UB Paderborn / Katalog / Suche / in CDI

Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki–Miyaura and Negishi Cross-Coupling Reactions for Tetra-ortho-Substituted Biaryl Synthesis

ACS catalysis, 2018-11, Vol.8 (11), p.10190-10209

2018

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Large-Scale Synthesis of Chiral Tetrahydropyran via Asymmetric Allylation Catalyzed by (S)‑3,3′-Cl2‑BINOL

Organic process research & development, 2022-10, Vol.26 (10), p.2973-2978

2022

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Large-Scale Synthesis of Chiral Tetrahydropyran via Asymmetric Allylation Catalyzed by ( S )-3,3′-Cl 2 -BINOL

Organic process research & development, 2022-10, Vol.26 (10), p.2973-2978

2022

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Practical Synthesis of Terminal Vinyl Fluorides

Journal of organic chemistry, 2023-08, Vol.88 (15), p.10881-10904

2023

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Large Scale Practical Synthesis of Enantiomerically Pure cis-4-Amino-3-fluoro-1-methylpiperidine via Rhodium-Catalyzed Asymmetric Hydrogenation of a Tetrasubstituted Fluoroalkene

Organic process research & development, 2021-03, Vol.25 (3), p.583-590

2021

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Enantioselective Synthesis of α‑(Hetero)aryl Piperidines through Asymmetric Hydrogenation of Pyridinium Salts and Its Mechanistic Insights

Organic letters, 2018-03, Vol.20 (5), p.1333-1337

2018

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Building a Quaternary Stereogenic Center on Dihydroazaindole Carboxylic Acid through Scalable Process Development

Organic process research & development, 2023-11, Vol.27 (11), p.2045-2056

2023

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Sulfone-Mediated SNAr Reaction as a Powerful Tool for the Synthesis of 4‑Quinolinyl Ethers and MoreApplication to the Synthesis of HCV NS3/4a Protease Inhibitor BI 201420

Journal of organic chemistry, 2020-07, Vol.85 (13), p.8339-8351

2020

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Scalable Process of Spiro(cyclopropane)oxazepane Pyridine Carboxylic Acid through Kulinkovich, Mitsunobu, and Pd-Catalyzed Intramolecular C–N Coupling

Organic process research & development, 2022-09, Vol.26 (9), p.2779-2787

2022

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Synthesis of BI 894416 and BI 1342561, two potent and selective spleen tyrosine kinase inhibitors, labeled with carbon 14 and with deuterium

Journal of labelled compounds & radiopharmaceuticals, 2023-04, Vol.66 (4-6), p.155-168

2023

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Structure Elucidation of a Complex Faldaprevir-(±)-[alpha]-Tocopherol Addition Product Reveals Reactivity of Common Excipient Vitamin E-TPGS

Journal of heterocyclic chemistry, 2016-11, Vol.53 (6), p.1878

2016

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Structure Elucidation of a Complex Faldaprevir-(±)-α-Tocopherol Addition Product Reveals Reactivity of Common Excipient Vitamin E-TPGS

Journal of heterocyclic chemistry, 2016-11, Vol.53 (6), p.1878-1891

2016

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A Mild Dihydrobenzooxaphosphole Oxazoline/Iridium Catalytic System for Asymmetric Hydrogenation of Unfunctionalized Dialins

Angewandte Chemie (International ed.), 2014-12, Vol.53 (52), p.14428-14432

International ed. in English, 2014

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Synthesis of stable isotope‐labelled firocoxib

Journal of labelled compounds & radiopharmaceuticals, 2020-06, Vol.63 (8), p.386-392

2020

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Sulfone-Mediated S N Ar Reaction as a Powerful Tool for the Synthesis of 4-Quinolinyl Ethers and More-Application to the Synthesis of HCV NS3/4a Protease Inhibitor BI 201420

Journal of organic chemistry, 2020-07, Vol.85 (13), p.8339-8351

2020

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Development of a Scalable, Chromatography-Free Synthesis of t -Bu-SMS-Phos and Application to the Synthesis of an Important Chiral CF 3 -Alcohol Derivative with High Enantioselectivity Using Rh-Catalyzed Asymmetric Hydrogenation

Journal of organic chemistry, 2018-02, Vol.83 (3), p.1448-1461

2018

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Automated Solid Phase Extraction (SPE) LC/NMR Applied to the Structural Analysis of Extractable Compounds from a Pharmaceutical Packaging Material of Construction

PDA journal of pharmaceutical science and technology, 2013-05, Vol.67 (3), p.267

2013

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HPLC and LC/MS Analysis of Pharmaceutical Container Closure System Leachables and Extractables

Journal of liquid chromatography & related technologies, 2009-06, Vol.32 (11-12), p.1768-1827

