Choudary, B.M.1
Ranganath, K.V.S.2
Yadav, J.3
Kantam, M.L.4
-
34
-
-
74049153430
-
Efficient synthesis of chalcone derivatives catalyzed by re-usable hydroxyapatite
-
H. Solhy, R. Tahir, S. Sebti, R. Skouta, M. Bousmina, M. Zahouily and M. Larzek, Efficient synthesis of chalcone derivatives catalyzed by re-usable hydroxyapatite. Appl. Catal., A., 2010, 374, 189
-
(2010)
Appl. Catal., A.
, vol.374
, pp. 189
-
-
Solhy, H.1
Tahir, R.2
Sebti, S.3
Skouta, R.4
Bousmina, M.5
Zahouily, M.6
Larzek, M.7
-
35
-
-
77953412328
-
3: A suitable heterogeneous catalyst for the synthesis of flavones under microwave irradiation
-
3: A suitable heterogeneous catalyst for the synthesis of flavones under microwave irradiation. Int. J. Chem. Tech. Res., 2009, 1, 539
-
(2009)
Int. J. Chem. Tech. Res.
, vol.1
, pp. 539
-
-
Sarda, S.R.1
Jadhav, W.N.2
Pawar, R.P.3
-
36
-
-
0030869652
-
Convenient synthesis of α,α1- bis(substituted furfurylidene)cycloalkanones and -chalcones under microwave irradiation
-
G. Babu and P.T. Perumal, Convenient synthesis of α,α1- bis(substituted furfurylidene)cycloalkanones and -chalcones under microwave irradiation. Synth. Comm., 1997, 27, 3677
-
(1997)
Synth Comm
, vol.27
, pp. 3677
-
-
Babu, G.1
Perumal, P.T.2
-
37
-
-
65249174118
-
Fast and robust route to hydroporphyrin-chalcones with extended red or near-infrared absorption
-
C. Ruzié, M. Krayer and J.S. Lindsey, Fast and robust route to hydroporphyrin-chalcones with extended red or near-infrared absorption. Org. Lett., 2009, 11, 1761
-
(2009)
Org. Lett.
, vol.11
, pp. 1761
-
-
Ruzié, C.1
Krayer, M.2
Lindsey, J.S.3
-
38
-
-
69749120083
-
Optimizations of reaction parameters of microwave enhanced synthesis of 4,4-Dihydroxychalcone
-
B. Sharma, Optimizations of reaction parameters of microwave enhanced synthesis of 4,4-Dihydroxychalcone. Asian J. Chem., 2009, 21, 4233
-
(2009)
Asian J. Chem.
, vol.21
, pp. 4233
-
-
Sharma, B.1
-
39
-
-
48249147819
-
Microwave studies on the synthesis of biologically active chalcone derivatives
-
S. Katade, U. Phalgune, S. Biswas, R. Wakharkar and N. Deshpande, Microwave studies on the synthesis of biologically active chalcone derivatives. Ind. J. Chem., 2008, 47B, 927
-
(2008)
Ind. J. Chem.
, vol.47 B
, pp. 927
-
-
Katade, S.1
Phalgune, U.2
Biswas, S.3
Wakharkar, R.4
Deshpande, N.5
-
40
-
-
34547860905
-
Solvent free microwave assisted synthesis of chalcones and their antifungal activities
-
R.K. Saini, N. Kumari, Y.C. Joshi, P. Joshi and S.S. Shekhawat, Solvent free microwave assisted synthesis of chalcones and their antifungal activities. Asian J. Chem., 2007, 19, 4483
-
(2007)
Asian J. Chem.
