Proton Affinities of N-Heterocyclic Olefins and Their Implications for Organocatalyst Design
Author:
Affiliation:
1. Institute for Theoretical Chemistry, University of Stuttgart, Pfaffenwaldring 55, D-70569 Stuttgart, Germany
2. Institute of Polymer Chemistry, University of Stuttgart, Pfaffenwaldring 55, D-70569 Stuttgart, Germany
Funder
Deutsche Forschungsgemeinschaft
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b03202
Reference71 articles.
1. Naumann, S. In Organic Catalysis for Polymerization; Dove, A. P., Sardon, H., Naumann, S., Eds.; RSC Polymer Chemistry Series, RSC: London, 2018; Chpt. 4, pp 121–187.
2. The Resurgence of the Highly Ylidic N-Heterocyclic Olefins as a New Class of Organocatalysts
3. Fast CO2 Sequestration, Activation, and Catalytic Transformation Using N-Heterocyclic Olefins
4. CO2, COS and CS2 adducts of N-heterocyclic olefins and their application as organocatalysts for carbon dioxide fixation
5. A theoretical investigation of substituent effects on the stability and reactivity of N-heterocyclic olefin carboxylates
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