Stereochemistry of a cyclopropanone by crystal structure analysis. The exo configuration of the diels-alder adduct of cyclopropenone and 1,3-diphenylisobenzofuran appears to be stabilized relative to the endo by an attractive ether-carbonyl interaction

Matthew Hj Cordes, Susan De Gala, Jerome A. Berson

Research output: Contribution to journalArticle

23 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)11161-11162
Number of pages2
JournalJournal of the American Chemical Society
Volume116
Issue number24
StatePublished - Nov 30 1994
Externally publishedYes

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Stereochemistry
Ether
Ethers
Crystal structure
cyclopropenone
1,3-diphenylisobenzofuran

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

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title = "Stereochemistry of a cyclopropanone by crystal structure analysis. The exo configuration of the diels-alder adduct of cyclopropenone and 1,3-diphenylisobenzofuran appears to be stabilized relative to the endo by an attractive ether-carbonyl interaction",
author = "Cordes, {Matthew Hj} and {De Gala}, Susan and Berson, {Jerome A.}",
year = "1994",
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AU - De Gala, Susan

AU - Berson, Jerome A.

PY - 1994/11/30

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