Detail page

Knowledge Web

Person

Daniel B. Werz (1975-)

Chemiker

Name	Daniel B. Werz
Time	1975- (Date of birth and death)
Place	Heidelberg (Geburtsort) Braunschweig (Wirkungsort) Deutschland
Academic degree	Prof. Dr. Habil. (Universität Göttingen) (2011) Dr. (Universität Heideleberg) (2003) Dipl. (Universität Heidelberg) (2000)
Profession	Chemiker (characteristic profession)
Variant	Daniel Werz Daniel Bodo Werz
Related	Albert-Ludwigs-Universität Freiburg (2022-) Institut für Organische Chemie (Braunschweig) (2013-2022) Georg-August-Universität Göttingen (2006-2012) Eidgenössische Technische Hochschule Zürich (2004-2006) Organisch-Chemisches Institut (Heidelberg) (2000-2003)
Source	Homepage: https://www.werzlab.de/ (Stand: 25.05.2023) Wikipedia: https://de.wikipedia.org/wiki/Daniel_B._Werz (Stand: 25.05.2023)
Record type	Person
GND-Identifier	1141094398
Record ID	1141094398
Involved in show all A BOIMPY Dye Enables Multi‐Photoinduced Electron Transfer Catalysis: Reaching Super‐Reducing Properties A BOIMPY Dye Enables Multi‐Photoinduced Electron Transfer Catalysis: Reaching Super‐Reducing Properties A BOIMPY dye enables multi‐photoinduced electron transfer catalysis: reaching super‐reducing properties Double strain‐release (3+3)‐cycloaddition: Lewis acid catalyzed reaction of bicyclobutane carboxylates and aziridines Double Strain‐Release (3+3)‐Cycloaddition: Lewis Acid Catalyzed Reaction of Bicyclobutane Carboxylates and Aziridines Ring‐Opening Reactions of Donor‐Acceptor Cyclopropanes with Enolizable 5‐Mercapto‐1 H ‐tetrazoles Deuteration and Tritiation of Pharmaceuticals by Non‐Directed Palladium‐Catalyzed C−H Activation in Heavy and Super‐Heavy Water Deuteration and Tritiation of Pharmaceuticals by Non‐Directed Palladium‐Catalyzed C−H Activation in Heavy and Super‐Heavy Water Correspondence on “Organo‐Mediator Enabled Electrochemical Deuteration of Styrenes” Correspondence on “Organo‐Mediator Enabled Electrochemical Deuteration of Styrenes” Phenylazo-BODIPYs: Direct Access via Pd-Catalysis Rational Design of Fluorophores Using MO Theory: Our Journey from BODIPYs to BOIMPYs Water‐Soluble Fluorescent Polymer Dyes with Tunable Emission Spectra for Flow Cytometry Applications Water‐Soluble Fluorescent Polymer Dyes with Tunable Emission Spectra for Flow Cytometry Applications Electrochemical Diselenation of BODIPY Fluorophores for Bioimaging Applications and Sensitization of 1 O 2 Electrochemical Diselenation of BODIPY Fluorophores for Bioimaging Applications and Sensitization of 1 O 2 Electrochemical Diselenation of BODIPY Fluorophores for Bioimaging Applications and Sensitization of 1 O 2 Diastereoselective (8+3)‐Cycloadditions of Donor‐Acceptor Cyclopropanes with Tropothione Deuteration and tritiation of pharmaceuticals by non‐directed palladium‐catalyzed C−H activation in heavy and super‐heavy water Rational design of fluorophores using mo theory: our journey from BODYPs to BIOMPYs Electrocatalytic Synthesis of 1,2-Dioxolanes from Tetrasubstituted Donor–Acceptor Cyclopropanes Site‐selective Hydrogenation/Deuteration of Benzylic Olefins Enabled by Electroreduction Using Water A Widely Applicable and Versatile Method for the Ring‐Opening 1,3‐Carbocarbonation of Donor‐Acceptor Cyclopropanes A widely applicable and versatile method for the ring‐opening 1,3‐carbocarbonation of donor‐acceptor cyclopropanes Access to isoindole-derived BODIPYs by an aminopalladation cascade Aminopalladierungskaskaden zum Aufbau Stickstoff-haltiger Heterozyklen und BODIPY-Kernstrukturen Development of artificial siderophores, antibacterial drugs and siderophore-drug