A β,β-shielded vinyllithium example for a quantification of structure, monomer-dimer equilibrium, and some reactivity parameters
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference86 articles.
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1. β-Shielded Michael systems whose H–C(sp2) deprotonation and 1,2-addition reactions compete for organolithiums;Tetrahedron;2018-12
2. 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
3. Carbolithiation of Chloro-Substituted Alkynes: A New Access to Vinyl Carbenoids;Chemistry - A European Journal;2014-07-17
4. Carbenoid-mediated nucleophilic “hydrolysis” of 2-(dichloromethylidene)-1,1,3,3-tetramethylindane with DMSO participation, affording access to one-sidedly overcrowded ketone and bromoalkene descendants§;Beilstein Journal of Organic Chemistry;2014-01-31
5. Mixed AggregAte (MAA): A Single Concept for All Dipolar Organometallic Aggregates. 1. Structural Data;Chemical Reviews;2013-08-16
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