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One-pot palladium-catalyzed synthesis of sulfonyl fluorides from aryl bromides

Chemical science (Cambridge), 2017, Vol.8 (2), p.1233-1237

2017

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Mild Aromatic Palladium-Catalyzed Protodecarboxylation: Kinetic Assessment of the Decarboxylative Palladation and the Protodepalladation Steps

Journal of organic chemistry, 2013-05, Vol.78 (10), p.4744-4761

2013

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Chemoselective activation of sp(3) vs sp(2) C-H bonds with Pd(II)

Journal of the American Chemical Society, 2015-01, Vol.137 (1), p.18-21

2015

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Palladium-Catalyzed Chemoselective Activation of sp3 vs sp2 C–H Bonds: Oxidative Coupling To Form Quaternary Centers

ACS catalysis, 2019-04, Vol.9 (4), p.3716-3724

2019

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A General Synthesis of Dihydronaphthyridinones with Aryl-Substituted Quaternary Benzylic Centers

Journal of organic chemistry, 2023-03, Vol.88 (5), p.3340-3345

2023

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One-Step Synthesis of Sulfonamides from N‑Tosylhydrazones

Organic letters, 2016-02, Vol.18 (3), p.508-511

2016

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A Small-Molecule Oral Agonist of the Human Glucagon-like Peptide‑1 Receptor

Journal of medicinal chemistry, 2022-06, Vol.65 (12), p.8208-8226

2022

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Preparation of Azinones from (Cyclopropylmethoxy)azine Ethers

Journal of organic chemistry, 2023-05, Vol.88 (9), p.5671-5675

2023

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Asymmetric Synthesis of α‑Allyl-α-Aryl α‑Amino Acids by Tandem Alkylation/π-Allylation of α‑Iminoesters

Organic letters, 2014-04, Vol.16 (7), p.1948-1951

2014

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Lewis Acid-Promoted Enantioselective Dearomative Spirocyclizations of Allenes

Journal of organic chemistry, 2018-10, Vol.83 (19), p.12207-12212

2018

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α‑Allyl-α-aryl α‑Amino Esters in the Asymmetric Synthesis of Acyclic and Cyclic Amino Acid Derivatives by Alkene Metathesis

Journal of organic chemistry, 2014-06, Vol.79 (11), p.5359-5364

2014

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6-Azaspiro[2.5]octanes as small molecule agonists of the human glucagon-like peptide-1 receptor

Bioorganic & medicinal chemistry letters, 2023-10, Vol.94, p.129454-129454, Article 129454

2023

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Chemoselective Activation of sp3 vs sp2 C–H Bonds with Pd(II)

Journal of the American Chemical Society, 2014-11, Vol.137 (1), p.18-21

2014

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Support of academic synthetic chemistry using separation technologies from the pharmaceutical industry

Organic & biomolecular chemistry, 2014-04, Vol.12 (14), p.2161-2166

2014

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Palladium-Catalyzed Chemoselective Activation of sp 3 vs sp 2 C-H Bonds: Oxidative Coupling To Form Quaternary Centers

ACS catalysis, 2019-04, Vol.9 (4), p.3716-3724

2019

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Synthesis of 2,6-dioxabicyclo[3.3.0]octenes by tandem ring-rearrangement/cross metathesis

Tetrahedron letters, 2008-09, Vol.49 (36), p.5238-5240

2008

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Chemoselective Activation of sp 3 vs sp 2 C–H Bonds with Pd(II)

Journal of the American Chemical Society, 2015-01, Vol.137 (1), p.18-21

2015

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One-pot palladium-catalyzed synthesis of sulfonyl fluorides from aryl bromidesElectronic supplementary information (ESI) available: Experimental details and supporting characterisation data. See DOI: 10.1039/c6sc03924c

2017-01

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One-pot palladium-catalyzed synthesis of sulfonyl fluorides from aryl bromides† †Electronic supplementary information (ESI) available: Experimental details and supporting characterisation data. See DOI: 10.1039/c6sc03924c Click here for additional data file

Chemical science (Cambridge), 2016-10, Vol.8 (2), p.1233-1237

2016

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Facile synthesis of (−)-6-acetoxy-5-hexadecanolide by size-selective ring-closing/cross metathesis