conjugates against pathogenic bacteria Electrochemical activation of strained donor-acceptor substituted carbocycles and selective hydrogenation of benzylic olefins by electroreduction Erweiterung des Spektrums von Donor-Akzeptor Cyclopropanen Highly scalable photoinduced synthesis of silanols via untraversed pathway for chlorine radical (Cl.) generation Organochalkogene in Reactionen mit Donor-Akzeptor Cyclopropanen: (3+1)- und (3+2)-Cycloadditionen Reactions of donor-acceptor cyclopropanes with chalcogen- and pnictogen-rich species Site‐selective hydrogenation/eeuteration of benzylic olefins enabled by electroreduction using water Untersuchungen zur Totalsynthese der Calyculone Donor‐Acceptor Cyclopropanes: Activation Enabled by a Single, Vinylogous Acceptor Donor‐Acceptor Cyclopropanes: Activation Enabled by a Single, Vinylogous Acceptor Optical Manipulation of Gb 3 Enriched Lipid Domains: Impact of Isomerization on Gb 3 ‐Shiga Toxin B Interaction Transforming Dyes into Fluorophores: Exciton‐Induced Emission with Chain‐like Oligo‐BODIPY Superstructures Transforming Dyes into Fluorophores: Exciton‐Induced Emission with Chain‐like Oligo‐BODIPY Superstructures Fluorescent π-Conjugated Polymer Dyes for Flow Cytometry Formal insertion of selenoketenes into donor–acceptor cyclopropanes: mesomeric alkynylselenolates as key starting materials Thermodynamisch kontrollierte Atropisomerie in makrocyclisch verbrückten 2-Arylpyridin-N-oxiden, 2-(2’-Phosphinoaryl)pyridinen und 2,2’-Bis(diphenylphosphino)-1,1’-biphenylen für die Anwendung in der asymmetrischen Katalyse Cycloadditions of Donor–Acceptor Cyclopropanes and ‐butanes using S=N‐Containing Reagents: Access to Cyclic Sulfinamides, Sulfonamides, and Sulfinamidines Cycloadditions of Donor–Acceptor Cyclopropanes and ‐butanes using S=N‐Containing Reagents: Access to Cyclic Sulfinamides, Sulfonamides, and Sulfinamidines Alkyne Aminopalladation/Heck and Suzuki Cascades: An Approach to Tetrasubstituted Enamines Azide⋅⋅⋅Oxygen Interaction: A Crystal Engineering Tool for Conformational Locking Azide⋅⋅⋅Oxygen Interaction: A Crystal Engineering Tool for Conformational Locking Lewis‐Acid‐Catalyzed (3+2)‐Cycloadditions of Donor‐Acceptor Cyclopropanes with Thioketenes Electrocatalytic Activation of Donor–Acceptor Cyclopropanes and Cyclobutanes: An Alternative C(sp 3 )−C(sp 3 ) Cleavage Mode Electrocatalytic Activation of Donor–Acceptor Cyclopropanes and Cyclobutanes: An Alternative C(sp 3 )−C(sp 3 ) Cleavage Mode Azide‐Functionalized Derivatives of the Virulence‐Associated Sugar Pseudaminic Acid: Chiral Pool Synthesis and Labeling of Bacteria Regio‐ and Diastereoselective Copper‐Catalyzed Carbomagnesiation for the Synthesis of Penta‐ and Hexa‐Substituted Cyclopropanes Regio‐ and Diastereoselective Copper‐Catalyzed Carbomagnesiation for the Synthesis of Penta‐ and Hexa‐Substituted Cyclopropanes (3+2)-Cycloaddition of Donor–Acceptor Cyclopropanes with Thiocyanate: A Facile and Efficient Synthesis of 2-Amino-4,5-dihydrothiophenes Functionalization of Sydnones with Donor‐Acceptor Cyclopropanes, Cyclobutanes, and Michael Acceptors Quantification of Noncovalent Interactions in Azide–Pnictogen, –Chalcogen, and –Halogen Contacts GlycoBODIPYs: Sugars Serving as a Natural Stock for Water‐soluble Fluorescent Probes of Complex Chiral Morphology Protic Ionic Liquid as Reagent, Catalyst, and Solvent: 1‐Methylimidazolium Thiocyanate GlycoBODIPYs: Sugars Serving as a Natural Stock for Water‐soluble Fluorescent Probes of Complex Chiral Morphology Protic Ionic Liquid as Reagent, Catalyst, and Solvent: 1‐Methylimidazolium Thiocyanate

