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Microwave-assisted synthesis of indole- and azaindole-derivatives in water via cycloisomerization of 2-alkynylanilines and alkynylpyridinamines promoted by amines or catalytic amounts of neutral or basic salts

Tetrahedron, 2010-08, Vol.66 (35), p.7169-7178

2010

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Convenient copper- and solvent-free Sonogashira-type alkynylation of aryl iodides and bromides using Pd EnCat

Tetrahedron letters, 2009-01, Vol.50 (2), p.204-207

2009

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Microwave-assisted synthesis of indole-derivatives via cycloisomerization of 2-alkynylanilines in water without added catalysts, acids, or bases

Tetrahedron letters, 2009-12, Vol.50 (49), p.6877-6881

2009

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An Optimized Scalable Fully Automated Solid-Phase Microwave-Assisted cGMP-Ready Process for the Preparation of Eptifibatide

Organic process research & development, 2021-03, Vol.25 (3), p.552-563

2021

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An Optimized Safe Process from Bench to Pilot cGMP Production of API Eptifibatide Using a Multigram-Scale Microwave-Assisted Solid-Phase Peptide Synthesizer

Organic process research & development, 2021-12, Vol.25 (12), p.2754-2771

2021

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Corrections to “An Optimized Safe Process from Bench to Pilot cGMP Production of API Eptifibatide Using a Multigram-Scale Microwave-Assisted Solid-Phase Peptide Synthesizer”

Organic process research & development, 2022-08, Vol.26 (8), p.2540-2540

2022

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Mild and convenient one-pot synthesis of 1,3,4-oxadiazoles

Tetrahedron letters, 2010-09, Vol.51 (37), p.4801-4805

2010

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Mild, convenient and versatile Cu-mediated synthesis of N-aryl-2-imidazolidinones

Tetrahedron letters, 2010-06, Vol.51 (24), p.3232-3235

2010

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Identification of a Manufacturing Route of Novel CRF-1 Antagonists Containing a 2,3-Dihydro-1 H -pyrrolo[2,3- b ]pyridine Moiety

Organic process research & development, 2010-07, Vol.14 (4), p.895-901

2010

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Identification of a Manufacturing Route of Novel CRF-1 Antagonists Containing a 2,3-Dihydro-1H-pyrrolo[2,3-b]pyridine Moiety

Organic process research & development, 2010-07, Vol.14 (4), p.895-901

2010

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A multi-technique approach using LC–NMR, LC–MS, semi-preparative HPLC, HR–NMR and HR–MS for the isolation and characterization of low-level unknown impurities in GW876008, a novel corticotropin-release factor 1 antagonist

Journal of pharmaceutical and biomedical analysis, 2010-11, Vol.53 (3), p.517-525

2010

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Overall Synthesis of GSK356278: Quick Delivery of a PDE4 Inhibitor Using a Fit-for-Purpose Approach

Organic process research & development, 2010-09, Vol.14 (5), p.1153-1161

2010

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Fit for Purpose Experimental Designs and Analyses in Chemical Development

Organic process research & development, 2010-03, Vol.14 (2), p.332-338

2010

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Synthesis of the racemic forms of carbon–carbon double bond locked analogues of strobilurins which are characterized by a 2-arylcyclopropane ring cis-substituted at C-1 by the methyl ( E)-3-methoxypropenoate unit

Tetrahedron, 2002-05, Vol.58 (19), p.3673-3680

2002

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An Efficient Scalable Route for the Synthesis of Enantiomerically Pure tert-Butyl-(1R,4S,6R)-4-(hydroxymethyl)-3-azabicyclo[4.1.0]heptane-3-carboxylate

Organic process research & development, 2010-09, Vol.14 (5), p.1239-1247

2010

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Stereocontrolled synthesis of carbon–carbon double bond locked analogues of strobilurins which are characterized by a trans-1,2-disubstituted cyclopropane ring

Tetrahedron, 2001-04, Vol.57 (14), p.2847-2856

2001

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Copper-Catalyzed C–N Coupling on Large Scale: An Industrial Case Study

Transition Metal-Catalyzed Couplings in Process Chemistry, 2013, p.135-145

2013

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ChemInform Abstract: Microwave-Assisted Synthesis of Indole-Derivatives via Cycloisomerization of 2-Alkynylanilines in Water Without Added Catalysts, Acids, or Bases

ChemInform, 2010-03, Vol.41 (12), p.no-no

2010

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ChemInform Abstract: Convenient Copper- and Solvent-Free Sonogashira-Type Alkynylation of Aryl Iodides and Bromides Using Pd EnCat

