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Accessing Indenoazulenes via a Gold‐Catalysed Cyclisation of Cycloheptatrienyl‐Substituted 1,5‐Diynes

Advanced synthesis & catalysis, 2024-03, Vol.366 (6), p.1331-1340

2024

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Gold-catalysed synthesis of phosphonate-substituted oxetan-3-ones – an easy access to highly strained HWE reagents

Organic Chemistry Frontiers, 2021-12, Vol.9 (1), p.117-122

2021

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gem-Diprenylation of Acylphloroglucinols by a Fungal Prenyltransferase of the Dimethylallyltryptophan Synthase Superfamily

Organic letters, 2017-01, Vol.19 (2), p.388-391

2017

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Stereoselective Synthesis of cis,cis-Configured Vicinal Triamines

European journal of organic chemistry, 2014-09, Vol.2014 (26), p.5749-5756

2014

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Stereoselective Synthesis of cis,cis-Configured Perhydroquinoxaline-5-Carbonitrile from Cyclohex-2-en-1-ol

Journal of heterocyclic chemistry, 2016-03, Vol.53 (2), p.533-536

2016

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Heck Reaction as Key Step in the Synthesis of Hydrogenated 2‐benzazepin‐1‐ones

Journal of heterocyclic chemistry, 2016-09, Vol.53 (5), p.1488-1493

2016

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Studies on the Enantiomers of RC-33 as Neuroprotective Agents: Isolation, Configurational Assignment, and Preliminary Biological Profile

Chirality (New York, N.Y.), 2013-11, Vol.25 (11), p.814-822

2013

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Bromolactamization: Key Step in the Stereoselective Synthesis of Enantiomerically Pure, cis-Configured Perhydropyrroloquinoxalines

Chirality (New York, N.Y.), 2014-12, Vol.26 (12), p.793-800

2014

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Molecular structure of a brominated 2-benzazepinone – a crucial intermediate in the synthesis of novel chemokine CCR2 receptor antagonists

Zeitschrift für Naturforschung. B, A journal of chemical sciences, 2017-06, Vol.72 (6), p.421-424

2017

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Investigation of the Corey Bromolactamization with N-Functionalized Allylamines

Journal of heterocyclic chemistry, 2016-11, Vol.53 (6), p.1827-1837

2016

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Structure–affinity relationship studies of non-competitive NMDA receptor antagonists derived from dexoxadrol and etoxadrol

Bioorganic & medicinal chemistry, 2005-12, Vol.13 (24), p.6836-6849

2005

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Synthesis of Thiophene-Based TAK-779 Analogues by C–H Arylation

Journal of organic chemistry, 2013-06, Vol.78 (11), p.5579-5586

2013

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Synthesis and structure/NMDA receptor affinity relationships of 1-substituted tetrahydro-3-benzazepines

Bioorganic & medicinal chemistry, 2004-03, Vol.12 (6), p.1439-1451

2004

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Improvement of σ1 receptor affinity by late-stage C–H-bond arylation of spirocyclic lactones

Bioorganic & medicinal chemistry, 2013-04, Vol.21 (7), p.1844-1856

2013

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Thiophene bioisosteres of GluN2B selective NMDA receptor antagonists: Synthesis and pharmacological evaluation of [7]annuleno[b]thiophen-6-amines

Bioorganic & medicinal chemistry, 2020-01, Vol.28 (2), p.115245, Article 115245

2020

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Chiral, nonracemic (piperazin-2-yl)methanol derivatives with σ-receptor affinity

Bioorganic & medicinal chemistry, 2004-06, Vol.12 (12), p.3299-3311

2004

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Oxetanyl Amino Acids for Peptidomimetics

Organic letters, 2017-05, Vol.19 (10), p.2510-2513

2017

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Synthesis and pharmacological evaluation of like- and unlike-configured tetrahydro-2-benzazepines with the α-substituted benzyl moiety in the 5-position

Organic & biomolecular chemistry, 2014-08, Vol.12 (29), p.5407-5426

2014

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Synthesis, GluN2B affinity and selectivity of benzo[7]annulen-7-amines

Bioorganic & medicinal chemistry, 2014-12, Vol.22 (23), p.6638-6646

2014

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Stereochemistry of the Levy Reaction

