Microsolvation, Dimerization, and sp2-Stereoinversion of Monomeric α-(2,6-Diisopropylphenyl)vinyllithium
Author:
Affiliation:
1. Department Chemie, Ludwig-Maximilians-Universität, Butenandtstrasse 5-13, 81377 München, Germany
Funder
Deutsche Forschungsgemeinschaft
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om5010995
Reference19 articles.
1. Role of Organolithium Aggregates and Mixed Aggregates in Organolithium Mechanisms
2. Lithium Compounds in Organic Synthesis
3. Pseudomonomolecular, Ionic sp2-Stereoinversion Mechanism of 1-Aryl-1-alkenyllithiums
4. Microsolvation and sp2-stereoinversion of monomeric α-(2,6-di-tert-butylphenyl)vinyllithium as measured by NMR
5. Entropies of Organolithium Aggregation Based on Measured Microsolvation Numbers
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2. “Conducted Tour” Migration of Li+ during the cis /trans Stereoinversion of α-Arylvinyllithiums;Chemistry - A European Journal;2017-08-18
3. Doubly Diastereoconvergent Preparation and Microsolvation-Controlled Properties of (Z)- and (E)-1′-Lithio-1′-(2,6-dimethylphenyl)propenes;Journal of the American Chemical Society;2017-03-27
4. Kinetics of α-(2,6-Dimethylphenl)vinyllithium: How To Control Errors Caused by Inefficient Mixing with Pairs of Rapidly Competing Ketones;The Journal of Organic Chemistry;2017-02-24
5. What can 13C and 1H NMR lithiation shifts tell us about the charge distribution in α-arylvinyllithium compounds?;Journal of Organometallic Chemistry;2016-12
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