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Items: 1 to 20 of 68

1.

Dual Roles for Potassium Hydride in Haloarene Reduction: CSNAr and Single Electron Transfer Reduction via Organic Electron Donors Formed in Benzene.

Barham JP, Dalton SE, Allison M, Nocera G, Young A, John MP, McGuire T, Campos S, Tuttle T, Murphy JA.

J Am Chem Soc. 2018 Sep 12;140(36):11510-11518. doi: 10.1021/jacs.8b07632. Epub 2018 Aug 30.

PMID:
30119605
2.

New Insights into the Catalytic Mechanism of Aldose Reductase: A QM/MM Study.

Dréanic MP, Edge CM, Tuttle T.

ACS Omega. 2017 Sep 30;2(9):5737-5747. doi: 10.1021/acsomega.7b00815. Epub 2017 Sep 14.

3.

Electron Transfer Reactions: KO tBu (but not NaO tBu) Photoreduces Benzophenone under Activation by Visible Light.

Nocera G, Young A, Palumbo F, Emery KJ, Coulthard G, McGuire T, Tuttle T, Murphy JA.

J Am Chem Soc. 2018 Aug 1;140(30):9751-9757. doi: 10.1021/jacs.8b06089. Epub 2018 Jul 24.

PMID:
29996048
4.

KOtBu as a Single Electron Donor? Revisiting the Halogenation of Alkanes with CBr₄ and CCl₄.

Emery KJ, Young A, Arokianathar JN, Tuttle T, Murphy JA.

Molecules. 2018 May 1;23(5). pii: E1055. doi: 10.3390/molecules23051055.

5.

Evidence of single electron transfer from the enolate anion of an N,N'-dialkyldiketopiperazine additive in BHAS coupling reactions.

Emery KJ, Tuttle T, Murphy JA.

Org Biomol Chem. 2017 Oct 25;15(41):8810-8819. doi: 10.1039/c7ob02209c.

PMID:
29022630
6.

Electron-Transfer and Hydride-Transfer Pathways in the Stoltz-Grubbs Reducing System (KOtBu/Et3 SiH).

Smith AJ, Young A, Rohrbach S, O'Connor EF, Allison M, Wang HS, Poole DL, Tuttle T, Murphy JA.

Angew Chem Int Ed Engl. 2017 Oct 23;56(44):13747-13751. doi: 10.1002/anie.201707914. Epub 2017 Oct 2.

7.

Cooperative, ion-sensitive co-assembly of tripeptide hydrogels.

Abul-Haija YM, Scott GG, Sahoo JK, Tuttle T, Ulijn RV.

Chem Commun (Camb). 2017 Aug 24;53(69):9562-9565. doi: 10.1039/c7cc04796g.

PMID:
28805225
8.

Polymeric peptide pigments with sequence-encoded properties.

Lampel A, McPhee SA, Park HA, Scott GG, Humagain S, Hekstra DR, Yoo B, Frederix PWJM, Li TD, Abzalimov RR, Greenbaum SG, Tuttle T, Hu C, Bettinger CJ, Ulijn RV.

Science. 2017 Jun 9;356(6342):1064-1068. doi: 10.1126/science.aal5005.

PMID:
28596363
9.

Iridium-Catalyzed Formyl-Selective Deuteration of Aldehydes.

Kerr WJ, Reid M, Tuttle T.

Angew Chem Int Ed Engl. 2017 Jun 26;56(27):7808-7812. doi: 10.1002/anie.201702997. Epub 2017 Jun 7.

PMID:
28510987
10.

Biocatalytic Self-Assembly of Tripeptide Gels and Emulsions.

Moreira IP, Piskorz TK, van Esch JH, Tuttle T, Ulijn RV.

Langmuir. 2017 May 23;33(20):4986-4995. doi: 10.1021/acs.langmuir.7b00428. Epub 2017 May 12.

PMID:
28463516
11.

A study of diketopiperazines as electron-donor initiators in transition metal-free haloarene-arene coupling.

Cumine F, Zhou S, Tuttle T, Murphy JA.

Org Biomol Chem. 2017 Apr 11;15(15):3324-3336. doi: 10.1039/c7ob00036g.

PMID:
28362016
12.

An Ambipolar BODIPY Derivative for a White Exciplex OLED and Cholesteric Liquid Crystal Laser toward Multifunctional Devices.

Chapran M, Angioni E, Findlay NJ, Breig B, Cherpak V, Stakhira P, Tuttle T, Volyniuk D, Grazulevicius JV, Nastishin YA, Lavrentovich OD, Skabara PJ.

ACS Appl Mater Interfaces. 2017 Feb 8;9(5):4750-4757. doi: 10.1021/acsami.6b13689. Epub 2017 Jan 24.

13.

Effect of solvent on radical cyclisation pathways: SRN1 vs. aryl-aryl bond forming mechanisms.

Emery KJ, Murphy JA, Tuttle T.

Org Biomol Chem. 2017 Jan 25;15(4):920-927. doi: 10.1039/c6ob02684b.

PMID:
28050609
14.

KOtBu: A Privileged Reagent for Electron Transfer Reactions?

Barham JP, Coulthard G, Emery KJ, Doni E, Cumine F, Nocera G, John MP, Berlouis LE, McGuire T, Tuttle T, Murphy JA.

J Am Chem Soc. 2016 Jun 15;138(23):7402-10. doi: 10.1021/jacs.6b03282. Epub 2016 May 26.

15.

Enzymatically activated emulsions stabilised by interfacial nanofibre networks.

Moreira IP, Sasselli IR, Cannon DA, Hughes M, Lamprou DA, Tuttle T, Ulijn RV.

Soft Matter. 2016 Mar 7;12(9):2623-31. doi: 10.1039/c5sm02730f. Epub 2016 Feb 1.

PMID:
26905042
16.

Supramolecular Fibers in Gels Can Be at Thermodynamic Equilibrium: A Simple Packing Model Reveals Preferential Fibril Formation versus Crystallization.

Sasselli IR, Halling PJ, Ulijn RV, Tuttle T.

ACS Nano. 2016 Feb 23;10(2):2661-8. doi: 10.1021/acsnano.5b07690. Epub 2016 Jan 29.

PMID:
26812130
17.

Influence of Solvent in Controlling Peptide-Surface Interactions.

Cannon DA, Ashkenasy N, Tuttle T.

J Phys Chem Lett. 2015 Oct 1;6(19):3944-9. doi: 10.1021/acs.jpclett.5b01733. Epub 2015 Sep 18.

PMID:
26722896
18.

Tripeptide Emulsifiers.

Scott GG, McKnight PJ, Tuttle T, Ulijn RV.

Adv Mater. 2016 Feb 17;28(7):1381-6. doi: 10.1002/adma.201504697. Epub 2015 Dec 7.

PMID:
26639675
19.

Thiazole-induced rigidification in substituted dithieno-tetrathiafulvalene: the effect of planarisation on charge transport properties.

Taylor RG, Cameron J, Wright IA, Thomson N, Avramchenko O, Kanibolotsky AL, Inigo AR, Tuttle T, Skabara PJ.

Beilstein J Org Chem. 2015 Jul 10;11:1148-54. doi: 10.3762/bjoc.11.129. eCollection 2015.

20.

Iridium-Catalysed ortho-Directed Deuterium Labelling of Aromatic Esters--An Experimental and Theoretical Study on Directing Group Chemoselectivity.

Devlin J, Kerr WJ, Lindsay DM, McCabe TJ, Reid M, Tuttle T.

Molecules. 2015 Jun 25;20(7):11676-98. doi: 10.3390/molecules200711676.

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