Monfette S - Search Results

1

Parallel multi-droplet platform for reaction kinetics and optimization.

Eyke NS, Schneider TN, Jin B, Hart T, Monfette S, Hawkins JM, Morse PD, Howard RM, Pfisterer DM, Nandiwale KY, Jensen KF. Eyke NS, et al. Among authors: monfette s. Chem Sci. 2023 Aug 4;14(33):8798-8809. doi: 10.1039/d3sc02082g. eCollection 2023 Aug 23. Chem Sci. 2023. PMID: 37621435 Free PMC article.

2

Keeping an "eye" on the experiment: computer vision for real-time monitoring and control.

El-Khawaldeh R, Guy M, Bork F, Taherimakhsousi N, Jones KN, Hawkins JM, Han L, Pritchard RP, Cole BA, Monfette S, Hein JE. El-Khawaldeh R, et al. Among authors: monfette s. Chem Sci. 2023 Nov 27;15(4):1271-1282. doi: 10.1039/d3sc05491h. eCollection 2024 Jan 24. Chem Sci. 2023. PMID: 38274057 Free PMC article.

3

Enabling Suzuki-Miyaura coupling of Lewis-basic arylboronic esters with a nonprecious metal catalyst.

Haibach MC, Ickes AR, Tcyrulnikov S, Shekhar S, Monfette S, Swiatowiec R, Kotecki BJ, Wang J, Wall AL, Henry RF, Hansen EC. Haibach MC, et al. Among authors: monfette s. Chem Sci. 2022 Oct 21;13(43):12906-12912. doi: 10.1039/d2sc03877c. eCollection 2022 Nov 9. Chem Sci. 2022. PMID: 36519062 Free PMC article.

4

Computationally Guided Ligand Discovery from Compound Libraries and Discovery of a New Class of Ligands for Ni-Catalyzed Cross-Electrophile Coupling of Challenging Quinoline Halides.

Tcyrulnikov S, Hubbell AK, Pedro D, Reyes GP, Monfette S, Weix DJ, Hansen EC. Tcyrulnikov S, et al. Among authors: monfette s. J Am Chem Soc. 2024 Mar 13;146(10):6947-6954. doi: 10.1021/jacs.3c14607. Epub 2024 Mar 1. J Am Chem Soc. 2024. PMID: 38427582

5

Computational Methods Enable the Prediction of Improved Catalysts for Nickel-Catalyzed Cross-Electrophile Coupling.

Akana ME, Tcyrulnikov S, Akana-Schneider BD, Reyes GP, Monfette S, Sigman MS, Hansen EC, Weix DJ. Akana ME, et al. Among authors: monfette s. J Am Chem Soc. 2024 Feb 7;146(5):3043-3051. doi: 10.1021/jacs.3c09554. Epub 2024 Jan 26. J Am Chem Soc. 2024. PMID: 38276910

6

A Ru-isocyanate initiator for fast, living, precisely controlled ring-opening metathesis polymerization at ambient temperatures.

Monfette S, Marleau-Gillette J, Conrad JC, McDonald R, Fogg DE. Monfette S, et al. Dalton Trans. 2012 Dec 28;41(48):14476-9. doi: 10.1039/c2dt32568c. Dalton Trans. 2012. PMID: 23135064

7

Enantiopure C1-symmetric bis(imino)pyridine cobalt complexes for asymmetric alkene hydrogenation.

Monfette S, Turner ZR, Semproni SP, Chirik PJ. Monfette S, et al. J Am Chem Soc. 2012 Mar 14;134(10):4561-4. doi: 10.1021/ja300503k. Epub 2012 Mar 6. J Am Chem Soc. 2012. PMID: 22390262

8

Getting ring-closing metathesis off the bench: reaction-reactor matching transforms metathesis efficiency in the assembly of large rings.

Monfette S, Eyholzer M, Roberge DM, Fogg DE. Monfette S, et al. Chemistry. 2010 Oct 11;16(38):11720-5. doi: 10.1002/chem.201001210. Epub 2010 Sep 6. Chemistry. 2010. PMID: 20821763

9

Equilibrium ring-closing metathesis.

Monfette S, Fogg DE. Monfette S, et al. Chem Rev. 2009 Aug;109(8):3783-816. doi: 10.1021/cr800541y. Chem Rev. 2009. PMID: 19537778 No abstract available.

10

Oligomers as intermediates in ring-closing metathesis.

Conrad JC, Eelman MD, Silva JA, Monfette S, Parnas HH, Snelgrove JL, Fogg DE. Conrad JC, et al. Among authors: monfette s. J Am Chem Soc. 2007 Feb 7;129(5):1024-5. doi: 10.1021/ja067531t. J Am Chem Soc. 2007. PMID: 17263371 No abstract available.

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