-
1
-
-
84894639711
-
Green and sustainable manufacture of chemicals from biomass: State of the art
-
Sheldon, R. A. Green and sustainable manufacture of chemicals from biomass: State of the art Green Chem. 2014, 16, 950-963
-
(2014)
Green Chem.
, vol.16
, pp. 950-963
-
-
Sheldon, R.A.1
-
2
-
-
84874455368
-
Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
-
Alonso, D. M.; Wettstein, S. G.; Dumesic, J. A. Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass Green Chem. 2013, 15, 584-595
-
(2013)
Green Chem.
, vol.15
, pp. 584-595
-
-
Alonso, D.M.1
Wettstein, S.G.2
Dumesic, J.A.3
-
3
-
-
84887978889
-
Bio-based solvents: An emerging generation of fluids for the design of eco-efficient processes in catalysis and organic chemistry
-
Gu, Y.; Jerome, F. Bio-based solvents: An emerging generation of fluids for the design of eco-efficient processes in catalysis and organic chemistry Chem. Soc. Rev. 2013, 42, 9550-9570
-
(2013)
Chem. Soc. Rev.
, vol.42
, pp. 9550-9570
-
-
Gu, Y.1
Jerome, F.2
-
4
-
-
38849151682
-
γ-Valerolactone - A sustainable liquid for energy and carbon-based chemicals
-
Horváth, I. T.; Mehdi, H.; Fábos, V.; Boda, L.; Mika, L. T. γ-Valerolactone-A sustainable liquid for energy and carbon-based chemicals Green Chem. 2008, 10, 238-242
-
(2008)
Green Chem.
, vol.10
, pp. 238-242
-
-
Horváth, I.T.1
Mehdi, H.2
Fábos, V.3
Boda, L.4
Mika, L.T.5
-
5
-
-
79958847881
-
Searching for green solvents
-
Jessop, P. G. Searching for green solvents Green Chem. 2011, 13, 1391-1398
-
(2011)
Green Chem.
, vol.13
, pp. 1391-1398
-
-
Jessop, P.G.1
-
6
-
-
68849122570
-
Characterization of two lactones in liquid phase: An experimental and computational approach
-
Aparicio, S.; Alcalde, R. Characterization of two lactones in liquid phase: An experimental and computational approach Phys. Chem. Chem. Phys. 2009, 11, 6455-6467
-
(2009)
Phys. Chem. Chem. Phys.
, vol.11
, pp. 6455-6467
-
-
Aparicio, S.1
Alcalde, R.2
-
7
-
-
84907821002
-
-
4 th ed
-
Representatively, a dielectric constant of GVL at 25 °C is 36.47, which is important to compare dielectric constants for other polar aprotic solvents (25 °C): acetonitrile = 37.5, DMF = 36.7, NMP = 32.0, DMA = 37.8, taken from Vogels Textbook of Practical Organic Chemistry, 4 th ed.
-
Representatively, A Dielectric Constant of GVL at 25 °c is 36.47, Which is Important to Compare Dielectric Constants for Other Polar Aprotic Solvents (25 °c): Acetonitrile = 37.5, DMF = 36.7, NMP = 32.0, DMA = 37.8, Taken from Vogels Textbook of Practical Organic Chemistry
-
-
-
8
-
-
79953823038
-
Expanding GSKs solvent selection guide - Embedding sustainability into solvent selection starting at medicinal chemistry
-
Henderson, R. K.; Jimenez-Gonzalez, C.; Constable, D. J. C.; Alston, S. R.; Inglis, G. G. A.; Fisher, G.; Sherwood, J.; Binks, S. P.; Curzons, A. D. Expanding GSKs solvent selection guide-Embedding sustainability into solvent selection starting at medicinal chemistry Green Chem. 2011, 13, 854-862
-
(2011)
Green Chem.
, vol.13
, pp. 854-862
-
-
Henderson, R.K.1
Jimenez-Gonzalez, C.2
Constable, D.J.C.3
Alston, S.R.4
Inglis, G.G.A.5
Fisher, G.6
Sherwood, J.7
Binks, S.P.8
Curzons, A.D.9
-
9
-
-
34250862807
-
Key green chemistry research areas - A perspective from pharmaceutical manufacturers
-
Constable, D. J. C.; Dunn, P. J.; Hayler, J. D.; Humphrey, G. R.; Leazer, J. L.; Linderman, R. J., Jr.; Lorenz, K.; Manley, J.; Pearlman, B. A.; Wells, A.; Zaksh, A.; Zhang, T. Y. Key green chemistry research areas-A perspective from pharmaceutical manufacturers Green Chem. 2007, 9, 411-420
-
(2007)
Green Chem.
