Výsledky vyhledávání

Akademický článek

Homogeneous Organic Reductant Based on 4,4'- ^t Bu 2 -2,2'-Bipyridine for Cross-Electrophile Coupling.

Autor: Charboneau DJ; Department of Chemistry, Yale University, P. O. Box 208107, New Haven, Connecticut, 06520, USA., Huang H; Department of Chemistry, Yale University, P. O. Box 208107, New Haven, Connecticut, 06520, USA., Barth EL; Department of Chemistry, Yale University, P. O. Box 208107, New Haven, Connecticut, 06520, USA., Deziel AP; Department of Chemistry, Yale University, P. O. Box 208107, New Haven, Connecticut, 06520, USA., Germe CC; Department of Chemistry, Yale University, P. O. Box 208107, New Haven, Connecticut, 06520, USA., Hazari N; Department of Chemistry, Yale University, P. O. Box 208107, New Haven, Connecticut, 06520, USA., Jia X; Department of Chemistry, Yale University, P. O. Box 208107, New Haven, Connecticut, 06520, USA., Kim S; Department of Chemistry, Yale University, P. O. Box 208107, New Haven, Connecticut, 06520, USA., Nahiyan S; Department of Chemistry, Yale University, P. O. Box 208107, New Haven, Connecticut, 06520, USA., Birriel-Rodriguez L; Department of Chemistry, Yale University, P. O. Box 208107, New Haven, Connecticut, 06520, USA., Uehling MR; Merck & Co., Inc., Discovery Chemistry, HTE and Lead Discovery Capabilities, Rahway, New Jersey, 07065, USA.

Publikováno v: Tetrahedron letters [Tetrahedron Lett] 2024 Jul 28; Vol. 145. Date of Electronic Publication: 2024 Jun 19.

Zobrazit plný text záznamu

Akademický článek

Stimuli-Modulated Metal Oxidation States in Photochromic MOFs.

Autor: Martin CR; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States., Park KC; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States., Leith GA; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States., Yu J; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States., Mathur A; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States., Wilson GR; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States., Gange GB; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States., Barth EL; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Ly RT; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States., Manley OM; Department of Chemistry, North Carolina State University, 2620 Yarbrough Drive, Raleigh, North Carolina 27695, United States., Forrester KL; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States., Karakalos SG; College of Engineering and Computing, University of South Carolina, Columbia, South Carolina 29208, United States., Smith MD; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States., Makris TM; Department of Chemistry, North Carolina State University, 2620 Yarbrough Drive, Raleigh, North Carolina 27695, United States., Vannucci AK; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States., Peryshkov DV; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States., Shustova NB; Department of Chemistry and Biochemistry, University of South Carolina, 631 Sumter Street, Columbia, South Carolina 29208, United States.

Publikováno v: Journal of the American Chemical Society [J Am Chem Soc] 2022 Mar 16; Vol. 144 (10), pp. 4457-4468. Date of Electronic Publication: 2022 Feb 09.

Zobrazit plný text záznamu

Akademický článek

Tunable and Practical Homogeneous Organic Reductants for Cross-Electrophile Coupling.

Autor: Charboneau DJ; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Huang H; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Barth EL; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Germe CC; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Hazari N; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Mercado BQ; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Uehling MR; Discovery Chemistry, HTE and Lead Discovery Capabilities, Merck & Co., Inc., Kenilworth, New Jersey 07033, United States., Zultanski SL; Department of Process Research and Development, Merck & Co., Inc., Kenilworth, New Jersey 07033, United States.

Publikováno v: Journal of the American Chemical Society [J Am Chem Soc] 2021 Dec 15; Vol. 143 (49), pp. 21024-21036. Date of Electronic Publication: 2021 Nov 30.

Zobrazit plný text záznamu

Akademický článek

A Widely Applicable Dual Catalytic System for Cross-Electrophile Coupling Enabled by Mechanistic Studies.

Autor: Charboneau DJ; Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States., Barth EL; Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States., Hazari N; Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States., Uehling MR; Merck & Co., Inc., Discovery Chemistry, HTE and Lead Discovery Capabilities, Kenilworth, New Jersey 07033, United States., Zultanski SL; Merck & Co., Inc., Department of Process Research and Development, Rahway, New Jersey 07065, United States.

Publikováno v: ACS catalysis [ACS Catal] 2020 Nov 06; Vol. 10 (21), pp. 12642-12656. Date of Electronic Publication: 2020 Sep 29.

Zobrazit plný text záznamu

Akademický článek

Bis(dialkylphosphino)ferrocene-Ligated Nickel(II) Precatalysts for Suzuki-Miyaura Reactions of Aryl Carbonates.

Autor: Barth EL; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Davis RM; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Beromi MM; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Walden AG; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Balcells D; Hylleraas Centre for Quantum Molecular Sciences, Department of Chemistry, University of Oslo, P.O. Box 1033, Blindern, N-0315 Oslo, Norway., Brudvig GW; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Dardir AH; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Hazari N; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Lant HMC; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Mercado BQ; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States., Peczak IL; Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States.

Publikováno v: Organometallics [Organometallics] 2019 Sep 09; Vol. 38 (17), pp. 3377-3387. Date of Electronic Publication: 2019 Aug 26.

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání