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Items: 1 to 20 of 82

1.

How does aqueous solubility of organic reactant affect a water-promoted reaction?

Zuo YJ, Qu J.

J Org Chem. 2014 Aug 1;79(15):6832-9. doi: 10.1021/jo500733v. Epub 2014 Jul 16.

PMID:
25000435
2.

Invoking pairwise interactions in water-promoted Diels-Alder reactions by using ionic liquids as cosolvents.

Manna A, Kumar A.

Chemphyschem. 2014 Oct 6;15(14):3067-77. doi: 10.1002/cphc.201402338. Epub 2014 Jul 25.

PMID:
25065603
3.

Use of different types of mesoporous materials as tools for organic synthesis.

Witula T, Holmberg K.

J Colloid Interface Sci. 2007 Jun 15;310(2):536-45. Epub 2007 Feb 27.

PMID:
17328906
5.
6.

Solubility of hydrophobic organic pollutants in binary and multicomponent aqueous solvents.

Ruckenstein E, Shulgin I.

Environ Sci Technol. 2005 Mar 15;39(6):1623-31.

PMID:
15819218
8.

Organic chemistry of graphene: the Diels-Alder reaction.

Denis PA.

Chemistry. 2013 Nov 11;19(46):15719-25. doi: 10.1002/chem.201302622. Epub 2013 Oct 2.

PMID:
24115199
9.

Suzuki coupling reactions in neat water as the solvent: where in the biphasic reaction mixture do the catalytic reaction steps occur?

Röhlich C, Wirth AS, Köhler K.

Chemistry. 2012 Nov 26;18(48):15485-94. doi: 10.1002/chem.201201266. Epub 2012 Oct 2.

PMID:
23032729
10.

Vinylboronic Acids as Fast Reacting, Synthetically Accessible, and Stable Bioorthogonal Reactants in the Carboni-Lindsey Reaction.

Eising S, Lelivelt F, Bonger KM.

Angew Chem Int Ed Engl. 2016 Sep 26;55(40):12243-7. doi: 10.1002/anie.201605271. Epub 2016 Sep 8.

11.
12.

Cyclodextrin-promoted Diels Alder reactions of a polycyclic aromatic hydrocarbon under mild reaction conditions.

Chaudhuri S, Phelan T, Levine M.

Tetrahedron Lett. 2015 Mar 1;56(13):1619-1623. Epub 2015 Feb 9.

13.

Accelerating the "On Water" Reaction: By Organic-Water Interface or By Hydrodynamic Effects?

Guo D, Zhu D, Zhou X, Zheng B.

Langmuir. 2015 Dec 29;31(51):13759-63. doi: 10.1021/acs.langmuir.5b04031. Epub 2015 Dec 16.

PMID:
26624935
14.

A lipid-coated lipase as an efficient hydrolytic catalyst in the two-phase aqueous-organic system.

Mori T, Kishimoto S, Ijiro K, Kobayashi A, Okahata Y.

Biotechnol Bioeng. 2001 Sep;76(2):157-63.

PMID:
11505385
15.

Diels-Alder reactions of 3-substituted coumarins in water and under high-pressure condition. An uncatalyzed route to tetrahydro-6H-benzo[c]chromen-6-ones.

Girotti R, Marrocchi A, Minuti L, Piermatti O, Pizzo F, Vaccaro L.

J Org Chem. 2006 Jan 6;71(1):70-4.

PMID:
16388619
16.

Acceleration of disproportionation of aromatic alcohols through self-emulsification of reactants in water.

Zhang B, Song J, Liu H, Han B, Jiang T, Fan H, Zhang Z, Wu T.

ChemSusChem. 2012 Dec;5(12):2469-73. doi: 10.1002/cssc.201200562. Epub 2012 Oct 22.

PMID:
23090937
17.
18.

The use of hydrophilic groups in aqueous organic reactions.

Itami K, Yoshida J.

Chem Rec. 2002;2(4):213-24. Review.

PMID:
12203904
19.

Effect of a microemulsion system on hapten-peptide reactivity studies: examples of hydroxycitronellal and citral, fragrance skin sensitizers, with glutathione.

Merckel F, Bernard G, Mutschler J, Giménez-Arnau E, Gerberick GF, Lepoittevin JP.

Chem Res Toxicol. 2010 Sep 20;23(9):1433-41. doi: 10.1021/tx100043b.

PMID:
20795681
20.

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