Tetrahedron letters, 2009-12, Vol.50 (51), p.7121-7123

2009

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ChemInform Abstract: Chemoselective Activation of sp3 vs sp2 C-H Bonds with Pd(II)

ChemInform, 2015-07, Vol.46 (27), p.no-no

2015

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Support of academic synthetic chemistry using separation technologies from the pharmaceutical industryElectronic supplementary information (ESI) available. See DOI: 10.1039/c3ob42195c

2014-03

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ChemInform Abstract: One‐Step Synthesis of Sulfonamides from N‐Tosylhydrazones

ChemInform, 2016-06, Vol.47 (25), p.no-no

2016

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Part I: Asymmetric synthesis of α-allyl-α-aryl α-amino acids. Part II: Asymmetric spirocyclization of allenyl ketones. Part III: Chemoselective activation of C(sp3)–H bond over C(sp 2)–H bond with Pd(II)

Curto, John M

2014

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ChemInform Abstract: Chemoselective Activation of sp 3 vs sp 2 C—H Bonds with Pd(II)

ChemInform, 2015-07, Vol.46 (27)

2015

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One-pot palladium-catalyzed synthesis of sulfonyl fluorides from aryl bromides

Mild Aromatic Palladium-Catalyzed Protodecarboxylation: Kinetic Assessment of the Decarboxylative Palladation and the Protodepalladation Steps

Chemoselective activation of sp(3) vs sp(2) C-H bonds with Pd(II)

Palladium-Catalyzed Chemoselective Activation of sp3 vs sp2 C–H Bonds: Oxidative Coupling To Form Quaternary Centers

A General Synthesis of Dihydronaphthyridinones with Aryl-Substituted Quaternary Benzylic Centers

One-Step Synthesis of Sulfonamides from N‑Tosylhydrazones

A Small-Molecule Oral Agonist of the Human Glucagon-like Peptide‑1 Receptor

Preparation of Azinones from (Cyclopropylmethoxy)azine Ethers

Asymmetric Synthesis of α‑Allyl-α-Aryl α‑Amino Acids by Tandem Alkylation/π-Allylation of α‑Iminoesters

Lewis Acid-Promoted Enantioselective Dearomative Spirocyclizations of Allenes

α‑Allyl-α-aryl α‑Amino Esters in the Asymmetric Synthesis of Acyclic and Cyclic Amino Acid Derivatives by Alkene Metathesis

6-Azaspiro[2.5]octanes as small molecule agonists of the human glucagon-like peptide-1 receptor

Chemoselective Activation of sp3 vs sp2 C–H Bonds with Pd(II)

Support of academic synthetic chemistry using separation technologies from the pharmaceutical industry

Palladium-Catalyzed Chemoselective Activation of sp 3 vs sp 2 C-H Bonds: Oxidative Coupling To Form Quaternary Centers

Synthesis of 2,6-dioxabicyclo[3.3.0]octenes by tandem ring-rearrangement/cross metathesis

Chemoselective Activation of sp 3 vs sp 2 C–H Bonds with Pd(II)

One-pot palladium-catalyzed synthesis of sulfonyl fluorides from aryl bromidesElectronic supplementary information (ESI) available: Experimental details and supporting characterisation data. See DOI: 10.1039/c6sc03924c

One-pot palladium-catalyzed synthesis of sulfonyl fluorides from aryl bromides† †Electronic supplementary information (ESI) available: Experimental details and supporting characterisation data. See DOI: 10.1039/c6sc03924c Click here for additional data file

Facile synthesis of (−)-6-acetoxy-5-hexadecanolide by size-selective ring-closing/cross metathesis

ChemInform Abstract: Chemoselective Activation of sp3 vs sp2 C-H Bonds with Pd(II)

Support of academic synthetic chemistry using separation technologies from the pharmaceutical industryElectronic supplementary information (ESI) available. See DOI: 10.1039/c3ob42195c

ChemInform Abstract: One‐Step Synthesis of Sulfonamides from N‐Tosylhydrazones

Part I: Asymmetric synthesis of α-allyl-α-aryl α-amino acids. Part II: Asymmetric spirocyclization of allenyl ketones. Part III: Chemoselective activation of C(sp3)–H bond over C(sp 2)–H bond with Pd(II)

ChemInform Abstract: Chemoselective Activation of sp 3 vs sp 2 C—H Bonds with Pd(II)

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