, vol.19
, pp. 4483
-
-
Saini, R.K.1
Kumari, N.2
Joshi, Y.C.3
Joshi, P.4
Shekhawat, S.S.5
-
41
-
-
38349050363
-
The synthesis, characterization and properties of coumarin-based chromophores containing a chalcone moiety
-
Y.F. Sun and Y.P. Cui, The synthesis, characterization and properties of coumarin-based chromophores containing a chalcone moiety. Dyes Pigments, 2008, 78, 65
-
(2008)
Dyes Pigments
, vol.78
, pp. 65
-
-
Sun, Y.F.1
Cui, Y.P.2
-
42
-
-
0032865475
-
Simple access to α, β unsaturated ketones by acid-catalyzed solvent-free reactions
-
E. Le Gall, F. Texier-Boullet and J. Hamelin, Simple access to α, β unsaturated ketones by acid-catalyzed solvent-free reactions. Synth. Comm., 1999, 29, 3651.
-
(1999)
Synth. Comm.
, vol.29
, pp. 3651
-
-
Le Gall, E.1
Texier-Boullet, F.2
Hamelin, J.3
-
43
-
-
85200278347
-
Efficient liquidphase synthesis of 2'-hydroxychalcones
-
E.V. Stoyanov, Y. Champavier, A. Simon and J.P. Basly, Efficient liquidphase synthesis of 2'-hydroxychalcones. Bioorg. Med. Chem. Lett., 2002, 12, 2685
-
Bioorg. Med. Chem. Lett.
, vol.2002
, pp. 12
-
-
Stoyanov, E.V.1
Champavier, Y.2
Simon, A.3
Basly, J.P.4
-
44
-
-
70350004821
-
A facile microwave assisted synthesis of flavones
-
M.J. Menezes, S. Manjrekar, V. Pai, R.E. Patre and S.G. Tilve, A facile microwave assisted synthesis of flavones. Indian J. Chem., Sect B, 2009, 48, 1311
-
(2009)
Indian J. Chem., Sect B.
, vol.48
, pp. 1311
-
-
Menezes, M.J.1
Manjrekar, S.2
Pai, V.3
Patre, R.E.4
Tilve, S.G.5
-
45
-
-
85200276406
-
Microwave- accelerated SPOT-synthesis on cellulose supports
-
M.D. Bowman, R.C. Jeske and H.E. Blackwell, Microwave- accelerated SPOT-synthesis on cellulose supports. Org. Lett., 2004, 6, 2019
-
Org. Lett.
, vol.2004
, pp. 6
-
-
Bowman, M.D.1
Jeske, R.C.2
Blackwell, H.E.3
-
46
-
-
33645959862
-
Efficient synthesis of small molecule macroarrays: Optimization of the macroarray synthesis platform and examination of microwave and conventional heating methods
-
M.D. Bowman, M.M. Jacobsen, B.G. Pujanauski and H.E. Blackwell, Efficient synthesis of small molecule macroarrays: optimization of the macroarray synthesis platform and examination of microwave and conventional heating methods. Tetrahedron, 2006, 62, 4715.
-
(2006)
Tetrahedron
, vol.62
, pp. 4715
-
-
Bowman, M.D.1
Jacobsen, M.M.2
Pujanauski, B.G.3
Blackwell, H.E.4
-
47
-
-
85200275169
-
K. 2,6,8-Trisubstituted 3- hydroxychromone derivatives as fluorophores for live-cell imaging
-
M. Fridén-Saxin, N. Pemberton, K. da Silva Andersson, C. Dyrager, A. Friberg, M. Grøtli and K. Luthman, K. 2,6,8-Trisubstituted 3- hydroxychromone derivatives as fluorophores for live-cell imaging. J. Org. Chem., 2009, 74, 2755.
-
J. Org. Chem.
, vol.2009
, pp. 74
-
-
Fridén-Saxin, M.1
Pemberton, N.2
da Silva Andersson, K.3
Dyrager, C.4
Friberg, A.5
Grøtli, M.6
Luthman, K.7
-
48
-
-
24044534767
-
Microwave accelerated solvent-free synthesis of flavanones
-
G.J. Sagrera and G.A. Seoane, Microwave accelerated solvent-free synthesis of flavanones. J. Braz. Chem. Soc., 2005, 16, 851
-
(2005)
J. Braz. Chem. Soc.
, vol.16
, pp. 851
-
-
Sagrera, G.J.1
Seoane, G.A.2
-
49
-
-
0035911022
-
Highly diastereoselective Michael reaction under solvent-free conditions using microwaves: Conjugate addition of flavanone to its chalcone precursor
-
T. Patonay, R.S. Varma, A. Vass, A. Lévai and J. Dudás, Highly diastereoselective Michael reaction under solvent-free conditions using microwaves: conjugate addition of flavanone to its chalcone precursor. Terahedron Lett., 2001, 42, 1403.