Please note

The beta version does not yet contain all functions and information of the DNB portal catalogue. If you are missing information or want to order a medium, please visit the page in the DNB portal catalogue via the following link:

Katalog der Deutschen Nationalbibliothek

Daniel B. Werz (1975-)

A BOIMPY Dye Enables Multi‐Photoinduced Electron Transfer Catalysis: Reaching Super‐Reducing Properties

A BOIMPY Dye Enables Multi‐Photoinduced Electron Transfer Catalysis: Reaching Super‐Reducing Properties

A BOIMPY dye enables multi‐photoinduced electron transfer catalysis: reaching super‐reducing properties

Double strain‐release (3+3)‐cycloaddition: Lewis acid catalyzed reaction of bicyclobutane carboxylates and aziridines

Double Strain‐Release (3+3)‐Cycloaddition: Lewis Acid Catalyzed Reaction of Bicyclobutane Carboxylates and Aziridines

Ring‐Opening Reactions of Donor‐Acceptor Cyclopropanes with Enolizable 5‐Mercapto‐1 H ‐tetrazoles

Deuteration and Tritiation of Pharmaceuticals by Non‐Directed Palladium‐Catalyzed C−H Activation in Heavy and Super‐Heavy Water

Deuteration and Tritiation of Pharmaceuticals by Non‐Directed Palladium‐Catalyzed C−H Activation in Heavy and Super‐Heavy Water

Correspondence on “Organo‐Mediator Enabled Electrochemical Deuteration of Styrenes”

Correspondence on “Organo‐Mediator Enabled Electrochemical Deuteration of Styrenes”

Phenylazo-BODIPYs: Direct Access via Pd-Catalysis

Rational Design of Fluorophores Using MO Theory: Our Journey from BODIPYs to BOIMPYs

Water‐Soluble Fluorescent Polymer Dyes with Tunable Emission Spectra for Flow Cytometry Applications

Water‐Soluble Fluorescent Polymer Dyes with Tunable Emission Spectra for Flow Cytometry Applications

Electrochemical Diselenation of BODIPY Fluorophores for Bioimaging Applications and Sensitization of 1 O 2

Electrochemical Diselenation of BODIPY Fluorophores for Bioimaging Applications and Sensitization of 1 O 2

Electrochemical Diselenation of BODIPY Fluorophores for Bioimaging Applications and Sensitization of 1 O 2

Diastereoselective (8+3)‐Cycloadditions of Donor‐Acceptor Cyclopropanes with Tropothione

Deuteration and tritiation of pharmaceuticals by non‐directed palladium‐catalyzed C−H activation in heavy and super‐heavy water

Rational design of fluorophores using mo theory: our journey from BODYPs to BIOMPYs

Electrocatalytic Synthesis of 1,2-Dioxolanes from Tetrasubstituted Donor–Acceptor Cyclopropanes

Site‐selective Hydrogenation/Deuteration of Benzylic Olefins Enabled by Electroreduction Using Water

A Widely Applicable and Versatile Method for the Ring‐Opening 1,3‐Carbocarbonation of Donor‐Acceptor Cyclopropanes

A widely applicable and versatile method for the ring‐opening 1,3‐carbocarbonation of donor‐acceptor cyclopropanes

Access to isoindole-derived BODIPYs by an aminopalladation cascade

Aminopalladierungskaskaden zum Aufbau Stickstoff-haltiger Heterozyklen und BODIPY-Kernstrukturen

Development of artificial siderophores, antibacterial drugs and siderophore-drug conjugates against pathogenic bacteria

Electrochemical activation of strained donor-acceptor substituted carbocycles and selective hydrogenation of benzylic olefins by electroreduction

Erweiterung des Spektrums von Donor-Akzeptor Cyclopropanen

Highly scalable photoinduced synthesis of silanols via untraversed pathway for chlorine radical (Cl.) generation

