CASSCF Calculations Reveal Competitive Chair (Pericyclic) and Boat (Pseudopericyclic) Transition States for the [3,3] Sigmatropic Rearrangement of Allyl Esters
Author:
Affiliation:
1. Department of Chemistry, Lewis & Clark College, Portland, Oregon 97219-7899, United States
Funder
Lewis-Clark State College
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b02316
Reference37 articles.
1. Pericyclic Reaction Transition States: Passions and Punctilios, 1935-1995
2. Reaction mechanisms: pericyclic reactions
3. Pericyclic [4+2] and [3+2] Cycloaddition Reactions of Nitroarenes in Heterocyclic Synthesis
4. Pericyclic reactions in the synthesis of natural products
5. [5 + 2] Cycloaddition Reactions in Organic and Natural Product Synthesis
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1. Microwave‐Assisted 1,3‐Dioxa‐[3,3]‐Sigmatropic Rearrangement of Substituted Allylic Carbamates: Application to the Synthesis of Novel 1,3‐Oxazine‐2,4‐dione Derivatives;European Journal of Organic Chemistry;2021-11-19
2. Tracking the Transition from Pericyclic to Pseudopericyclic Reaction Mechanisms Using Multicenter Electron Delocalization Analysis: The [1,3] Sigmatropic Rearrangement;The Journal of Physical Chemistry A;2021-09-11
3. 1,3-Dioxa-[3,3]-sigmatropic Oxo-Rearrangement of Substituted Allylic Carbamates: Scope and Mechanistic Studies;The Journal of Organic Chemistry;2018-11-20
4. Evidence for a Sigmatropic and an Ionic Pathway in the Winstein Rearrangement;The Journal of Organic Chemistry;2018-06-05
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