2002
DOI: 10.1002/chin.200251030
|View full text |Cite
|
Sign up to set email alerts
|

Acylotropic Tautomerism. Part 35. R⇔L‐Inversion of Configuration of Dipolar Spirocyclic and Open‐Chain 2‐Arylaminotropone Isomers.

Abstract: 2002 stereochemistry stereochemistry (general, optical resolution) O 0030 -030Acylotropic Tautomerism. Part 35. R⇔L-Inversion of Configuration of Dipolar Spirocyclic and Open-Chain 2-Arylaminotropone Isomers.-The R⇔L inversion of the configuration of various spirocyclic arylaminotropone derivatives (I)-(IV) is studied using dynamic NMR technique. Kinetics of the inversion, the dissociation of the spiro bonds and activation energy for torsions are discussed in detail. Compounds (Ia)-(Ic) do not undergo R⇔L inve… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
0
0

Publication Types

Select...

Relationship

0
0

Authors

Journals

citations
Cited by 0 publications
references
References 1 publication
0
0
0
Order By: Relevance

No citations

Set email alert for when this publication receives citations?