, vol.9
, pp. 411-420
-
-
Constable, D.J.C.1
Dunn, P.J.2
Hayler, J.D.3
Humphrey, G.R.4
Leazer, J.L.5
Linderman, R.J.6
Lorenz, K.7
Manley, J.8
Pearlman, B.A.9
Wells, A.10
Zaksh, A.11
Zhang, T.Y.12
-
10
-
-
84880836865
-
Palladium supported on cross-linked imidazolium network on silica as highly sustainable catalysts for the Suzuki reaction under flow conditions
-
As a representative example, see Pavia, C.; Ballerini, E.; Bivona, L. A.; Giacalone, F.; Aprile, C.; Vaccaro, L.; Gruttadauria, M. Palladium supported on cross-linked imidazolium network on silica as highly sustainable catalysts for the Suzuki reaction under flow conditions Adv. Synth. Catal. 2013, 355, 2007-2018
-
(2013)
Adv. Synth. Catal.
, vol.355
, pp. 2007-2018
-
-
Pavia, C.1
Ballerini, E.2
Bivona, L.A.3
Giacalone, F.4
Aprile, C.5
Vaccaro, L.6
Gruttadauria, M.7
-
11
-
-
84882588564
-
A waste-minimized protocol for the preparation of 1,2-azido alcohols and 1,2-amino alcohols
-
As a representative example, see Ballerini, E.; Crotti, P.; Frau, I.; Lanari, D.; Pizzo, F.; Vaccaro, L. A waste-minimized protocol for the preparation of 1,2-azido alcohols and 1,2-amino alcohols Green Chem. 2013, 15, 2394-2400
-
(2013)
Green Chem.
, vol.15
, pp. 2394-2400
-
-
Ballerini, E.1
Crotti, P.2
Frau, I.3
Lanari, D.4
Pizzo, F.5
Vaccaro, L.6
-
12
-
-
84904898536
-
Flow approaches towards sustainability
-
Vaccaro, L.; Lanari, D.; Marrocchi, A.; Strappaveccia, G. Flow approaches towards sustainability Green Chem. 2014, 16, 3680-3704
-
(2014)
Green Chem.
, vol.16
, pp. 3680-3704
-
-
Vaccaro, L.1
Lanari, D.2
Marrocchi, A.3
Strappaveccia, G.4
-
13
-
-
0036643495
-
How i came across the silicon-based cross-coupling reaction
-
Hiyama, T. How I came across the silicon-based cross-coupling reaction J. Organomet. Chem. 2002, 653, 58-61
-
(2002)
J. Organomet. Chem.
, vol.653
, pp. 58-61
-
-
Hiyama, T.1
-
14
-
-
57549105425
-
Palladium-catalyzed cross-coupling reactions of organosilanols and their salts: Practical alternatives to boron- and tin-based methods
-
Denmark, S. E.; Regens, C. S. Palladium-catalyzed cross-coupling reactions of organosilanols and their salts: practical alternatives to boron- and tin-based methods Acc. Chem. Res. 2008, 41, 1486-1499
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 1486-1499
-
-
Denmark, S.E.1
Regens, C.S.2
-
15
-
-
65249098596
-
The interplay of invention, discovery, development, and application in organic synthetic methodology: A case study
-
Denmark, S. E. The interplay of invention, discovery, development, and application in organic synthetic methodology: a case study J. Org. Chem. 2009, 74, 2915-2927
-
(2009)
