English
 
User Manual Privacy Policy Disclaimer Contact us
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Promoted dimerization of α-methylstyrene by 3,5-dimethoxy-substituents

MPS-Authors
/persons/resource/persons211525

Schmitt,  Bertram
Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons206231

Birr,  Christian
Max Planck Institute for Medical Research, Max Planck Society;

Fulltext (public)
There are no public fulltexts available
Supplementary Material (public)
There is no public supplementary material available
Citation

Schmitt, B., & Birr, C. (1980). Promoted dimerization of α-methylstyrene by 3,5-dimethoxy-substituents. Chemistry Letters, 9(8), 1005-1008. doi:10.1246/cl.1980.1005.


Cite as: http://hdl.handle.net/21.11116/0000-0004-8C8B-2
Abstract
3,5-Dimethoxy-α-methylstyrene, which originates from acidic cleavage of the 3,5-dimethoxy-α,α-dimethyl-benzyl-oxycarbonyl residue, an amino protecting group in peptide synthesis, easily dimerizes in solution to 1,3,3-trimethyl-1-(3,5-dimethoxy)-phenyl-5,7-dimethoxyindan in the presence of trifluoroacetic aciEd.