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  Pericyclic reactions in nature: Synthesis and cope rearrangement of thermolabile bis-alkenylcyclopropanes from female gametes of marine brown algae (Phaeophyceae)

Pohnert, G., & Boland, W. (1997). Pericyclic reactions in nature: Synthesis and cope rearrangement of thermolabile bis-alkenylcyclopropanes from female gametes of marine brown algae (Phaeophyceae). Tetrahedron, 53(40), 13681-13694. doi:10.1016/S0040-4020(97)00886-7.

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Pohnert, G.1, Author           
Boland, Wilhelm1, Author           
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1Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society, ou_24028              

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Free keywords: Desmarestia-aculeata; cutleria-multifida; sexual pheromones; biosynthesis; hydrocarbons; receptor
 Abstract: The biosyntheses of the 6-substituted cyclohepta-1,4-dienes dictyotene (1), ectocarpene (2), desmarestene (3), vinylcycloheptadiene (4) and lamoxirene (5) involve a spontaneous Cope rearrangement of thermolabile bis- alkenylcyclopropane precursors like

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 Dates: 1997
 Publication Status: Published in print
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 Identifiers: Other: BOL041
DOI: 10.1016/S0040-4020(97)00886-7
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Title: Tetrahedron
  Other : Tetrahedron
Source Genre: Journal
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Publ. Info: Oxford : Pergamon
Pages: - Volume / Issue: 53 (40) Sequence Number: - Start / End Page: 13681 - 13694 Identifier: ISSN: 0040-4020
CoNE: https://pure.mpg.de/cone/journals/resource/954925448773