2009

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Identification of a process impurity formed during synthesis of a nevirapine analogue HIV NNRT inhibitor using LC/MS and forced degradation studies

Journal of pharmaceutical and biomedical analysis, 2009-04, Vol.49 (3), p.733-738

2009

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A Mild Dihydrobenzooxaphosphole Oxazoline/Iridium Catalytic System for Asymmetric Hydrogenation of Unfunctionalized Dialins

Angewandte Chemie, 2014-12, Vol.126 (52), p.14656-14660

2014

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Identification of Drug Meglumine Interaction Products Using LC/MS and Forced Degradation Studies

Journal of liquid chromatography & related technologies, 2008-08, Vol.31 (15), p.2331-2336

2008

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Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki–Miyaura and Negishi Cross-Coupling Reactions for Tetra-ortho-Substituted Biaryl Synthesis

Large-Scale Synthesis of Chiral Tetrahydropyran via Asymmetric Allylation Catalyzed by (S)‑3,3′-Cl2‑BINOL

Large-Scale Synthesis of Chiral Tetrahydropyran via Asymmetric Allylation Catalyzed by ( S )-3,3′-Cl 2 -BINOL

Practical Synthesis of Terminal Vinyl Fluorides

Large Scale Practical Synthesis of Enantiomerically Pure cis-4-Amino-3-fluoro-1-methylpiperidine via Rhodium-Catalyzed Asymmetric Hydrogenation of a Tetrasubstituted Fluoroalkene

Enantioselective Synthesis of α‑(Hetero)aryl Piperidines through Asymmetric Hydrogenation of Pyridinium Salts and Its Mechanistic Insights

Building a Quaternary Stereogenic Center on Dihydroazaindole Carboxylic Acid through Scalable Process Development

Sulfone-Mediated SNAr Reaction as a Powerful Tool for the Synthesis of 4‑Quinolinyl Ethers and MoreApplication to the Synthesis of HCV NS3/4a Protease Inhibitor BI 201420

Scalable Process of Spiro(cyclopropane)oxazepane Pyridine Carboxylic Acid through Kulinkovich, Mitsunobu, and Pd-Catalyzed Intramolecular C–N Coupling

Synthesis of BI 894416 and BI 1342561, two potent and selective spleen tyrosine kinase inhibitors, labeled with carbon 14 and with deuterium

Structure Elucidation of a Complex Faldaprevir-(±)-[alpha]-Tocopherol Addition Product Reveals Reactivity of Common Excipient Vitamin E-TPGS

Structure Elucidation of a Complex Faldaprevir-(±)-α-Tocopherol Addition Product Reveals Reactivity of Common Excipient Vitamin E-TPGS

A Mild Dihydrobenzooxaphosphole Oxazoline/Iridium Catalytic System for Asymmetric Hydrogenation of Unfunctionalized Dialins

Process Development of the BACE Inhibitors BI 1147560 BS and BI 1181181 MZ

Synthesis of stable isotope‐labelled firocoxib

Sulfone-Mediated S N Ar Reaction as a Powerful Tool for the Synthesis of 4-Quinolinyl Ethers and More-Application to the Synthesis of HCV NS3/4a Protease Inhibitor BI 201420

Development of a Scalable, Chromatography-Free Synthesis of t‑Bu-SMS-Phos and Application to the Synthesis of an Important Chiral CF3‑Alcohol Derivative with High Enantioselectivity Using Rh-Catalyzed Asymmetric Hydrogenation

Development of a Scalable, Chromatography-Free Synthesis of t -Bu-SMS-Phos and Application to the Synthesis of an Important Chiral CF 3 -Alcohol Derivative with High Enantioselectivity Using Rh-Catalyzed Asymmetric Hydrogenation

Correction to “Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki–Miyaura and Negishi Cross-Coupling Reactions for Tetra-ortho-Substituted Biaryl Synthesis”

Automated Solid Phase Extraction (SPE) LC/NMR Applied to the Structural Analysis of Extractable Compounds from a Pharmaceutical Packaging Material of Construction

HPLC and LC/MS Analysis of Pharmaceutical Container Closure System Leachables and Extractables

Identification of a process impurity formed during synthesis of a nevirapine analogue HIV NNRT inhibitor using LC/MS and forced degradation studies

Development of a Scalable, Chromatography-Free Synthesis of t-Bu-SMS-Phos and Application to the Synthesis of an Important Chiral CF3-Alcohol Derivative in High Enantioselectivity Using Rh-Catalyzed Asymmetric Hydrogenation

A Mild Dihydrobenzooxaphosphole Oxazoline/Iridium Catalytic System for Asymmetric Hydrogenation of Unfunctionalized Dialins

Identification of Drug Meglumine Interaction Products Using LC/MS and Forced Degradation Studies

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