Issue 16, 1986
From the journal:

Journal of the Chemical Society, Chemical Communications

A photochemical synthesis of a thromboxane A2 analogue via intramolecular trapping of an oxacarbene by an hydroxy group

Stephen W. Jones,   Feodor Scheinmann,   Basil J. Wakefield,   David Middlemiss  and  Roger F. Newton  

Abstract

A spiro substituted 2,6-dioxabicyclo[3.1.1]heptane (the thromboxane A2 ring system) has been prepared by intramolecular trapping of a photochemically generated oxacarbene.

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Article information

DOI
https://doi.org/10.1039/C39860001260
Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 1260-1261

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A photochemical synthesis of a thromboxane A2 analogue via intramolecular trapping of an oxacarbene by an hydroxy group

S. W. Jones, F. Scheinmann, B. J. Wakefield, D. Middlemiss and R. F. Newton, J. Chem. Soc., Chem. Commun., 1986, 1260 DOI: 10.1039/C39860001260

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