Computational Studies of the Origin of Regiospecificity in the [4+2] Diels−Alder Reaction between R2BNR2‘ Compounds and Substituted cis-Butadienes
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, Northern Illinois University, DeKalb, Illinois 60115
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om030356u
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3. Ab Initio Studies of Pericyclic Reactions of Aminoboranes. [2 + 2] Dimerization and [4 + 2] Diels−Alder Reactions of H2BNH2, Me2BNMe2, and (F3C)2BNMe2
4. Ab Initio Computational Studies of Heterocycloalkynes: Structures, Natural Bond Orders, Ring Strain Energies, and Isomerizations of Cyclic Iminoboranes and Iminoalanes
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4. Six-membered Rings with Two or More Heteroatoms with at least One Boron;Comprehensive Heterocyclic Chemistry III;2008
5. Computational Prediction of Regiospecificity in the [4+2] Diels−Alder Cyclizations between the Iminoborane (F3C)3C−B⋮N−(t-Bu) and Substituted cis-Butadienes;Organometallics;2005-11-05
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