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Homogeneous catalysis for the production of low-volume, high-value chemicals from biomass

Nature reviews. Chemistry, 2018-05, Vol.2 (5), p.35-46

2018

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Diastereoselective B(C6F5)3‑Catalyzed Reductive Carbocyclization of Unsaturated Carbohydrates

Organic letters, 2016-08, Vol.18 (16), p.4120-4123

2016

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Enantioselective Synthesis of Quaternary Carbon Stereogenic Centers through Copper-Catalyzed Conjugate Additions of Aryl- and Alkylaluminum Reagents to Acyclic Trisubstituted Enones

Angewandte Chemie (International ed.), 2013-07, Vol.52 (31), p.8156-8159

International ed. in English, 2013

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Delineating The Multiple Roles of B(C6F5)3 in the Chemoselective Deoxygenation of Unsaturated Polyols

ACS catalysis, 2016-12, Vol.6 (12), p.8399-8403

2016

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Enantioselective Synthesis of Alkyne-Substituted Quaternary Carbon Stereogenic Centers through NHC−Cu-Catalyzed Allylic Substitution Reactions with (i-Bu)2(Alkynyl)aluminum Reagents

Journal of the American Chemical Society, 2011-04, Vol.133 (13), p.4778-4781

2011

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Combining NHC-Cu and Brønsted Base Catalysis: Enantioselective Allylic Substitution/Conjugate Additions with Alkynylaluminum Reagents and Stereospecific Isomerization of the Products to Trisubstituted Allenes

Angewandte Chemie (International ed.), 2013-07, Vol.52 (30), p.7694-7699

International ed. in English, 2013

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Formation of Vinyl-, Vinylhalide- or Acyl-Substituted Quaternary Carbon Stereogenic Centers through NHC−Cu-Catalyzed Enantioselective Conjugate Additions of Si-Containing Vinylaluminums to β-Substituted Cyclic Enones

Journal of the American Chemical Society, 2011-02, Vol.133 (4), p.736-739

2011

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Chemoselective conversion of biologically sourced polyols into chiral synthons

Nature chemistry, 2015-07, Vol.7 (7), p.576-581

2015

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Design of Culinary Transformations: A Chemistry Course for Nonscience Majors

Journal of chemical education, 2020-05, Vol.97 (5), p.1283-1288

2020

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Recipe Modification as a Means of Learning and Applying the Scientific Method

Journal of chemical education, 2021-05, Vol.98 (5), p.1610-1621

2021

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Enantioselective Synthesis of Quaternary Carbon Stereogenic Centers through Copper-Catalyzed Conjugate Additions of Aryl- and Alkylaluminum Reagents to Acyclic Trisubstituted Enones

Angewandte Chemie, 2013-07, Vol.125 (31), p.8314-8317

2013

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Catalytic and Regioselective Ring Expansion of Arylcyclobutanones with Trimethylsilyldiazomethane. Ligand-Dependent Entry to β-Ketosilane or Enolsilane Adducts

Organic letters, 2010-08, Vol.12 (16), p.3598-3601

2010

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Correction to “Formation of Vinyl‑, Vinylhalide- or Acyl-Substituted Quaternary Carbon Stereogenic Centers through NHC–Cu-Catalyzed Enantioselective Conjugate Additions of Si-Containing Vinylaluminums to β‑Substituted Cyclic Enones”

Journal of the American Chemical Society, 2014-07, Vol.136 (29), p.10544-10544

2014

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Erratum: Chemoselective conversion of biologically sourced polyols into chiral synthons

Nature chemistry, 2015-09, Vol.7 (9), p.759-759

2015

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Combining NHC-Cu and Brønsted Base Catalysis: Enantioselective Allylic Substitution/Conjugate Additions with Alkynylaluminum Reagents and Stereospecific Isomerization of the Products to Trisubstituted Allenes

Angewandte Chemie, 2013-07, Vol.125 (30), p.7848-7853

2013

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Combining NHC-Cu and Broensted Base Catalysis: Enantioselective Allylic Substitution/Conjugate Additions with Alkynylaluminum Reagents and Stereospecific Isomerization of the Products to Trisubstituted Allenes

Angewandte Chemie International Edition, 2013-07, Vol.52 (30), p.7694-7699

2013

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Combining NHC-Cu and Brønsted Base Catalysis: Enantioselective Allylic Substitution/Conjugate Addition with Alkynylaluminum Reagents and their Stereospecific Isomerization to Trisubstituted Allenes

Angewandte Chemie (International ed.), 2013-06, Vol.52 (30), p.7694-7699

2013

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Enantioselective Synthesis of Quaternary Carbon Stereogenic Centers through Cu-Catalyzed Conjugate Additions of Aryl- and Alkylaluminum Reagents to Acyclic Trisubstituted Enones

Angewandte Chemie (International ed.), 2013-06, Vol.52 (31), p.8156-8159

2013

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ChemInform Abstract: Diastereoselective B(C6F5)3‐Catalyzed Reductive Carbocyclization of Unsaturated Carbohydrates

ChemInform, 2016-12, Vol.47 (52), p.no-no

2016

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ChemInform Abstract: Combining NHC-Cu and Broensted Base Catalysis: Enantioselective Allylic Substitution/Conjugate Additions with Alkynylaluminum Reagents and Stereospecific Isomerization of the Products to Trisubstituted Allenes

ChemInform, 2013-12, Vol.44 (49), p.no-no

2013

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ChemInform Abstract: Enantioselective Synthesis of Quaternary Carbon Stereogenic Centers Through Copper-Catalyzed Conjugate Additions of Aryl- and Alkylaluminum Reagents to Acyclic Trisubstituted Enones

