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Visible-light-mediated oxidative arylation of vinylarenes under aerobic conditions

Catalysis science & technology, 2015-01, Vol.5 (2), p.830-834

2015

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Visible-Light-Induced Meerwein Cascade Reactions for the Preparation of α-Aryl Esters

European journal of organic chemistry, 2015-09, Vol.2015 (26), p.5775-5780

2015

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Chemoselective Preparation of Unsymmetrical Bis(1,2,3-triazole) Derivatives and Application in Bis(1,2,3-triazole)-Modified Peptidomimetic Synthesis

European journal of organic chemistry, 2012-12, Vol.2012 (34), p.6767-6776

2012

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A One-Pot Tandem Ugi Multicomponent Reaction (MCR)/Click Reaction as an Efficient Protecting-Group-Free Route to 1H-1,2,3-Triazole-Modified α-Amino Acid Derivatives and Peptidomimetics

Helvetica chimica acta, 2012-01, Vol.95 (1), p.87-99

2012

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Molecular Iodine Catalyzed Hydroxysulfenylation of Alkenes with Disulfides in Aerobic Conditions

Synlett, 2019-09, Vol.30 (15), p.1830-1834

2019

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Visible-Light-Induced Chemoselective Synthesis of α-Chloro and Vinyl Sulfones by Sulfonylation of Alkenes

Synlett, 2018-02, Vol.29 (3), p.364-368

2018

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Visible-light-promoted oxidative difunctionalization of alkenes with sulfonyl chlorides to access β-keto sulfones under aerobic conditions

Tetrahedron letters, 2017-09, Vol.58 (37), p.3667-3671

2017

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A visible-light-induced chemoselective radical/oxidative addition domino process to access α-chloro and α-alkoxy aryl ketones

Chemical communications (Cambridge, England), 2016-01, Vol.52 (89), p.13105-13108

2016

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Visible light promoted copper-catalyzed Markovnikov hydration of alkynes at room temperature

Tetrahedron letters, 2017-03, Vol.58 (12), p.1156-1159

2017

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Chemoselective preparation of 1,2,3-triazole-isoxazole bisfunctional derivatives and their application in peptidomimetic synthesis

Organic & biomolecular chemistry, 2013-02, Vol.11 (6), p.1040-1048

2013

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Copper-free Route to Triazole-Modified Peptidomimetic by the Combination of Two Multicomponent Reactions in One Pot

ACS combinatorial science, 2012-05, Vol.14 (5), p.309-315

2012

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Synthesis of highly functionalized macrocycles by tandem multicomponent reactions and intramolecular Sonogashira cross-coupling

Organic & biomolecular chemistry, 2013-11, Vol.11 (41), p.7232-7238

2013

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Visible-Light-Induced Meerwein Cascade Reactions for the Preparation of [alpha]-Aryl Esters

European journal of organic chemistry, 2015-09, Vol.2015 (26), p.5775

2015

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A visible-light-induced chemoselective radical/oxidative addition domino process to access α-chloro and α-alkoxy aryl ketonesElectronic supplementary information (ESI) available: Experimental procedures and NMR spectra. See DOI: 10.1039/c6cc07272k

2016-11

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Visible-light-mediated oxidative arylation of vinylarenes under aerobic conditionsElectronic supplementary information (ESI) available. See DOI: 10.1039/c4cy01523a

2015-01

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A One‐Pot Tandem Ugi Multicomponent Reaction (MCR)/Click Reaction as an Efficient Protecting‐Group‐Free Route to 1 H ‐1,2,3‐Triazole‐Modified α ‐Amino Acid Derivatives and Peptidomimetics

Helvetica chimica acta, 2012-01, Vol.95 (1), p.87-99

2012

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Correction to Copper-Free Route to Triazole-Modified Peptidomimetic by the Combination of Two Multicomponent Reactions in One Pot

ACS combinatorial science, 2012-07, Vol.14 (7), p.442-442

2012

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Chemoselective preparation of 1,2,3-triazole-isoxazole bisfunctional derivatives and their application in peptidomimetic synthesisElectronic supplementary information (ESI) available. CCDC 906081. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2ob26990b

2013-01

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ChemInform Abstract: A One-Pot Tandem Ugi Multicomponent Reaction (MCR)/Click Reaction as an Efficient Protecting-Group-Free Route to 1H-1,2,3-Triazole-Modified α-Amino Acid Derivatives and Peptidomimetics

ChemInform, 2012-06, Vol.43 (23), p.no-no

2012

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The Ugi Reaction in a Polyethylene Glycol Medium: A Mild, Protocol for the Production of Compound Libraries

Journal of chemical research, 2011-08, Vol.35 (8), p.444-447

2011

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ChemInform Abstract: Chemoselective Preparation of Unsymmetrical Bis(1,2,3-triazole) Derivatives and Application in Bis(1,2,3-triazole)-Modified Peptidomimetic Synthesis

