Direct nucleophilic and electrophilic activation of alcohols using a unified boron-based organocatalyst scaffold
Abstract Organocatalytic strategies for the direct activation of hydroxy-containing compounds have paled in comparison to those applicable to carbonyl compounds. To this end, boronic acids have emerged as valuable catalysts for the functionalization of hydroxy groups in a mild and selective fashion....
Main Authors: | Jason P. G. Rygus, Dennis G. Hall |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2023-05-01
|
Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-023-38228-8 |
Similar Items
-
Asymmetric electrophilic fluorocyclization with carbon nucleophiles.
by: Wolstenhulme, JR, et al.
Published: (2013) -
Graphene Oxide as an Electrophile for Carbon Nucleophiles
by: Swager, Timothy Manning, et al.
Published: (2012) -
Electrophilically Activated Nitroalkanes in Reactions With Carbon Based Nucleophiles
by: Nicolai A. Aksenov, et al.
Published: (2020-02-01) -
Ionic Liquids as Organocatalysts for Nucleophilic Fluorination: Concepts and Perspectives
by: Young-Ho Oh, et al.
Published: (2022-09-01) -
Analogy of the Reactions of Aromatic and Aliphatic π-Electrophiles with Nucleophiles
by: Michał Barbasiewicz, et al.
Published: (2023-05-01)