- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Synthetic Approaches to Triarylboranes from 1885 to 2020 ; year:2021
Chemistry - a European journal ; (2021)
- DOI
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10.1002/chem.202005302
- URN
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urn:nbn:de:101:1-2021030414060312534973
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
- 15.08.2025, 7:30 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
Other Objects (12)
Synthetic Approaches to Triarylboranes from 1885 to 2020
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C-H Borylation: A Route to Novel Pyrenes and Perylenes and the Investigation of their Excited States and Redox Properties
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Development of New Methods for Triarylborane Synthesis and Investigation of Triarylborane Chromophores for DNA and RNA Sensing and Singlet Oxygen Sensitization
Synthesis, group 10 metal-catalyzed cyclization reactions and hydroboration of polyynes
1,3-Bis(trifluoromethyl)benzene: A Versatile Building Block for the Synthesis of New Boron-Containing Conjugated Systems
Persistent Room‐Temperature Phosphorescence from Purely Organic Molecules and Multi‐Component Systems
Mechanistic and Kinetic Factors of ortho‐Benzyne Formation in Hexadehydro‐Diels‐Alder (HDDA) Reactions
A Very Positive Image of Boron: Triarylborane Chromophores for Live Cell Imaging
Earth-Abundant Metal-Catalyzed and Transition Metal-Free Borylation of Aryl Halides
Synthetic Approaches to Triarylboranes from 1885 to 2020
Mechanistic and Kinetic Factors of ortho ‐Benzyne Formation in Hexadehydro‐Diels‐Alder (HDDA) Reactions
Copper‐Catalyzed Borylation of Acyl Chlorides with an Alkoxy Diboron Reagent: A Facile Route to Acylboron Compounds
C-H Borylation: A Route to Novel Pyrenes and Perylenes and the Investigation of their Excited States and Redox Properties
Contemporary metal boron chemistry, 1.. Borylenes, boryls, borane _s [sigma-complexes], and borohydrides / vol. ed.: Todd B. Marder ; Zhenyang Lin. With contributions by S. Aldridge ...
Development of New Methods for Triarylborane Synthesis and Investigation of Triarylborane Chromophores for DNA and RNA Sensing and Singlet Oxygen Sensitization
Synthesis, group 10 metal-catalyzed cyclization reactions and hydroboration of polyynes
1,3-Bis(trifluoromethyl)benzene: A Versatile Building Block for the Synthesis of New Boron-Containing Conjugated Systems
Persistent Room‐Temperature Phosphorescence from Purely Organic Molecules and Multi‐Component Systems
Mechanistic and Kinetic Factors of ortho‐Benzyne Formation in Hexadehydro‐Diels‐Alder (HDDA) Reactions
A Very Positive Image of Boron: Triarylborane Chromophores for Live Cell Imaging
Earth-Abundant Metal-Catalyzed and Transition Metal-Free Borylation of Aryl Halides
Synthetic Approaches to Triarylboranes from 1885 to 2020
Mechanistic and Kinetic Factors of ortho ‐Benzyne Formation in Hexadehydro‐Diels‐Alder (HDDA) Reactions
Copper‐Catalyzed Borylation of Acyl Chlorides with an Alkoxy Diboron Reagent: A Facile Route to Acylboron Compounds
C-H Borylation: A Route to Novel Pyrenes and Perylenes and the Investigation of their Excited States and Redox Properties
Contemporary metal boron chemistry, 1.. Borylenes, boryls, borane _s [sigma-complexes], and borohydrides / vol. ed.: Todd B. Marder ; Zhenyang Lin. With contributions by S. Aldridge ...
Development of New Methods for Triarylborane Synthesis and Investigation of Triarylborane Chromophores for DNA and RNA Sensing and Singlet Oxygen Sensitization
Synthesis, group 10 metal-catalyzed cyclization reactions and hydroboration of polyynes
1,3-Bis(trifluoromethyl)benzene: A Versatile Building Block for the Synthesis of New Boron-Containing Conjugated Systems
Persistent Room‐Temperature Phosphorescence from Purely Organic Molecules and Multi‐Component Systems
Mechanistic and Kinetic Factors of ortho‐Benzyne Formation in Hexadehydro‐Diels‐Alder (HDDA) Reactions
A Very Positive Image of Boron: Triarylborane Chromophores for Live Cell Imaging