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Ligand Effects on the Stereochemical Outcome of Suzuki–Miyaura Couplings

Journal of organic chemistry, 2012-04, Vol.77 (8), p.3700-3703

2012

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Ligand effects on the stereochemistry of Stille couplings, as manifested in reactions of Z-alkenyl halides

Chemical communications (Cambridge, England), 2012-01, Vol.48 (69), p.8661-8663

2012

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Regioselective reductions of β,β-disubstituted enones catalyzed by nonracemically ligated copper hydride

Tetrahedron, 2012-04, Vol.68 (17), p.3410-3416

2012

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ML418: The First Selective, Sub-Micromolar Pore Blocker of Kir7.1 Potassium Channels

ACS chemical neuroscience, 2016-07, Vol.7 (7), p.1013-1023

2016

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Miyaura Borylations of Aryl Bromides in Water at Room Temperature

Israel journal of chemistry, 2010-12, Vol.50 (5-6), p.691-695

2010

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Rearrangements of Allylic Sulfinates to Sulfones: A Mechanistic Study

Journal of chemical education, 2010-07, Vol.87 (7), p.717-720

2010

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Ligand effects on the stereochemistry of Stille couplings, as manifested in reactions of Z-alkenyl halidesElectronic supplementary information (ESI) available: Experimental details and characterization data of all products. See DOI: 10.1039/c2cc33294a

2012-08

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Regioselective reductions of β,β-disubstituted enones catalyzed by nonracemically ligated copper hydride: Symposium-in-Print 157: New Trends in Enantioselective Catalysis with Copper (I)

Tetrahedron, 2012, Vol.68 (17)

2012

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ChemInform Abstract: Ligand Effects on the Stereochemistry of Stille Couplings, as Manifested in Reactions of (Z)-Alkenyl Halides

ChemInform, 2012-12, Vol.43 (50), p.no-no

2012

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ChemInform Abstract: Ligand Effects on the Stereochemical Outcome of Suzuki-Miyaura Couplings

ChemInform, 2012-08, Vol.43 (33), p.no-no

2012

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ChemInform Abstract: Regioselective Reductions of β,β-Disubstituted Enones Catalyzed by Nonracemically Ligated Copper Hydride

ChemInform, 2012-10, Vol.43 (44), p.no-no

2012

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ChemInform Abstract: Regioselective Reductions of [beta],[beta]-Disubstituted Enones Catalyzed by Nonracemically Ligated Copper Hydride

ChemInform, 2012-10, Vol.43 (44), p.no

2012

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ChemInform Abstract: Asymmetric CuH-Catalyzed 1,4-Reductions in Water at Room Temperature

ChemInform, 2010-11, Vol.41 (48), p.no-no

2010

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Ligand Effects on the Stereochemical Outcome of Suzuki–Miyaura Couplings

Ligand effects on the stereochemistry of Stille couplings, as manifested in reactions of Z-alkenyl halides

Regioselective reductions of β,β-disubstituted enones catalyzed by nonracemically ligated copper hydride

ML418: The First Selective, Sub-Micromolar Pore Blocker of Kir7.1 Potassium Channels

Miyaura Borylations of Aryl Bromides in Water at Room Temperature

Rearrangements of Allylic Sulfinates to Sulfones: A Mechanistic Study

Ligand effects on the stereochemistry of Stille couplings, as manifested in reactions of Z-alkenyl halidesElectronic supplementary information (ESI) available: Experimental details and characterization data of all products. See DOI: 10.1039/c2cc33294a

Regioselective reductions of β,β-disubstituted enones catalyzed by nonracemically ligated copper hydride: Symposium-in-Print 157: New Trends in Enantioselective Catalysis with Copper (I)

ChemInform Abstract: Ligand Effects on the Stereochemistry of Stille Couplings, as Manifested in Reactions of (Z)-Alkenyl Halides

ChemInform Abstract: Ligand Effects on the Stereochemical Outcome of Suzuki-Miyaura Couplings

ChemInform Abstract: Regioselective Reductions of β,β-Disubstituted Enones Catalyzed by Nonracemically Ligated Copper Hydride

ChemInform Abstract: Regioselective Reductions of [beta],[beta]-Disubstituted Enones Catalyzed by Nonracemically Ligated Copper Hydride

ChemInform Abstract: Asymmetric CuH-Catalyzed 1,4-Reductions in Water at Room Temperature

Discovery and Optimization of Potent and CNS Penetrant M 5 -Preferring Positive Allosteric Modulators Derived from a Novel, Chiral N-(Indanyl)piperidine Amide Scaffold

Discovery and Optimization of Potent and CNS Penetrant M5‑Preferring Positive Allosteric Modulators Derived from a Novel, Chiral N‑(Indanyl)piperidine Amide Scaffold

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