Stereochemical labeling at natural abundance. Stereochemistry, isotope effects, and mechanism of the Diels-Alder reaction of hexachlorocyclopentadiene with ethyl vinyl ether
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Mechanistic Aspects of Diels-Alder Reactions: A Critical Survey
2. a(E)-1-Methoxy-1,3-butadiene and 1,1-Dimethoxy-1,3-butadiene in (4 + 2) Cycloadditions. A Mechanistic Comparison
3. a(E)-1-Methoxy-1,3-butadiene and 1,1-Dimethoxy-1,3-butadiene in (4 + 2) Cycloadditions. A Mechanistic Comparison
4. Reactions of Alkynyldihaloboranes with 1,3-Dienes. 1,4-Alkynylborations and Stepwise Diels−Alder Reactions
5. Nonstereospecific Diels-Alder reactions. I. Reaction of hexachlorocyclopentadiene with 1,2-disubstituted ethylenes
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2. Enantioselective organocatalytic diels-Alder reactions: A density functional theory and kinetic isotope effects study;Journal of Computational Chemistry;2011-03-31
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4. Application of NMR Spectroscopy in Isotope Effects Studies;Annual Reports on NMR Spectroscopy;2009
5. Hetero-Diels-Alder and Cheletropic Additions of Sulfur Dioxide to Conjugated Dienes. Experimental Facts and Theoretical Analysis;Current Organic Chemistry;2006-11-01
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