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

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.

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Item Permalink: https://hdl.handle.net/21.11116/0000-0004-8C8B-2 Version Permalink: https://hdl.handle.net/21.11116/0000-0004-8C8C-1
Genre: Journal Article
Alternative Title : PROMOTED DIMERIZATION OF α-METHYLSTYRENE BY 3,5-DIMETHOXY-SUBSTITUENTS

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ChemistLett_9_1980_1005.pdf (Any fulltext), 4MB
 
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 Creators:
Schmitt, Bertram1, Author           
Birr, Christian1, Author           
Affiliations:
1Max Planck Institute for Medical Research, Max Planck Society, ou_1125545              

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 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.

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Language(s): eng - English
 Dates: 1980-06-092006-03-271980
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1246/cl.1980.1005
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Title: Chemistry Letters
  Other : Chem. Lett.
Source Genre: Journal
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Publ. Info: Tokyo : Chemical Society of Japan
Pages: - Volume / Issue: 9 (8) Sequence Number: - Start / End Page: 1005 - 1008 Identifier: ISSN: 0366-7022
CoNE: https://pure.mpg.de/cone/journals/resource/954925524760