J. Org. Chem.
, vol.74
, pp. 2915-2927
-
-
Denmark, S.E.1
-
16
-
-
77951169903
-
Silicon-based cross-coupling reactions in the total synthesis of natural products
-
Denmark, S. E.; Liu, J. H.-C. Silicon-based cross-coupling reactions in the total synthesis of natural products Angew. Chem., Int. Ed. 2010, 49, 2978-2986
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 2978-2986
-
-
Denmark, S.E.1
Liu, J.H.-C.2
-
17
-
-
77958068711
-
Recent advances in the use of temporary silicon tethers in metal-mediated reactions
-
Bracegirdle, S.; Anderson, E. A. Recent advances in the use of temporary silicon tethers in metal-mediated reactions Chem. Soc. Rev. 2010, 39, 4114-4129
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 4114-4129
-
-
Bracegirdle, S.1
Anderson, E.A.2
-
18
-
-
84856899190
-
Palladium-catalysed cross-coupling of organosilicon reagents
-
Sore, H. F.; Galloway, W. R. J. D.; Spring, D. R. Palladium-catalysed cross-coupling of organosilicon reagents Chem. Soc. Rev. 2012, 41, 1845-1866
-
(2012)
Chem. Soc. Rev.
, vol.41
, pp. 1845-1866
-
-
Sore, H.F.1
Galloway, W.R.J.D.2
Spring, D.R.3
-
19
-
-
80055021902
-
Silicon-based cross-coupling reaction: An environmentally benign version
-
Nakao, Y.; Hiyama, T. Silicon-based cross-coupling reaction: An environmentally benign version Chem. Soc. Rev. 2011, 40, 4893-4901
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 4893-4901
-
-
Nakao, Y.1
Hiyama, T.2
-
20
-
-
84900430396
-
Palladium-catalyzed cross-coupling reactions of arylsiloxanes with aryl halides: Application to solid-supported organic synthesis
-
Traficante, C. I.; Delpiccolo, C. M. L.; Mat, E. G. Palladium-catalyzed cross-coupling reactions of arylsiloxanes with aryl halides: Application to solid-supported organic synthesis ACS Comb. Sci. 2014, 16, 211-214
-
(2014)
ACS Comb. Sci.
, vol.16
, pp. 211-214
-
-
Traficante, C.I.1
Delpiccolo, C.M.L.2
Mat, E.G.3
-
21
-
-
84899433582
-
Efficient ligand-free Hiyama cross-coupling reaction catalyzed by functionalized SBA-15-supported Pd nanoparticles
-
Huang, S.-H.; Liu, C.-H.; Yang, C.-M. Efficient ligand-free Hiyama cross-coupling reaction catalyzed by functionalized SBA-15-supported Pd nanoparticles Green Chem. 2014, 16, 2706-2712
-
(2014)
Green Chem.
, vol.16
, pp. 2706-2712
-
-
Huang, S.-H.1
Liu, C.-H.2
Yang, C.-M.3
-
22
-
-
84879416709
-
Synthesis of substituted biaryls via Suzuki, Stille and Hiyama cross-coupling and homo-coupling reactions by CN-dimeric and monomeric ortho-palladated catalysts
-
Hajipoura, A. R.; Rafiee, F. Synthesis of substituted biaryls via Suzuki, Stille and Hiyama cross-coupling and homo-coupling reactions by CN-dimeric and monomeric ortho-palladated catalysts Appl. Organometal. Chem. 2013, 27, 412-418
-
(2013)
Appl. Organometal. Chem.
, vol.27
, pp. 412-418
-
-
Hajipoura, A.R.1
Rafiee, F.2
-
23
-
-
84878075120
-
Palladium-catalyzed Hiyama-type cross-coupling reactions of arenesulfinates with organosilanes
-
Cheng, K.; Hu, S.; Zhao, B.; Zhang, X.-M.; Qi, C. Palladium-catalyzed Hiyama-type cross-coupling reactions of arenesulfinates with organosilanes J. Org. Chem. 2013, 78, 5022-5025
-
(2013)
