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Characterization of covalent inhibitors that disrupt the interaction between the tandem SH2 domains of SYK and FCER1G phospho-ITAM

PloS one, 2024-02, Vol.19 (2), p.e0293548-e0293548

2024

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Advancements in high-resolution 3D microscopy analysis of endosomal morphology in postmortem Alzheimer's disease brains

Frontiers in neuroscience, 2024-01, Vol.17, p.1321680-1321680

2024

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Pharmacologic enhancement of retromer rescues endosomal pathology induced by defects in the Alzheimer’s gene SORL1

Stem cell reports, 2023-12, Vol.18 (12), p.2434-2450

2023

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The role of glucose in supporting motility and capacitation in human spermatozoa

Journal of andrology, 2001-07, Vol.22 (4), p.680-695

2001

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Altmetrics, huh?

Human reproduction (Oxford), 2016-01, Vol.31 (1), p.1-1

2016

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The war on error

Human reproduction (Oxford), 2015-08, Vol.30 (8), p.1747-1748

2015

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Sazetidine-A is a potent and selective agonist at native and recombinant alpha 4 beta 2 nicotinic acetylcholine receptors

Molecular pharmacology, 2008-06, Vol.73 (6), p.1838-1843

2008

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An alternative strategy to the Pictet–Spengler method for tetrahydroisoquinoline synthesis: a feasibility study

Tetrahedron letters, 2012-08, Vol.53 (35), p.4657-4660

2012

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Optimised conditions for styrene syntheses using Suzuki–Miyaura couplings and catalyst-ligand-base pre-mixes

Tetrahedron letters, 2012-08, Vol.53 (35), p.4654-4656

2012

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Selenocyclisations of homoallylic sulfonamides: stereoselective methods for the elaboration of substituted pyrrolidines, pyrrolines and derivatives

Tetrahedron, 2006-09, Vol.62 (39), p.9247-9257

2006

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Acylnitrilium ion-initiated heteroannulations in alkaloid synthesis. An efficient, stereocontrolled, total synthesis of the Orchidaceae alkaloid (.+-.)-dendrobine

Journal of the American Chemical Society, 1992-05, Vol.114 (11), p.4089-4095

1992

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Sazetidine-A Is a Potent and Selective Agonist at Native and Recombinant α4β2 Nicotinic Acetylcholine Receptors

Molecular pharmacology, 2008-06, Vol.73 (6), p.1838-1843

2008

Volltextzugriff (PDF)

Characterization of covalent inhibitors that disrupt the interaction between the tandem SH2 domains of SYK and FCER1G phospho-ITAM

PloS one, 2024-01, Vol.19 (2), p.e0293548

2024

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Food Chains: From Farmyard to Shopping Cart

1, 2010

Volltextzugriff (PDF)

Parental Perceptions of Participation in the Special Education Process

Williams, Andrew C

2016

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ChemInform Abstract: An Alternative Strategy to the Pictet-Spengler Method for Tetrahydroisoquinoline Synthesis: A Feasibility Study

ChemInform, 2012-11, Vol.43 (48), p.no-no

2012

Volltextzugriff (PDF)

ChemInform Abstract: Optimized Conditions for Styrene Syntheses Using Suzuki-Miyaura Couplings and Catalyst-Ligand-Base Pre-Mixes

ChemInform, 2012-11, Vol.43 (47), p.no-no

2012

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ChemInform Abstract: An Acid-Catalyzed Hydroamination Approach to Isoindolines

ChemInform, 2012-10, Vol.43 (43), p.no-no

2012

Volltextzugriff (PDF)

First organophosphorus radical-mediated cyclisations to afford medium-sized rings: eight-membered lactones and seven- and eight-membered lactams

Tetrahedron letters, 2005-06, Vol.46 (23), p.4027-4030

2005

Volltextzugriff (PDF)

The synthesis of carbocyclic aromatic systems

Contemporary organic synthesis, 1996, Vol.3 (6), p.535

Williams, Andrew C.

