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Skeletal rearrangement of 6,8-dioxabicyclo[3.2.1]octan-4-ols promoted by thionyl chloride or Appel conditions

A skeletal rearrangement of a series of 6,8-dioxabicyclo[3.2.1]octan-4-ols has been developed using SOCl2 in the presence of pyridine. An oxygen migration from C5 to C4 was observed when the C4 alcohols were treated with SOCl2/pyridine, giving a 2-chloro-3,8-dioxabicyclo[3.2.1]octane ring-system via...

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I tiakina i:
Ngā taipitopito rārangi puna kōrero
Ngā kaituhi matua: Martyn Jevric, Julian Klepp, Johannes Puschnig, Oscar Lamb, Christopher J. Sumby, Ben W. Greatrex
Hōputu: Artigo
Reo:Inglês
I whakaputaina: Beilstein-Institut 2024-04-01
Rangatū:Beilstein Journal of Organic Chemistry
Ngā marau:
Urunga tuihono:https://doi.org/10.3762/bjoc.20.74
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