Issue 20, 1970
From the journal:

Journal of the Chemical Society D: Chemical Communications

An unusual stereoelectronic effect in the rearrangement of the Diels–Alder adducts of cyclopropene and furan

Ronald W. LaRochelle  and  Barry M. Trost  

Abstract

Cyclopropene formed the exo and endo Diels–Alder adducts in a 1 : 1 ratio with furan; only the endo-isomer readily rearranges to cycloheptadienones.

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Article information

DOI
https://doi.org/10.1039/C29700001353
Article type
Paper

J. Chem. Soc. D, 1970, 1353-1354

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An unusual stereoelectronic effect in the rearrangement of the Diels–Alder adducts of cyclopropene and furan

R. W. LaRochelle and B. M. Trost, J. Chem. Soc. D, 1970, 1353 DOI: 10.1039/C29700001353

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