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G{sub E{sub p}}/G{sub M{sub p}} ratio by polarization transfer in e --> p --> ep --

Physical review letters, 2000-02, Vol.84 (7)

2000

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Silicon Organic Hybrid Technology-A Platform for Practical Nonlinear Optics

Proceedings of the IEEE, 2009-07, Vol.97 (7), p.1304-1316

2009

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A Small-Molecule Inhibitor of Bax and Bak Oligomerization Prevents Genotoxic Cell Death and Promotes Neuroprotection

Cell chemical biology, 2017-04, Vol.24 (4), p.493-506.e5

2017

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One-Electron-Reduced and -Oxidized Stages of Donor-Substituted 1,1,4,4-Tetracyanobuta-1,3-dienes of Different Molecular Architectures

Chemistry : a European journal, 2008-08, Vol.14 (25), p.7638-7647

2008

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Donor-Substituted 1,1,4,4-Tetracyanobutadienes (TCBDs): New Chromophores with Efficient Intramolecular Charge-Transfer Interactions by Atom-Economic Synthesis

Chemistry : a European journal, 2006-02, Vol.12 (7), p.1889-1905

2006

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Phylogenetic insights resolve Dacampiaceae (Pleosporales) as polyphyletic: Didymocyrtis (Pleosporales, Phaeosphaeriaceae) with Phoma-like anamorphs resurrected and segregated from Polycoccum (Trypetheliales, Polycoccaceae fam. nov.)

Fungal diversity, 2015-09, Vol.74 (1), p.53-89

2015

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Comparison of CC Triple and Double Bonds as Spacers in Push-Pull Chromophores

European Journal of Organic Chemistry, 2011-08, Vol.2011 (23), p.4307-4317

2011

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A Four‐Step Synthesis of Substituted 5,11‐Dicyano‐6,12‐diaryltetracenes with Enhanced Stability and High Fluorescence Emission

Chemistry : a European journal, 2018-01, Vol.24 (1), p.159-168

2018

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Donor-Substituted Diphenylacetylene Derivatives Act as Electron Donors and Acceptors

Journal of organic chemistry, 2011-07, Vol.76 (14), p.5628-5635

2011

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1,2-Di(phenylethynyl)ethenes with axially chiral, 2,2'-bridged 1,1'-binaphthyl substituents: potent cholesteric liquid-crystal inducers

Organic & biomolecular chemistry, 2012-10, Vol.10 (39), p.8016-8026

2012

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CUGBP2 Plays a Critical Role in Apoptosis of Breast Cancer Cells in Response to Genotoxic Injury

Annals of the New York Academy of Sciences, 2003-12, Vol.1010 (1), p.504-509

2003

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Heart Failure Optimize Clinic: Improving Quality of Care In Heart Failure Patients In An Academic Medical Center

Journal of cardiac failure, 2020-10, Vol.26 (10), p.S131-S132

2020

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A new species of Synarthonia from Luxembourg, and a new combination in the genus Reichlingia (Arthoniaceae)

The Lichenologist (London), 2020-07, Vol.52 (4), p.261-266

2020

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Apoptotic cell death in disease—Current understanding of the NCCD 2023

Cell death and differentiation, 2023-04, p.1097-1154

2023

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Chiral and Achiral Charge-Transfer Chromophores with a Dendralene-Type Backbone by Electronically Controlled Cycloaddition/Cycloreversion Cascades

European Journal of Organic Chemistry, 2010-05, Vol.2010 (13), p.2487-2503

2010

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Defining the Chemotherapeutic Targets of Histone Deacetylase Inhibitors

Annals of the New York Academy of Sciences, 2004-12, Vol.1030 (1), p.627-635

2004

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1,2-Di(phenylethynyl)ethenes with axially chiral, 2,2′-bridged 1,1′-binaphthyl substituents: potent cholesteric liquid-crystal inducersElectronic supplementary information (ESI) available: Additional synthetic protocols, experimental details of photoisomerisation, UV/Vis spectral changes upon excitation, emission spectra and 1H and 13C NMR spectra of new compounds. CCDC 876925. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2ob25983d

2012-09

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Second-Generation Inhibitors for the Metalloprotease Neprilysin Based on Bicyclic Heteroaromatic Scaffolds: Synthesis, Biological Activity, and X-Ray Crystal-Structure Analysis

Helvetica chimica acta, 2005-04, Vol.88 (4), p.731-750

2005

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Cover Picture: N-Arylated 3,5-Dihydro-4H-dinaphtho[2,1-c:1′,2′-e]azepines: Axially Chiral Donors with High Helical Twisting Powers for Nonplanar Push-Pull Chromophores (Chem. Eur. J. 36/2009)

Chemistry : a European journal, 2009-09, Vol.15 (36), p.8919-8919

2009

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Cover Picture: N ‐Arylated 3,5‐Dihydro‐4 H ‐dinaphtho[2,1‐ c :1′,2′‐ e ]azepines: Axially Chiral Donors with High Helical Twisting Powers for Nonplanar Push–Pull Chromophores (Chem. Eur. J. 36/2009)

