A Highly Stereoselective Synthesis of (E,E)-1,5-Dienes
Publication Type
Original research
Authors
  • Mohammed Al-Nuri
  • Joseph J Tufariello
  • Arnold S Milowsky
  • Steven Goldstein

Several representative 1,5-dienes were synthesized, with a high degree of regioselectivity, by a series of nitrone cycloadditions and subsequent deamination of the adducts.

Amines of the type View the MathML source, readily available by the utilization of nitrone cycloaddition chemistry, were deazetized via the corresponding diazenes to afford 1,5-dienes with a high degree of stereochemical control.

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Journal
Title
Tetrahedron Letters Volume 28, Issue 3, Pages 263–266
Publisher
--
Publisher Country
Palestine
Publication Type
Both (Printed and Online)
Volume
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Year
1987
Pages
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