2-fluoro- and 5-fluoro-3,4-dimethylphenethylamine derived from claisen rearrangement products

Michael T. Clark, Duane Miller

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

The Claisen rearrangement of 2-allyloxy-3-fluoroanisole followed by methylation provided the para-rearranged product along with the unexpected 3-(3,4-dimethoxy-2-fluorophenyl)-1-propene.

Original languageEnglish (US)
Pages (from-to)4299-4300
Number of pages2
JournalTetrahedron Letters
Volume26
Issue number36
DOIs
StatePublished - Jan 1 1985
Externally publishedYes

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Methylation
propylene
N,N-dimethylphenylethylamine

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

2-fluoro- and 5-fluoro-3,4-dimethylphenethylamine derived from claisen rearrangement products. / Clark, Michael T.; Miller, Duane.

In: Tetrahedron Letters, Vol. 26, No. 36, 01.01.1985, p. 4299-4300.

Research output: Contribution to journalArticle

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abstract = "The Claisen rearrangement of 2-allyloxy-3-fluoroanisole followed by methylation provided the para-rearranged product along with the unexpected 3-(3,4-dimethoxy-2-fluorophenyl)-1-propene.",
author = "Clark, {Michael T.} and Duane Miller",
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AU - Clark, Michael T.

AU - Miller, Duane

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N2 - The Claisen rearrangement of 2-allyloxy-3-fluoroanisole followed by methylation provided the para-rearranged product along with the unexpected 3-(3,4-dimethoxy-2-fluorophenyl)-1-propene.

AB - The Claisen rearrangement of 2-allyloxy-3-fluoroanisole followed by methylation provided the para-rearranged product along with the unexpected 3-(3,4-dimethoxy-2-fluorophenyl)-1-propene.

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