Electrochemical reduction of the stereoisomeric 2,4-dibromopentanes to cyclopropanes. Evidence for a stepwise mechanism
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Mechanism of carbon-halogen bond cleavage. III. Electrochemical preparation of highly strained hydrocarbons
2. Electrochemical preparation of small ring compounds II, mechanism of carbon-halogen bond cleavage
3. Electrochemical preparation of bicyclobutanes and other strained cycloalkanes
4. Are nucleophilic bimolecular concerted reactions involving four or more bonds a myth?
5. The meso and Racemic Forms of 2,4-Pentanediol and Certain of Their Derivatives
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1. Electrochemistry of the Carbon-Halogen Bond;PATAI'S Chemistry of Functional Groups;2009-12-15
2. Catalytic Reduction of 1,6-Dihalohexanes by Nickel(I) Salen Electrogenerated at Glassy Carbon Cathodes in Dimethylformamide;Journal of The Electrochemical Society;2005
3. Controlled-Potential Electrolytic Reduction: 1,1-Bis(bromomethyl)cyclopropane;Organic Syntheses;2003-04-28
4. Reductive cyclizations at the cathode;Topics in Current Chemistry;1997
5. Structural Effects in Organic Electrochemistry;Topics in Organic Electrochemistry;1986
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