J. Org. Chem.
, vol.78
, pp. 5022-5025
-
-
Cheng, K.1
Hu, S.2
Zhao, B.3
Zhang, X.-M.4
Qi, C.5
-
24
-
-
84871614703
-
A practical protocol for the Hiyama cross-coupling reaction catalyzed by palladium on carbon
-
Monguchi, Y.; Yanase, T.; Mori, S.; Sajiki, H. A practical protocol for the Hiyama cross-coupling reaction catalyzed by palladium on carbon Synthesis 2013, 40-44
-
(2013)
Synthesis
, pp. 40-44
-
-
Monguchi, Y.1
Yanase, T.2
Mori, S.3
Sajiki, H.4
-
25
-
-
84870064436
-
A simple and efficient reusable polystyrene-supported palladium catalyst for Hiyama cross-coupling
-
Diebold, C.; Derible, A.; Becht, J.-M.; Le Drian, C. A simple and efficient reusable polystyrene-supported palladium catalyst for Hiyama cross-coupling Tetrahedron 2013, 69, 264-267
-
(2013)
Tetrahedron
, vol.69
, pp. 264-267
-
-
Diebold, C.1
Derible, A.2
Becht, J.-M.3
Le Drian, C.4
-
26
-
-
84856405117
-
Application of a dimeric ortho-palladated complex of tribenzylamine as an efficient catalyst in microwave-assisted Hiyama coupling reactions
-
Hajipoura, A. R.; Rafiee, F. Application of a dimeric ortho-palladated complex of tribenzylamine as an efficient catalyst in microwave-assisted Hiyama coupling reactions Appl. Organometal. Chem. 2012, 26, 51-55
-
(2012)
Appl. Organometal. Chem.
, vol.26
, pp. 51-55
-
-
Hajipoura, A.R.1
Rafiee, F.2
-
27
-
-
84859146379
-
Ligand-free Hiyama cross-coupling reaction catalyzed by palladium on carbon
-
Yanase, T.; Monguchi, Y.; Sajiki, H. Ligand-free Hiyama cross-coupling reaction catalyzed by palladium on carbon RSC Adv. 2012, 2, 590-594
-
(2012)
RSC Adv.
, vol.2
, pp. 590-594
-
-
Yanase, T.1
Monguchi, Y.2
Sajiki, H.3
-
28
-
-
67650499640
-
Palladium-catalysed synthesis of aryl-alkyl ethers using alkoxysilanes as nucleophiles
-
Milton, E. J.; Fuentes, J. A.; Clarke, M. L. Palladium-catalysed synthesis of aryl-alkyl ethers using alkoxysilanes as nucleophiles Org. Biomol. Chem. 2009, 7, 2645-2648
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 2645-2648
-
-
Milton, E.J.1
Fuentes, J.A.2
Clarke, M.L.3
-
29
-
-
61449107642
-
Palladium-indolylphosphine-catalyzed Hiyama cross-coupling of aryl mesylates
-
So, C. M.; Lee, H. W.; Lau, C. P.; Kwong, F. Y. Palladium-indolylphosphine-catalyzed Hiyama cross-coupling of aryl mesylates Org. Lett. 2009, 11, 317-320
-
(2009)
Org. Lett.
, vol.11
, pp. 317-320
-
-
So, C.M.1
Lee, H.W.2
Lau, C.P.3
Kwong, F.Y.4
-
30
-
-
33645017030
-
Cross-coupling reactions of aryl and vinyl chlorides catalyzed by a palladium complex derived from an air-stable H-phosphonate
-
Ackermann, L.; Gschrei, C. J.; Althammer, A.; Riederer, M. Cross-coupling reactions of aryl and vinyl chlorides catalyzed by a palladium complex derived from an air-stable H-phosphonate Chem. Commun. 2006, 1419-1421
-
(2006)
Chem. Commun.
, pp. 1419-1421
-
-
Ackermann, L.1
Gschrei, C.J.2
Althammer, A.3
Riederer, M.4
-
31
-
-
84897026350
-
Hiyama cross-coupling reaction catalyzed by a palladium salt of 1-benzyl-4-aza-1-azoniabicyclo [2.2.2]octane chloride under microwave irradiation
-
Hajipoura, A. R.; Rafiee, F.; Najafi, N. Hiyama cross-coupling reaction catalyzed by a palladium salt of 1-benzyl-4-aza-1-azoniabicyclo [2.2.2]octane chloride under microwave irradiation Appl. Organometal. Chem. 2014, 28, 217-220
-
(2014)
Appl. Organometal. Chem.
, vol.28
, pp. 217-220
-
-
Hajipoura, A.R.1
Rafiee, F.2
Najafi, N.3
-
32
-
-
84886257575
-
Copper-catalyzed Hiyama coupling of (hetero)aryltriethoxysilanes with (hetero)aryl iodides
-
Gurung, S. K.; Thapa, S.; Vangala, A. S.; Giri, R. Copper-catalyzed Hiyama coupling of (hetero)aryltriethoxysilanes with (hetero)aryl iodides Org. Lett. 2013, 15, 5378-5381
-
(2013)
Org. Lett.
