Strain energies of gem-difluorocyclopropanes and related molecules
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. Microwave spectrum, structure, and dipole moment of 1,1‐difluorocyclopropane
2. On the electronic and molecular structures of some fluoro-substituted cyclopropane derivatives
3. Fluorocyclopropanes. III. 1,4-Cycloaddition reactions of perfluorocyclopropene and 1,2-bis(trifluoromethyl)-3,3-difluorocyclopropene
4. Cheletropic reactions of fluorocarbenes with norbornadienes
5. Thermal isomerization and fragmentation of 1,1-difluoro-2,3-dimethylcyclopropane
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1. Monosubstituted 3,3‐Difluorocyclopropenes as Bench‐Stable Reagents: Scope and Limitations;European Journal of Organic Chemistry;2021-12-04
2. Asymmetric Transfer Hydrogenation of gem ‐Difluorocyclopropenyl Esters: Access to Enantioenriched gem ‐Difluorocyclopropanes;Angewandte Chemie International Edition;2020-08-25
3. Asymmetric Transfer Hydrogenation of gem ‐Difluorocyclopropenyl Esters: Access to Enantioenriched gem ‐Difluorocyclopropanes;Angewandte Chemie;2020-08-25
4. Stereoselective Ring-Opening of gem -Difluorocyclopropanes: An Entry to Stereo-defined (E ,E )- and (E ,Z )-Conjugated Fluorodienes;Chemistry - A European Journal;2017-12-12
5. A Semi-homodesmotic Approach for Estimating Ring Strain Energies (RSEs) of Highly Substituted Cyclopropanes That Minimizes Use of Acyclic References and Cancels Steric Interactions: RSEs for c-C3R6 that Make Sense;The Journal of Physical Chemistry A;2014-07-28
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