ChemInform, 2013-05, Vol.44 (19), p.no-no

2013

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ChemInform Abstract: Synthesis of Highly Functionalized Macrocycles by Tandem Multicomponent Reactions and Intramolecular Sonogashira Cross-Coupling

ChemInform, 2014-03, Vol.45 (9), p.no-no

2014

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ChemInform Abstract: The Ugi Reaction in a Polyethylene Glycol Medium: A Mild, Protocol for the Production of Compound Libraries

ChemInform, 2012-01, Vol.43 (1), p.no-no

2012

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The Ugi reaction in a polyethylene glycol medium: a mild, protocol for the production of compound libraries

Journal of chemical research, 2011-08, Vol.35 (8), p.444-447

2011

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One-step generation of p53 gene biallelic mutant Cynomolgus monkey via the CRISPR/Cas system

Cell research, 2015-02, Vol.25 (2), p.258-261

2015

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Visible-light-mediated oxidative arylation of vinylarenes under aerobic conditions

Visible-Light-Induced Meerwein Cascade Reactions for the Preparation of α-Aryl Esters

Chemoselective Preparation of Unsymmetrical Bis(1,2,3-triazole) Derivatives and Application in Bis(1,2,3-triazole)-Modified Peptidomimetic Synthesis

A One-Pot Tandem Ugi Multicomponent Reaction (MCR)/Click Reaction as an Efficient Protecting-Group-Free Route to 1H-1,2,3-Triazole-Modified α-Amino Acid Derivatives and Peptidomimetics

Molecular Iodine Catalyzed Hydroxysulfenylation of Alkenes with Disulfides in Aerobic Conditions

Visible-Light-Induced Chemoselective Synthesis of α-Chloro and Vinyl Sulfones by Sulfonylation of Alkenes

Visible-light-promoted oxidative difunctionalization of alkenes with sulfonyl chlorides to access β-keto sulfones under aerobic conditions

A visible-light-induced chemoselective radical/oxidative addition domino process to access α-chloro and α-alkoxy aryl ketones

Visible light promoted copper-catalyzed Markovnikov hydration of alkynes at room temperature

Chemoselective preparation of 1,2,3-triazole-isoxazole bisfunctional derivatives and their application in peptidomimetic synthesis

Copper-free Route to Triazole-Modified Peptidomimetic by the Combination of Two Multicomponent Reactions in One Pot

Synthesis of highly functionalized macrocycles by tandem multicomponent reactions and intramolecular Sonogashira cross-coupling

Visible-Light-Induced Meerwein Cascade Reactions for the Preparation of [alpha]-Aryl Esters

A visible-light-induced chemoselective radical/oxidative addition domino process to access α-chloro and α-alkoxy aryl ketonesElectronic supplementary information (ESI) available: Experimental procedures and NMR spectra. See DOI: 10.1039/c6cc07272k

Visible-light-mediated oxidative arylation of vinylarenes under aerobic conditionsElectronic supplementary information (ESI) available. See DOI: 10.1039/c4cy01523a

A One‐Pot Tandem Ugi Multicomponent Reaction (MCR)/Click Reaction as an Efficient Protecting‐Group‐Free Route to 1 H ‐1,2,3‐Triazole‐Modified α ‐Amino Acid Derivatives and Peptidomimetics

Correction to Copper-Free Route to Triazole-Modified Peptidomimetic by the Combination of Two Multicomponent Reactions in One Pot

Chemoselective preparation of 1,2,3-triazole-isoxazole bisfunctional derivatives and their application in peptidomimetic synthesisElectronic supplementary information (ESI) available. CCDC 906081. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2ob26990b

ChemInform Abstract: A One-Pot Tandem Ugi Multicomponent Reaction (MCR)/Click Reaction as an Efficient Protecting-Group-Free Route to 1H-1,2,3-Triazole-Modified α-Amino Acid Derivatives and Peptidomimetics

The Ugi Reaction in a Polyethylene Glycol Medium: A Mild, Protocol for the Production of Compound Libraries

ChemInform Abstract: Chemoselective Preparation of Unsymmetrical Bis(1,2,3-triazole) Derivatives and Application in Bis(1,2,3-triazole)-Modified Peptidomimetic Synthesis

ChemInform Abstract: Synthesis of Highly Functionalized Macrocycles by Tandem Multicomponent Reactions and Intramolecular Sonogashira Cross-Coupling

ChemInform Abstract: The Ugi Reaction in a Polyethylene Glycol Medium: A Mild, Protocol for the Production of Compound Libraries

The Ugi reaction in a polyethylene glycol medium: a mild, protocol for the production of compound libraries

One-step generation of p53 gene biallelic mutant Cynomolgus monkey via the CRISPR/Cas system

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