ChemInform, 2013-12, Vol.44 (51), p.no-no

2013

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ChemInform Abstract: Enantioselective Synthesis of Alkyne-Substituted Quaternary Carbon Stereogenic Centers Through NHC-Cu-Catalyzed Allylic Substitution Reactions with (iBu)2(Alkynyl)aluminum Reagents

ChemInform, 2011-08, Vol.42 (34), p.no-no

2011

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ChemInform Abstract: Formation of Vinyl-, Vinylhalide- or Acyl-Substituted Quaternary Carbon Stereogenic Centers Through NHC-Cu-Catalyzed Enantioselective Conjugate Additions of Si-Containing Vinylaluminums to β-Substituted Cyclic Enones

ChemInform, 2011-06, Vol.42 (24), p.no-no

2011

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ChemInform Abstract: Catalytic and Regioselective Ring Expansion of Arylcyclobutanones with Trimethylsilyldiazomethane. Ligand-Dependent Entry to β-Ketosilane or Enolsilane Adducts

ChemInform, 2010-12, Vol.41 (51), p.no-no

2010

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Homogeneous catalysis for the production of low-volume, high-value chemicals from biomass

Diastereoselective B(C6F5)3‑Catalyzed Reductive Carbocyclization of Unsaturated Carbohydrates

Enantioselective Synthesis of Quaternary Carbon Stereogenic Centers through Copper-Catalyzed Conjugate Additions of Aryl- and Alkylaluminum Reagents to Acyclic Trisubstituted Enones

Delineating The Multiple Roles of B(C6F5)3 in the Chemoselective Deoxygenation of Unsaturated Polyols

Enantioselective Synthesis of Alkyne-Substituted Quaternary Carbon Stereogenic Centers through NHC−Cu-Catalyzed Allylic Substitution Reactions with (i-Bu)2(Alkynyl)aluminum Reagents

Combining NHC-Cu and Brønsted Base Catalysis: Enantioselective Allylic Substitution/Conjugate Additions with Alkynylaluminum Reagents and Stereospecific Isomerization of the Products to Trisubstituted Allenes

Formation of Vinyl-, Vinylhalide- or Acyl-Substituted Quaternary Carbon Stereogenic Centers through NHC−Cu-Catalyzed Enantioselective Conjugate Additions of Si-Containing Vinylaluminums to β-Substituted Cyclic Enones

Chemoselective conversion of biologically sourced polyols into chiral synthons

Design of Culinary Transformations: A Chemistry Course for Nonscience Majors

Recipe Modification as a Means of Learning and Applying the Scientific Method

Enantioselective Synthesis of Quaternary Carbon Stereogenic Centers through Copper-Catalyzed Conjugate Additions of Aryl- and Alkylaluminum Reagents to Acyclic Trisubstituted Enones

Catalytic and Regioselective Ring Expansion of Arylcyclobutanones with Trimethylsilyldiazomethane. Ligand-Dependent Entry to β-Ketosilane or Enolsilane Adducts

Correction to “Formation of Vinyl‑, Vinylhalide- or Acyl-Substituted Quaternary Carbon Stereogenic Centers through NHC–Cu-Catalyzed Enantioselective Conjugate Additions of Si-Containing Vinylaluminums to β‑Substituted Cyclic Enones”

Erratum: Chemoselective conversion of biologically sourced polyols into chiral synthons

Combining NHC-Cu and Brønsted Base Catalysis: Enantioselective Allylic Substitution/Conjugate Additions with Alkynylaluminum Reagents and Stereospecific Isomerization of the Products to Trisubstituted Allenes

Combining NHC-Cu and Broensted Base Catalysis: Enantioselective Allylic Substitution/Conjugate Additions with Alkynylaluminum Reagents and Stereospecific Isomerization of the Products to Trisubstituted Allenes

Combining NHC-Cu and Brønsted Base Catalysis: Enantioselective Allylic Substitution/Conjugate Addition with Alkynylaluminum Reagents and their Stereospecific Isomerization to Trisubstituted Allenes

Enantioselective Synthesis of Quaternary Carbon Stereogenic Centers through Cu-Catalyzed Conjugate Additions of Aryl- and Alkylaluminum Reagents to Acyclic Trisubstituted Enones

ChemInform Abstract: Diastereoselective B(C6F5)3‐Catalyzed Reductive Carbocyclization of Unsaturated Carbohydrates

ChemInform Abstract: Combining NHC-Cu and Broensted Base Catalysis: Enantioselective Allylic Substitution/Conjugate Additions with Alkynylaluminum Reagents and Stereospecific Isomerization of the Products to Trisubstituted Allenes

ChemInform Abstract: Enantioselective Synthesis of Quaternary Carbon Stereogenic Centers Through Copper-Catalyzed Conjugate Additions of Aryl- and Alkylaluminum Reagents to Acyclic Trisubstituted Enones

ChemInform Abstract: Enantioselective Synthesis of Alkyne-Substituted Quaternary Carbon Stereogenic Centers Through NHC-Cu-Catalyzed Allylic Substitution Reactions with (iBu)2(Alkynyl)aluminum Reagents

ChemInform Abstract: Formation of Vinyl-, Vinylhalide- or Acyl-Substituted Quaternary Carbon Stereogenic Centers Through NHC-Cu-Catalyzed Enantioselective Conjugate Additions of Si-Containing Vinylaluminums to β-Substituted Cyclic Enones

ChemInform Abstract: Catalytic and Regioselective Ring Expansion of Arylcyclobutanones with Trimethylsilyldiazomethane. Ligand-Dependent Entry to β-Ketosilane or Enolsilane Adducts

Comprehensive molecular, genomic and phenotypic analysis of a major clone of Enterococcus faecalis MLST ST40

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