Chemistry : a European journal, 2009-09, Vol.15 (36), p.8919-8919

2009

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N ‐Arylated 3,5‐Dihydro‐4 H ‐dinaphtho[2,1‐ c :1′,2′‐ e ]azepines: Axially Chiral Donors with High Helical Twisting Powers for Nonplanar Push–Pull Chromophores

Chemistry : a European journal, 2009-09, Vol.15 (36), p.9005-9016

2009

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Silicon Organic Hybrid Technology-A Platform for Practical Nonlinear Optics: Silicon Photonics

Proceedings of the IEEE, 2009, Vol.97 (7), p.1304-1316

2009

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Fellhanera gyrophorica, a new European species with conspicuous pycnidia

The Lichenologist (London), 2001-07, Vol.33 (4), p.285-289

2001

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Generation of 1,2-Bisketenes from Cyclobutene-1,2-diones by Flash Photolysis and Ring Closure Kinetics1a

Journal of the American Chemical Society, 1997-12, Vol.119 (50), p.12125-12130

1997

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Generation of 1,2-Bisketenes from Cyclobutene-1,2-diones by Flash Photolysis and Ring Closure Kinetics J. Am. Chem. Soc. 1997, 119, 12125−12130

Journal of the American Chemical Society, 1998-09, Vol.120 (34), p.8901-8901

1998

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G{sub E{sub p}}/G{sub M{sub p}} ratio by polarization transfer in e --> p --> ep --

Silicon Organic Hybrid Technology-A Platform for Practical Nonlinear Optics

A Small-Molecule Inhibitor of Bax and Bak Oligomerization Prevents Genotoxic Cell Death and Promotes Neuroprotection

One-Electron-Reduced and -Oxidized Stages of Donor-Substituted 1,1,4,4-Tetracyanobuta-1,3-dienes of Different Molecular Architectures

Donor-Substituted 1,1,4,4-Tetracyanobutadienes (TCBDs): New Chromophores with Efficient Intramolecular Charge-Transfer Interactions by Atom-Economic Synthesis

Phylogenetic insights resolve Dacampiaceae (Pleosporales) as polyphyletic: Didymocyrtis (Pleosporales, Phaeosphaeriaceae) with Phoma-like anamorphs resurrected and segregated from Polycoccum (Trypetheliales, Polycoccaceae fam. nov.)

Comparison of CC Triple and Double Bonds as Spacers in Push-Pull Chromophores

A Four‐Step Synthesis of Substituted 5,11‐Dicyano‐6,12‐diaryltetracenes with Enhanced Stability and High Fluorescence Emission

Donor-Substituted Diphenylacetylene Derivatives Act as Electron Donors and Acceptors

1,2-Di(phenylethynyl)ethenes with axially chiral, 2,2'-bridged 1,1'-binaphthyl substituents: potent cholesteric liquid-crystal inducers

CUGBP2 Plays a Critical Role in Apoptosis of Breast Cancer Cells in Response to Genotoxic Injury

Heart Failure Optimize Clinic: Improving Quality of Care In Heart Failure Patients In An Academic Medical Center

A new species of Synarthonia from Luxembourg, and a new combination in the genus Reichlingia (Arthoniaceae)

Apoptotic cell death in disease—Current understanding of the NCCD 2023

Chiral and Achiral Charge-Transfer Chromophores with a Dendralene-Type Backbone by Electronically Controlled Cycloaddition/Cycloreversion Cascades

Defining the Chemotherapeutic Targets of Histone Deacetylase Inhibitors

Second-Generation Inhibitors for the Metalloprotease Neprilysin Based on Bicyclic Heteroaromatic Scaffolds: Synthesis, Biological Activity, and X-Ray Crystal-Structure Analysis

Cover Picture: N-Arylated 3,5-Dihydro-4H-dinaphtho[2,1-c:1′,2′-e]azepines: Axially Chiral Donors with High Helical Twisting Powers for Nonplanar Push-Pull Chromophores (Chem. Eur. J. 36/2009)

Cover Picture: N ‐Arylated 3,5‐Dihydro‐4 H ‐dinaphtho[2,1‐ c :1′,2′‐ e ]azepines: Axially Chiral Donors with High Helical Twisting Powers for Nonplanar Push–Pull Chromophores (Chem. Eur. J. 36/2009)

N ‐Arylated 3,5‐Dihydro‐4 H ‐dinaphtho[2,1‐ c :1′,2′‐ e ]azepines: Axially Chiral Donors with High Helical Twisting Powers for Nonplanar Push–Pull Chromophores

Silicon Organic Hybrid Technology-A Platform for Practical Nonlinear Optics: Silicon Photonics

Fellhanera gyrophorica, a new European species with conspicuous pycnidia

Generation of 1,2-Bisketenes from Cyclobutene-1,2-diones by Flash Photolysis and Ring Closure Kinetics1a

Generation of 1,2-Bisketenes from Cyclobutene-1,2-diones by Flash Photolysis and Ring Closure Kinetics J. Am. Chem. Soc. 1997, 119, 12125−12130

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