Organochalkogene in Reactionen mit Donor-Akzeptor Cyclopropanen: (3+1)- und (3+2)-Cycloadditionen

Reactions of donor-acceptor cyclopropanes with chalcogen- and pnictogen-rich species

Site‐selective hydrogenation/eeuteration of benzylic olefins enabled by electroreduction using water

Untersuchungen zur Totalsynthese der Calyculone

Donor‐Acceptor Cyclopropanes: Activation Enabled by a Single, Vinylogous Acceptor

Donor‐Acceptor Cyclopropanes: Activation Enabled by a Single, Vinylogous Acceptor

Optical Manipulation of Gb 3 Enriched Lipid Domains: Impact of Isomerization on Gb 3 ‐Shiga Toxin B Interaction

Transforming Dyes into Fluorophores: Exciton‐Induced Emission with Chain‐like Oligo‐BODIPY Superstructures

Transforming Dyes into Fluorophores: Exciton‐Induced Emission with Chain‐like Oligo‐BODIPY Superstructures

Fluorescent π-Conjugated Polymer Dyes for Flow Cytometry

Formal insertion of selenoketenes into donor–acceptor cyclopropanes: mesomeric alkynylselenolates as key starting materials

Thermodynamisch kontrollierte Atropisomerie in makrocyclisch verbrückten 2-Arylpyridin-N-oxiden, 2-(2’-Phosphinoaryl)pyridinen und 2,2’-Bis(diphenylphosphino)-1,1’-biphenylen für die Anwendung in der asymmetrischen Katalyse

Cycloadditions of Donor–Acceptor Cyclopropanes and ‐butanes using S=N‐Containing Reagents: Access to Cyclic Sulfinamides, Sulfonamides, and Sulfinamidines

Cycloadditions of Donor–Acceptor Cyclopropanes and ‐butanes using S=N‐Containing Reagents: Access to Cyclic Sulfinamides, Sulfonamides, and Sulfinamidines

Alkyne Aminopalladation/Heck and Suzuki Cascades: An Approach to Tetrasubstituted Enamines

Azide⋅⋅⋅Oxygen Interaction: A Crystal Engineering Tool for Conformational Locking

Azide⋅⋅⋅Oxygen Interaction: A Crystal Engineering Tool for Conformational Locking

Lewis‐Acid‐Catalyzed (3+2)‐Cycloadditions of Donor‐Acceptor Cyclopropanes with Thioketenes

Electrocatalytic Activation of Donor–Acceptor Cyclopropanes and Cyclobutanes: An Alternative C(sp 3 )−C(sp 3 ) Cleavage Mode

Electrocatalytic Activation of Donor–Acceptor Cyclopropanes and Cyclobutanes: An Alternative C(sp 3 )−C(sp 3 ) Cleavage Mode

Azide‐Functionalized Derivatives of the Virulence‐Associated Sugar Pseudaminic Acid: Chiral Pool Synthesis and Labeling of Bacteria

Regio‐ and Diastereoselective Copper‐Catalyzed Carbomagnesiation for the Synthesis of Penta‐ and Hexa‐Substituted Cyclopropanes

Regio‐ and Diastereoselective Copper‐Catalyzed Carbomagnesiation for the Synthesis of Penta‐ and Hexa‐Substituted Cyclopropanes

(3+2)-Cycloaddition of Donor–Acceptor Cyclopropanes with Thiocyanate: A Facile and Efficient Synthesis of 2-Amino-4,5-dihydrothiophenes

Functionalization of Sydnones with Donor‐Acceptor Cyclopropanes, Cyclobutanes, and Michael Acceptors

Quantification of Noncovalent Interactions in Azide–Pnictogen, –Chalcogen, and –Halogen Contacts

GlycoBODIPYs: Sugars Serving as a Natural Stock for Water‐soluble Fluorescent Probes of Complex Chiral Morphology

Protic Ionic Liquid as Reagent, Catalyst, and Solvent: 1‐Methylimidazolium Thiocyanate

GlycoBODIPYs: Sugars Serving as a Natural Stock for Water‐soluble Fluorescent Probes of Complex Chiral Morphology

Protic Ionic Liquid as Reagent, Catalyst, and Solvent: 1‐Methylimidazolium Thiocyanate