Microsolvation, aggregation, and pseudomonomolecular, ionic sp2-stereoinversion mechanism of two exocyclic β,β-di-tert-alkyl-α-arylvinyllithiums-Reference-Cited by-同舟云学术

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Microsolvation, aggregation, and pseudomonomolecular, ionic sp2-stereoinversion mechanism of two exocyclic β,β-di-tert-alkyl-α-arylvinyllithiums

Published:2014-09 Issue: Volume:767 Page:125-135
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:en
Short-container-title:Journal of Organometallic Chemistry

Author:

Knorr Rudolf,Hennig Karsten-Olaf,Böhrer Petra,Schubert Bernhard

Funder

Deutsche Forschungsgemeinschaft

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference18 articles.

1. Microsolvation and 13C−Li NMR Coupling

2. Entropies of Organolithium Aggregation Based on Measured Microsolvation Numbers

3. Dynamics of Solvent Exchange in Organolithium Reagents. Lithium as a Center of Chirality1

4. Influence of Tetrahydrofuran on Reactivity, Aggregation, and Aggregate Structure of Dimethylcuprates in Diethyl Ether

5. Dynamics inside ion pairs. NMR studies of a [1-silylallyl]lithium with a pendant ligand: [1-[[[bis(2-methoxyethyl)amino]methyl]dimethylsilyl]allyl]lithium

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Organometallic Complexes of the Alkali Metals;Comprehensive Organometallic Chemistry IV;2022

2. Nickel‐Catalyzed Anionic Cross‐Coupling Reaction of Lithium Sulfonimidoyl Alkylidene Carbenoids With Organolithiums;Chemistry – A European Journal;2020-02-20

3. Why is cis / trans stereoinversion with Li + (THF) 4 migration across the phenyl ring of α-lithiostyrene accelerated by two ortho -methyl groups?;Tetrahedron;2018-04

4. “Conducted Tour” Migration of Li+ during the cis /trans Stereoinversion of α-Arylvinyllithiums;Chemistry - A European Journal;2017-08-18

5. 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

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