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Describing oxymethylene ether synthesis based on the application of non-stoichiomsetric Gibbs minimisation

Reaction chemistry & engineering, 2018-06, Vol.3 (3), p.277-292

2018

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Prozesssimulation des komplexen Gemischverhaltens von Oxymethylendimethylether (OME)

Chemie ingenieur technik, 2020-09, Vol.92 (9), p.1301-1301

2020

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Technoökonomische und ökologische Bewertung synthetischer flüssiger Energieträger – Power‐to‐Methanol und ‐OME

Chemie ingenieur technik, 2018-09, Vol.90 (9), p.1138-1138

2018

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Describing oxymethylene ether synthesis based on the application of non-stoichiomsetric Gibbs minimisationElectronic supplementary information (ESI) available: Algorithm for Gibbs energy minimisation technique, Algorithm for recycle calculation, tables for standard thermodynamic properties, tables for UNIFAC parameters, experimental setup schematic, model validation against experimental and literature simulation data. See DOI: 10.1039/c8re00006a

2018-06

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Facile Two‐Phase Catalysis: From Dimethoxymethane and Monomeric Formaldehyde towards Oxymethylene Ethers (OMEs)

ChemCatChem, 2020-05, Vol.12 (9), p.2416-2420

2020

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Jagged1-dependent Notch signaling is dispensable for hematopoietic stem cell self-renewal and differentiation

Blood, 2005-03, Vol.105 (6), p.2340-2342

2005

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Enabling, Decagram-Scale Synthesis of Macrocyclic MCL‑1 Inhibitor ABBV-467

Journal of organic chemistry, 2023-11, Vol.88 (22), p.15562-15568

2023

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Jagged1 signals in the postnatal subventricular zone are required for neural stem cell self-renewal

The EMBO journal, 2005-10, Vol.24 (19), p.3504-3515

2005

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Quantifying the Early Stages of Remyelination Following Cuprizone-induced Demyelination

Brain pathology (Zurich, Switzerland), 2003-07, Vol.13 (3), p.329-339

2003

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Methylpyrrole inhibitors of BET bromodomains

Bioorganic & medicinal chemistry letters, 2017-05, Vol.27 (10), p.2225-2233

2017

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Discovery and optimization of novel constrained pyrrolopyridone BET family inhibitors

Bioorganic & medicinal chemistry letters, 2018-06, Vol.28 (10), p.1804-1810

2018

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The Raft-Associated Protein MAL Is Required for Maintenance of Proper Axon-Glia Interactions in the Central Nervous System

The Journal of cell biology, 2004-08, Vol.166 (5), p.731-742

2004

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Notch1 Control of Oligodendrocyte Differentiation in the Spinal Cord

The Journal of cell biology, 2002-08, Vol.158 (4), p.709-718

2002

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Notch1 and Jagged1 are expressed after CNS demyelination, but are not a major rate-determining factor during remyelination

Brain (London, England : 1878), 2004-09, Vol.127 (9), p.1928-1941

2004

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An initiator and its flanking elements function as a core promoter driving transcription of the Hepatopoietin gene

FEBS letters, 2003-04, Vol.540 (1), p.58-64

2003

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Substituted 4-amino-1H-pyrazolo[3,4-d]pyrimidines as multi-targeted inhibitors of insulin-like growth factor-1 receptor (IGF1R) and members of ErbB-family receptor kinases

Bioorganic & medicinal chemistry letters, 2010-10, Vol.20 (20), p.6067-6071

2010

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Industrial-Scale Fabrication of Optical Components Using High-Precision 3D Printing: Aspects-Applications-Perspectives

3D Printing of Optical Components, 2021, Vol.233, p.185-237

2021

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Imidazo[2,1- b]thiazoles: Multitargeted inhibitors of both the insulin-like growth factor receptor and members of the epidermal growth factor family of receptor tyrosine kinases

Bioorganic & medicinal chemistry letters, 2010-04, Vol.20 (8), p.2452-2455

2010

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Pyridone-Containing farnesyltransferase inhibitors: synthesis and biological evaluation

