3336-61-6Relevant academic research and scientific papers
Acylotropic tautomerism: XXXV. R?L-inversion of configuration of dipolar spyrocyclic and open-chain 2-arylaminotropone isomers
Olekhnovich,Budarina,Borodkin,Kurbatov,Vaslyaeva,Zhdanov
, p. 713 - 722 (2007/10/03)
R?L-Inversion of chiral spirocyclic and open-chain 2-arylaminotropone derivatives with varied heteroatom (O, S, N) has been studied. Kinetic relations holding in the R,L-permutation are discussed. Its mechanism includes formation and dissociation of spiro bonds and torsion stereodynamics.