-
(2001)
Terahedron Lett
, vol.42
, pp. 1403
-
-
Patonay, T.1
Varma, R.S.2
Vass, A.3
Lévai, A.4
Dudás, J.5
-
50
-
-
79953819148
-
Rapid and efficient protic ionic liquidmediated pinacol rearrangements under microwave irradiation
-
L.C. Henderson and N. Byrne, Rapid and efficient protic ionic liquidmediated pinacol rearrangements under microwave irradiation. Green. Chem. 2011, 13, 813
-
(2011)
Green. Chem.
, vol.13
, pp. 813
-
-
Henderson, L.C.1
Byrne, N.2
-
51
-
-
77953315495
-
A facile, protic ionic liquid route to N-substituted 5-hydroxy-4-methyl-3-oxoisoindoline-1- carboxamides and N-substituted 3-oxoisoindoline-4-carboxylic acids
-
C.P. Gordon, N. Byrne and A. McCluskey, A facile, protic ionic liquid route to N-substituted 5-hydroxy-4-methyl-3-oxoisoindoline-1- carboxamides and N-substituted 3-oxoisoindoline-4-carboxylic acids. Green Chem., 2010, 12, 1000.
-
(2010)
Green Chem
, vol.12
, pp. 1000
-
-
Gordon, C.P.1
Byrne, N.2
McCluskey, A.3
-
52
-
-
0348110657
-
Ionic liquids by proton transfer: Vapor pressure, conductivity, and the relevance of ΔpK a from Aqueous Solutions
-
M. Yoshizawa, W. Xu and C.A. Angell, Ionic liquids by proton transfer: vapor pressure, conductivity, and the relevance of ΔpK a from Aqueous Solutions. J. Am. Chem. Soc., 2003, 125, 15411.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 15411
-
-
Yoshizawa, M.1
Xu, W.2
Angell, C.A.3
-
53
-
-
78649760794
-
4 in ionic liquid medium
-
A.R. Hajipour and F. Rafiee, Mild oxidative deprotection of aromatic hydrazones and semicarbazones with KMnO4 in ionic liquid medium. Org. Prep. Proced. Int., 2010, 42, 285
-
(2010)
Org. Prep. Proced. Int.
, vol.42
, pp. 285
-
-
Hajipour, A.R.1
Rafiee, F.2
-
54
-
-
77953682829
-
Protic ionic liquid [TMG][Ac] as an efficient, homogeneous and recyclable catalyst for Boc protection of amines
-
J. Akbari, A. Heydari, L. Ma'mani and H. Hassan, Protic ionic liquid [TMG][Ac] as an efficient, homogeneous and recyclable catalyst for Boc protection of amines. Comptes Rendus Chimie, 2010, 13, 544
-
(2010)
Comptes Rendus Chimie
, vol.13
, pp. 544
-
-
Akbari, J.1
Heydari, A.2
Ma'mani, L.3
Hassan, H.4
-
55
-
-
46949110592
-
The smallest amphiphiles: Nanostructure in protic room-temperature ionic liquids with short alkyl groups
-
R. Atkin and G. Warr, The smallest amphiphiles: nanostructure in protic room-temperature ionic liquids with short alkyl groups J. Phys. Chem. B., 2008, 112, 4164
-
(2008)
J. Phys. Chem. B.
, vol.112
, pp. 4164
-
-
Atkin, R.1
Warr, G.2
-
56
-
-
37349076236
-
Parallel developments in aprotic and protic ionic liquids: Physical chemistry and applications
-
C.A. Angell, N. Byrne and J.P. Belieres, Parallel developments in aprotic and protic ionic liquids: Physical chemistry and applications Acc. Chem. Res., 2007, 40, 1228
-
(2007)
Acc. Chem. Res.