Bioorganic & medicinal chemistry letters, 2003-11, Vol.13 (22), p.4001-4005

2003

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Methylpyrrole inhibitors of BET bromodomains

Bioorganic & medicinal chemistry letters, 2017-05, Vol.27 (10)

2017

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Handbook of Research on Teaching the English Language Arts

Fourth edition, 2018

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Naphthamidine urokinase plasminogen activator inhibitors with improved pharmacokinetic properties

Bioorganic & medicinal chemistry letters, 2005-01, Vol.15 (1), p.93-98

2005

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Abstract A248: Substituted 4-amino-1 H -pyrazolo[3,4- d ]pyrimidines as multitargeted inhibitors targeting insulin-like growth factor-1 receptor (IGF1R) and members of ErbB-family receptor tyrosine kinases

Molecular cancer therapeutics, 2009-12, Vol.8 (12_Supplement), p.A248-A248

2009

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Describing oxymethylene ether synthesis based on the application of non-stoichiomsetric Gibbs minimisation

Prozesssimulation des komplexen Gemischverhaltens von Oxymethylendimethylether (OME)

Technoökonomische und ökologische Bewertung synthetischer flüssiger Energieträger – Power‐to‐Methanol und ‐OME

Discovery of N‑(4-(2,4-Difluorophenoxy)-3-(6-methyl-7-oxo-6,7-dihydro‑1H‑pyrrolo[2,3‑c]pyridin-4-yl)phenyl)ethanesulfonamide (ABBV-075/Mivebresib), a Potent and Orally Available Bromodomain and Extraterminal Domain (BET) Family Bromodomain Inhibitor

Facile Two‐Phase Catalysis: From Dimethoxymethane and Monomeric Formaldehyde towards Oxymethylene Ethers (OMEs)

Jagged1-dependent Notch signaling is dispensable for hematopoietic stem cell self-renewal and differentiation

Enabling, Decagram-Scale Synthesis of Macrocyclic MCL‑1 Inhibitor ABBV-467

Fragment-Based, Structure-Enabled Discovery of Novel Pyridones and Pyridone Macrocycles as Potent Bromodomain and Extra-Terminal Domain (BET) Family Bromodomain Inhibitors

Jagged1 signals in the postnatal subventricular zone are required for neural stem cell self-renewal

Quantifying the Early Stages of Remyelination Following Cuprizone-induced Demyelination

Methylpyrrole inhibitors of BET bromodomains

Discovery and optimization of novel constrained pyrrolopyridone BET family inhibitors

The Raft-Associated Protein MAL Is Required for Maintenance of Proper Axon-Glia Interactions in the Central Nervous System

Notch1 Control of Oligodendrocyte Differentiation in the Spinal Cord

Notch1 and Jagged1 are expressed after CNS demyelination, but are not a major rate-determining factor during remyelination

An initiator and its flanking elements function as a core promoter driving transcription of the Hepatopoietin gene

Substituted 4-amino-1H-pyrazolo[3,4-d]pyrimidines as multi-targeted inhibitors of insulin-like growth factor-1 receptor (IGF1R) and members of ErbB-family receptor kinases

Industrial-Scale Fabrication of Optical Components Using High-Precision 3D Printing: Aspects-Applications-Perspectives

Imidazo[2,1- b]thiazoles: Multitargeted inhibitors of both the insulin-like growth factor receptor and members of the epidermal growth factor family of receptor tyrosine kinases

Pyridone-Containing farnesyltransferase inhibitors: synthesis and biological evaluation

Methylpyrrole inhibitors of BET bromodomains

Handbook of Research on Teaching the English Language Arts

Naphthamidine urokinase plasminogen activator inhibitors with improved pharmacokinetic properties

Abstract A248: Substituted 4-amino-1 H -pyrazolo[3,4- d ]pyrimidines as multitargeted inhibitors targeting insulin-like growth factor-1 receptor (IGF1R) and members of ErbB-family receptor tyrosine kinases

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