Differentially Protected Glycols from α‐Halo Boronic Esters and Lithiated Benzoates
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Differentially Protected Glycols from α‐Halo Boronic Esters and Lithiated Benzoates ; day:13 ; month:12 ; year:2023 ; extent:7
European journal of organic chemistry ; (13.12.2023) (gesamt 7)
- DOI
-
10.1002/ejoc.202300953
- URN
-
urn:nbn:de:101:1-2023121414102986657414
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:31 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)
Stereodivergent Olefination of Enantioenriched Boronic Esters
Stereodivergent Olefination of Enantioenriched Boronic Esters
Visible‐Light‐Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ‐Amino Boronic Esters
Visible‐Light‐Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ‐Amino Boronic Esters
Ni-Catalyzed Alkyne Cycloaddition to Give Boronic Esters
Synthesis of Boronic Ester γ‐Lactam Building Blocks
Construction of Quaternary Stereogenic Centers from Tertiary Boronic Esters
Mechanochemical Synthesis of α ‐halo Alkylboronic Esters
Desymmetrization of C2-Symmetric Bis(Boronic Esters) by Zweifel Olefinations
Insulin Delivery Using Dynamic Covalent Boronic Acid/Ester‐Controlled Release
Synthesis of Dysoxylactam A Using Iterative Homologation of Boronic Esters
Fast and efficient copper-mediated 18F-fluorination of arylstannanes, aryl boronic acids, and aryl boronic esters without azeotropic drying
Stereodivergent Olefination of Enantioenriched Boronic Esters
Stereodivergent Olefination of Enantioenriched Boronic Esters
Visible‐Light‐Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ‐Amino Boronic Esters
Visible‐Light‐Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ‐Amino Boronic Esters
Ni-Catalyzed Alkyne Cycloaddition to Give Boronic Esters
Synthesis of Boronic Ester γ‐Lactam Building Blocks
Construction of Quaternary Stereogenic Centers from Tertiary Boronic Esters
Mechanochemical Synthesis of α ‐halo Alkylboronic Esters
Desymmetrization of C2-Symmetric Bis(Boronic Esters) by Zweifel Olefinations
Insulin Delivery Using Dynamic Covalent Boronic Acid/Ester‐Controlled Release
Synthesis of Dysoxylactam A Using Iterative Homologation of Boronic Esters
Fast and efficient copper-mediated 18F-fluorination of arylstannanes, aryl boronic acids, and aryl boronic esters without azeotropic drying
Stereodivergent Olefination of Enantioenriched Boronic Esters
Stereodivergent Olefination of Enantioenriched Boronic Esters
Visible‐Light‐Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ‐Amino Boronic Esters
Visible‐Light‐Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ‐Amino Boronic Esters
Ni-Catalyzed Alkyne Cycloaddition to Give Boronic Esters
Synthesis of Boronic Ester γ‐Lactam Building Blocks
Construction of Quaternary Stereogenic Centers from Tertiary Boronic Esters
Mechanochemical Synthesis of α ‐halo Alkylboronic Esters
Desymmetrization of C2-Symmetric Bis(Boronic Esters) by Zweifel Olefinations
Insulin Delivery Using Dynamic Covalent Boronic Acid/Ester‐Controlled Release
Synthesis of Dysoxylactam A Using Iterative Homologation of Boronic Esters