, vol.40
, pp. 1228
-
-
Angell, C.A.1
Byrne, N.2
Belieres, J.P.3
-
57
-
-
34249741483
-
Protic ionic liquids: Preparation, characterization, and proton free energy level representation
-
J.P. Belieresand C.A. Angell, Protic ionic liquids: preparation, characterization, and proton free energy level representation. J. Phys. Chem. B., 2007, 111, 4926
-
(2007)
J. Phys. Chem. B.
, vol.111
, pp. 4926
-
-
Belieresand, J.P.1
Angell, C.A.2
-
58
-
-
85200275354
-
Protic ionic liquids: Solvents with tunable phase behavior and physicochemical properties
-
T.L. Greaves, A. Weerawardena, C. Fong, I. Krodkiewska and C.J. Drummond, Protic ionic liquids: solvents with tunable phase behavior and physicochemical properties. Chem. Commun., 2006, 110, 22479
-
Chem. Commun.
, vol.110
, Issue.2
, pp. 2006
-
-
Greaves, T.L.1
Weerawardena, A.2
Fong, C.3
Krodkiewska, I.4
Drummond, C.J.5
-
59
-
-
65249167660
-
Ultrastable superbase-derived protic ionic liquids
-
H. Luo, G.A. Baker, J.S. Lee, R. Pagni and S. Dai, Ultrastable superbase-derived protic ionic liquids. J. Phys. Chem. B., 2009, 113, 4181.
-
(2009)
J. Phys. Chem. B.
, vol.113
, pp. 4181
-
-
Luo, H.1
Baker, G.A.2
Lee, J.S.3
Pagni, R.4
Dai, S.5
-
60
-
-
37449026078
-
Asymmetric cyclization of 2'-hydroxychalcones to flavanones: Catalysis by chiral brønsted acids and bases
-
C. Dittmer, G. Raabe and L. Hintermann, Asymmetric cyclization of 2'-hydroxychalcones to flavanones: Catalysis by chiral brønsted acids and bases. Eur. J. Org. Chem., 2007, 5886
-
(2007)
Eur. J. Org. Chem.
, pp. 5886
-
-
Dittmer, C.1
Raabe, G.2
Hintermann, L.3
-
61
-
-
85200276779
-
Chemistry and biochemistry of plant substances. VII. Formation of hydroxychalcones and -flavanones
-
L. Reichel and W. Burkart, Chemistry and biochemistry of plant substances. VII. Formation of hydroxychalcones and -flavanones. Ber. Dtsch. Chem. Ges., 1941, 74, 1802.
-
(1941)
Ber. Dtsch. Chem. Ges.
, vol.74
, pp. 1802
-
-
Reichel, L.1
Burkart, W.2
-
62
-
-
34247167637
-
Catalytic enantioselective synthesis of flavanones and chromanones
-
M.M. Biddle, M. Lin and K.A. Scheidt, Catalytic enantioselective synthesis of flavanones and chromanones. J. Am. Chem. Soc., 2007, 129, 3830
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 3830
-
-
Biddle, M.M.1
Lin, M.2
Scheidt, K.A.3
-
63
-
-
55249112957
-
Asymmetric intramolecular oxa-michael addition of activated α,β-unsaturated ketones catalyzed by a chiral N,N'-dioxide nickel(II) complex: Highly enantioselective synthesis of flavanones
-
L. Wang, X. Liu, Z. Dong, X. Fu and X. Feng, Asymmetric intramolecular oxa-michael addition of activated α,β-unsaturated ketones catalyzed by a chiral N,N'-dioxide nickel(II) complex: Highly enantioselective synthesis of flavanones. Angew. Chem. Int. Ed., 2008, 47, 8670.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 8670
-
-
Wang, L.1
Liu, X.2
Dong, Z.3
Fu, X.4
Feng, X.5
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