, vol.15
, pp. 5378-5381
-
-
Gurung, S.K.1
Thapa, S.2
Vangala, A.S.3
Giri, R.4
-
33
-
-
84877051038
-
Supported palladium nanoparticles as heterogeneous ligand-free catalysts for the Hiyama C-C coupling of vinylsilanes and halobenzenes leading to styrenes
-
Grirrane, A.; Garcia, H.; Corma, A. Supported palladium nanoparticles as heterogeneous ligand-free catalysts for the Hiyama C-C coupling of vinylsilanes and halobenzenes leading to styrenes J. Catal. 2013, 302, 49-57
-
(2013)
J. Catal.
, vol.302
, pp. 49-57
-
-
Grirrane, A.1
Garcia, H.2
Corma, A.3
-
34
-
-
84896735837
-
1,2-Functionalized imidazoles as palladium ligands: An efficient and robust catalytic system for the fluorine-free Hiyama reaction
-
Martínez, R.; Pastor, I. M.; Yus, M. 1,2-Functionalized imidazoles as palladium ligands: an efficient and robust catalytic system for the fluorine-free Hiyama reaction Eur. J. Org. Chem. 2014, 872-877
-
(2014)
Eur. J. Org. Chem.
, pp. 872-877
-
-
Martínez, R.1
Pastor, I.M.2
Yus, M.3
-
35
-
-
84907852518
-
Microwave assisted fluoride-free Hiyama cross-coupling reaction catalyzed by Pd (0)-PVP nanoparticles
-
Shah, D.; Kaur, H. Microwave assisted fluoride-free Hiyama cross-coupling reaction catalyzed by Pd (0)-PVP nanoparticles Curr. Catal. 2014, 3, 39-46
-
(2014)
Curr. Catal.
, vol.3
, pp. 39-46
-
-
Shah, D.1
Kaur, H.2
-
36
-
-
84884484235
-
Mechanistic studies on the Pd-catalyzed vinylation of aryl halides with vinylalkoxysilanes in water: The effect of the solvent and NaOH promoter
-
Gordillo, A.; Ortuño, M. A.; López-Mardomingo, C.; Lledós, A.; Ujaque, G.; de Jesús, E. Mechanistic studies on the Pd-catalyzed vinylation of aryl halides with vinylalkoxysilanes in water: The effect of the solvent and NaOH promoter J. Am. Chem. Soc. 2013, 135, 13749-13763
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 13749-13763
-
-
Gordillo, A.1
Ortuño, M.A.2
López-Mardomingo, C.3
Lledós, A.4
Ujaque, G.5
De Jesús, E.6
-
37
-
-
33744814897
-
Solvent-less and fluoride-free Hiyama reaction of arylsiloxanes with aryl bromides and chlorides promoted by sodium hydroxide: A useful protocol for palladium recycling and product isolation
-
Alacida, E.; Najera, C. Solvent-less and fluoride-free Hiyama reaction of arylsiloxanes with aryl bromides and chlorides promoted by sodium hydroxide: A useful protocol for palladium recycling and product isolation Adv. Synth. Catal. 2006, 348, 945-952
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 945-952
-
-
Alacida, E.1
Najera, C.2
-
38
-
-
33750494972
-
The first fluoride-free Hiyama reaction of vinylsiloxanes promoted by sodium hydroxide in water
-
Alacida, E.; Najera, C. The first fluoride-free Hiyama reaction of vinylsiloxanes promoted by sodium hydroxide in water Adv. Synth. Catal. 2006, 348, 2085-2091
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 2085-2091
-
-
Alacida, E.1
Najera, C.2
-
39
-
-
82255178998
-
Improved Hiyama cross-coupling reactions using HOMSi® reagents: A novel application of a palladacycle
-
Marcuccio, S. M.; Epa, R.; Moslmani, M.; Hughes, A. B. Improved Hiyama cross-coupling reactions using HOMSi® reagents: A novel application of a palladacycle Tetrahedron Lett. 2011, 52, 7178-7181
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 7178-7181
-
-
Marcuccio, S.M.1
Epa, R.2
Moslmani, M.3
Hughes, A.B.4
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