Computational Studies of Pericyclic Reactions between Aminoalanes and Ethyne, Ethene, and Dienes. A Reactive Aminoalane That Should Prefer [2 + 2] and [4 + 2] Cyclizations to Dimerization-Reference-Cited by-同舟云学术

Computational Studies of Pericyclic Reactions between Aminoalanes and Ethyne, Ethene, and Dienes. A Reactive Aminoalane That Should Prefer [2 + 2] and [4 + 2] Cyclizations to Dimerization

Published:2009-01-09 Issue:3 Volume:28 Page:787-794
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Bailey John M.¹,Check Catherine E.¹,Gilbert Thomas M.¹

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/om800515e

Reference35 articles.

1. σ- and π-Bond Strengths in Main Group 3−5 Compounds

2. π-Bonding and the Lone Pair Effect in Multiple Bonds between Heavier Main Group Elements

3. Multiple Bonding Involving the Heavier Main Group 3 Elements Al, Ga, In, and Tl

4. Pericyclic Reactions between Aminoboranes R2BNR2‘ and Alkenes: [4+2] vs [2+2] Transition States

5. Ab Initio Studies of Pericyclic Reactions of Aminoboranes. [2 + 2] Dimerization and [4 + 2] Diels−Alder Reactions of H2BNH2, Me2BNMe2, and (F3C)2BNMe2

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