European journal of organic chemistry, 2018-12, Vol.2018 (45), p.6297-6303

2018

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Synthesis of Substituted 1‐Alkylidenephthalanes via Lithium‐Promoted 5‐exo‐dig Cyclization

European journal of organic chemistry, 2018-04, Vol.2018 (15), p.1806-1812

2018

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2-Methyltetrahydro-3-benzazepin-1-ols – The missing link in SAR of GluN2B selective NMDA receptor antagonists

Bioorganic & medicinal chemistry, 2018-01, Vol.26 (2), p.501-508

2018

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Replacement of benzylic hydroxy group by vinyl or hydroxymethyl moiety at the 3-benzazepine scaffold retaining GluN2B affinity

Bioorganic & medicinal chemistry, 2017-10, Vol.25 (20), p.5365-5372

2017

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Role of the phenolic OH moiety of GluN2B-selective NMDA antagonists with 3-benzazepine scaffold

Bioorganic & medicinal chemistry letters, 2016-02, Vol.26 (3), p.889-893

2016

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Lipase-Catalyzed Kinetic Resolution of 2-Phenylethanol Derivatives and Chiral Oxa-Pictet-Spengler Reaction as the Key Steps in the Synthesis of Enantiomerically Pure Tricyclic Amines

European journal of organic chemistry, 2012-04, Vol.2012 (12), p.2428-2444

2012

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Accessing Indenoazulenes via a Gold‐Catalysed Cyclisation of Cycloheptatrienyl‐Substituted 1,5‐Diynes

Gold-catalysed synthesis of phosphonate-substituted oxetan-3-ones – an easy access to highly strained HWE reagents

gem-Diprenylation of Acylphloroglucinols by a Fungal Prenyltransferase of the Dimethylallyltryptophan Synthase Superfamily

Stereoselective Synthesis of cis,cis-Configured Vicinal Triamines

Stereoselective Synthesis of cis,cis-Configured Perhydroquinoxaline-5-Carbonitrile from Cyclohex-2-en-1-ol

Heck Reaction as Key Step in the Synthesis of Hydrogenated 2‐benzazepin‐1‐ones

Studies on the Enantiomers of RC-33 as Neuroprotective Agents: Isolation, Configurational Assignment, and Preliminary Biological Profile

Bromolactamization: Key Step in the Stereoselective Synthesis of Enantiomerically Pure, cis-Configured Perhydropyrroloquinoxalines

Molecular structure of a brominated 2-benzazepinone – a crucial intermediate in the synthesis of novel chemokine CCR2 receptor antagonists

Investigation of the Corey Bromolactamization with N-Functionalized Allylamines

Structure–affinity relationship studies of non-competitive NMDA receptor antagonists derived from dexoxadrol and etoxadrol

Synthesis of Thiophene-Based TAK-779 Analogues by C–H Arylation

Synthesis and structure/NMDA receptor affinity relationships of 1-substituted tetrahydro-3-benzazepines

Improvement of σ1 receptor affinity by late-stage C–H-bond arylation of spirocyclic lactones

Thiophene bioisosteres of GluN2B selective NMDA receptor antagonists: Synthesis and pharmacological evaluation of [7]annuleno[b]thiophen-6-amines

Chiral, nonracemic (piperazin-2-yl)methanol derivatives with σ-receptor affinity

Oxetanyl Amino Acids for Peptidomimetics

Synthesis and pharmacological evaluation of like- and unlike-configured tetrahydro-2-benzazepines with the α-substituted benzyl moiety in the 5-position

Synthesis, GluN2B affinity and selectivity of benzo[7]annulen-7-amines

Stereochemistry of the Levy Reaction

Synthesis of Substituted 1‐Alkylidenephthalanes via Lithium‐Promoted 5‐exo‐dig Cyclization

2-Methyltetrahydro-3-benzazepin-1-ols – The missing link in SAR of GluN2B selective NMDA receptor antagonists

Replacement of benzylic hydroxy group by vinyl or hydroxymethyl moiety at the 3-benzazepine scaffold retaining GluN2B affinity

Role of the phenolic OH moiety of GluN2B-selective NMDA antagonists with 3-benzazepine scaffold

Lipase-Catalyzed Kinetic Resolution of 2-Phenylethanol Derivatives and Chiral Oxa-Pictet-Spengler Reaction as the Key Steps in the Synthesis of Enantiomerically Pure Tricyclic Amines

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