1996

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Sazetidine-A Is a Potent and Selective Agonist at Native and Recombinant Î±4Î²2 Nicotinic Acetylcholine Receptors

Molecular pharmacology, 2008-06, Vol.73 (6), p.1838

2008

Volltextzugriff (PDF)

A versatile protocol for the preparation of substituted 1- and 2-naphthyl piperazines from aminonaphthols

Tetrahedron letters, 2005-11, Vol.46 (45), p.7769-7771

2005

Volltextzugriff (PDF)

Synthetic applications of Group V metallacyclopropenes. Part 1. Group V metallacyclopropenes in synthesis. An efficient route to polyfunctional ring systems via the cocyclization of diynes with substituted monoacetylenes

Organometallics, 1989-06, Vol.8 (6), p.1566-1567

1989

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Synthesis of N-protected amino esters via palladium catalysed allylic substitution

Tetrahedron letters, 1993-10, Vol.34 (41), p.6619-6622

1993

Volltextzugriff (PDF)

Synthesis of Enantiomerically Enriched α-Amino Acid Derivatives via Transition Metal Catalysed Procedures

Synlett, 1995-08, Vol.1995 (8), p.821-822

1995

Volltextzugriff (PDF)

1 – 25 von 5.259

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Characterization of covalent inhibitors that disrupt the interaction between the tandem SH2 domains of SYK and FCER1G phospho-ITAM

Advancements in high-resolution 3D microscopy analysis of endosomal morphology in postmortem Alzheimer's disease brains

Pharmacologic enhancement of retromer rescues endosomal pathology induced by defects in the Alzheimer’s gene SORL1

The role of glucose in supporting motility and capacitation in human spermatozoa

Altmetrics, huh?

The war on error

Sazetidine-A is a potent and selective agonist at native and recombinant alpha 4 beta 2 nicotinic acetylcholine receptors

An alternative strategy to the Pictet–Spengler method for tetrahydroisoquinoline synthesis: a feasibility study

Optimised conditions for styrene syntheses using Suzuki–Miyaura couplings and catalyst-ligand-base pre-mixes

Selenocyclisations of homoallylic sulfonamides: stereoselective methods for the elaboration of substituted pyrrolidines, pyrrolines and derivatives

Acylnitrilium ion-initiated heteroannulations in alkaloid synthesis. An efficient, stereocontrolled, total synthesis of the Orchidaceae alkaloid (.+-.)-dendrobine

Sazetidine-A Is a Potent and Selective Agonist at Native and Recombinant α4β2 Nicotinic Acetylcholine Receptors

Characterization of covalent inhibitors that disrupt the interaction between the tandem SH2 domains of SYK and FCER1G phospho-ITAM

Food Chains: From Farmyard to Shopping Cart

Parental Perceptions of Participation in the Special Education Process

ChemInform Abstract: An Alternative Strategy to the Pictet-Spengler Method for Tetrahydroisoquinoline Synthesis: A Feasibility Study

ChemInform Abstract: Optimized Conditions for Styrene Syntheses Using Suzuki-Miyaura Couplings and Catalyst-Ligand-Base Pre-Mixes

ChemInform Abstract: An Acid-Catalyzed Hydroamination Approach to Isoindolines

First organophosphorus radical-mediated cyclisations to afford medium-sized rings: eight-membered lactones and seven- and eight-membered lactams

The synthesis of carbocyclic aromatic systems

Sazetidine-A Is a Potent and Selective Agonist at Native and Recombinant Î±4Î²2 Nicotinic Acetylcholine Receptors

A versatile protocol for the preparation of substituted 1- and 2-naphthyl piperazines from aminonaphthols

Synthetic applications of Group V metallacyclopropenes. Part 1. Group V metallacyclopropenes in synthesis. An efficient route to polyfunctional ring systems via the cocyclization of diynes with substituted monoacetylenes

Synthesis of N-protected amino esters via palladium catalysed allylic substitution

Synthesis of Enantiomerically Enriched α-Amino Acid Derivatives via Transition Metal Catalysed Procedures

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