Copper-catalysed meso-bislactone ring opening using Grignard and mixed triorganozinc reagents
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference32 articles.
1. A Concise Account of Recent SN2′ Grignard Coupling Reactions in Organic Synthesis
2. 1,2-Asymmetric induction in the SN2'-allylation of organocopper and organozinc reagents
3. Iterative Deoxypropionate Synthesis Based on a Copper-Mediated Directed Allylic Substitution
4. Diastereoselective Reactions of δ-Oxy-Substituted Allylic Acetates with Organocopper Reagents
5. Auxiliary-based, asymmetric SN2' reactions: a case of 1,7-relative stereogenesis
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2. Reactivities of mixed organozinc and mixed organocopper reagents. Part 13 Kinetic study for phosphine-catalyzed acylation of alkylarylzincs and effect of residual group on the transfer rate of alkyl group;Journal of Physical Organic Chemistry;2016-01-19
3. Reactivity of mixed organozinc and mixed organocopper reagents: 12 . Three component reaction of mixed (n-alkyl)(diaryl)zincates, chloroformates and phosphines for the synthesis of esters;Journal of Organometallic Chemistry;2015-12
4. Single‐step oxidative homocoupling of aryl Grignard reagents via Co(II), Ni(II) and Cu(II) Complexes under air;Applied Organometallic Chemistry;2014-04-22
5. Reactivities of mixed organozinc and mixed organocopper reagents: 9. Solvent dependence of group transfer selectivity in sp3C coupling and acylation of mixed diorganocuprates and diorganozincs;Journal of Organometallic Chemistry;2013-11
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