ChemInform, 2009-04, Vol.40 (15), p.no-no

2009

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ChemInform Abstract: Microwave-Assisted Synthesis of Indole- and Azaindole-Derivatives in Water via Cycloisomerization of 2-Alkynylanilines and Alkynylpyridinamines Promoted by Amines or Catalytic Amounts of Neutral or Basic Salts

ChemInform, 2011-01, Vol.42 (1), p.no-no

2011

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ChemInform Abstract: Mild and Convenient One-Pot Synthesis of 1,3,4-Oxadiazoles

ChemInform, 2010-12, Vol.41 (52), p.no-no

2010

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ChemInform Abstract: Mild, Convenient and Versatile Cu-Mediated Synthesis of N-Aryl-2-imidazolidinones

ChemInform, 2010-10, Vol.41 (40), p.no-no

2010

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ChemInform Abstract: Stereocontrolled Synthesis of Carbon-Carbon Double Bond Locked Analogues of Strobilurins Which Are Characterized by a trans-1,2-Disubstituted Cyclopropane Ring

ChemInform, 2001-07, Vol.32 (31), p.no-no

2001

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Microwave-assisted synthesis of indole- and azaindole-derivatives in water via cycloisomerization of 2-alkynylanilines and alkynylpyridinamines promoted by amines or catalytic amounts of neutral or basic salts

Convenient copper- and solvent-free Sonogashira-type alkynylation of aryl iodides and bromides using Pd EnCat

Microwave-assisted synthesis of indole-derivatives via cycloisomerization of 2-alkynylanilines in water without added catalysts, acids, or bases

An Optimized Scalable Fully Automated Solid-Phase Microwave-Assisted cGMP-Ready Process for the Preparation of Eptifibatide

An Optimized Safe Process from Bench to Pilot cGMP Production of API Eptifibatide Using a Multigram-Scale Microwave-Assisted Solid-Phase Peptide Synthesizer

Corrections to “An Optimized Safe Process from Bench to Pilot cGMP Production of API Eptifibatide Using a Multigram-Scale Microwave-Assisted Solid-Phase Peptide Synthesizer”

Mild and convenient one-pot synthesis of 1,3,4-oxadiazoles

Mild, convenient and versatile Cu-mediated synthesis of N-aryl-2-imidazolidinones

Identification of a Manufacturing Route of Novel CRF-1 Antagonists Containing a 2,3-Dihydro-1 H -pyrrolo[2,3- b ]pyridine Moiety

Identification of a Manufacturing Route of Novel CRF-1 Antagonists Containing a 2,3-Dihydro-1H-pyrrolo[2,3-b]pyridine Moiety

A multi-technique approach using LC–NMR, LC–MS, semi-preparative HPLC, HR–NMR and HR–MS for the isolation and characterization of low-level unknown impurities in GW876008, a novel corticotropin-release factor 1 antagonist

Overall Synthesis of GSK356278: Quick Delivery of a PDE4 Inhibitor Using a Fit-for-Purpose Approach

Fit for Purpose Experimental Designs and Analyses in Chemical Development

Synthesis of the racemic forms of carbon–carbon double bond locked analogues of strobilurins which are characterized by a 2-arylcyclopropane ring cis-substituted at C-1 by the methyl ( E)-3-methoxypropenoate unit

An Efficient Scalable Route for the Synthesis of Enantiomerically Pure tert-Butyl-(1R,4S,6R)-4-(hydroxymethyl)-3-azabicyclo[4.1.0]heptane-3-carboxylate

Stereocontrolled synthesis of carbon–carbon double bond locked analogues of strobilurins which are characterized by a trans-1,2-disubstituted cyclopropane ring

Copper-Catalyzed C–N Coupling on Large Scale: An Industrial Case Study

ChemInform Abstract: Microwave-Assisted Synthesis of Indole-Derivatives via Cycloisomerization of 2-Alkynylanilines in Water Without Added Catalysts, Acids, or Bases

ChemInform Abstract: Convenient Copper- and Solvent-Free Sonogashira-Type Alkynylation of Aryl Iodides and Bromides Using Pd EnCat

ChemInform Abstract: Microwave-Assisted Synthesis of Indole- and Azaindole-Derivatives in Water via Cycloisomerization of 2-Alkynylanilines and Alkynylpyridinamines Promoted by Amines or Catalytic Amounts of Neutral or Basic Salts

ChemInform Abstract: Mild and Convenient One-Pot Synthesis of 1,3,4-Oxadiazoles

ChemInform Abstract: Mild, Convenient and Versatile Cu-Mediated Synthesis of N-Aryl-2-imidazolidinones

ChemInform Abstract: Stereocontrolled Synthesis of Carbon-Carbon Double Bond Locked Analogues of Strobilurins Which Are Characterized by a trans-1,2-Disubstituted Cyclopropane Ring

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