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 H.J. Cordes; Susan de Gala; Jerome A. Berson

doi:10.1021/ja00103a043

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 H.J. Cordes, Susan de Gala, Jerome A. Berson

Research output: Contribution to journal › Article › peer-review

Original language	English (US)
Pages (from-to)	11161-11162
Number of pages	2
Journal	Journal of the American Chemical Society
Volume	116
Issue number	24
DOIs	https://doi.org/10.1021/ja00103a043
State	Published - Nov 1 1994
Externally published	Yes

ASJC Scopus subject areas

Catalysis
General Chemistry
Biochemistry
Colloid and Surface Chemistry

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10.1021/ja00103a043

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Cordes, M. H. J., de Gala, S., & Berson, J. A. (1994). 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. Journal of the American Chemical Society, 116(24), 11161-11162. https://doi.org/10.1021/ja00103a043

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. / Cordes, Matthew H.J.; de Gala, Susan; Berson, Jerome A.
In: Journal of the American Chemical Society, Vol. 116, No. 24, 01.11.1994, p. 11161-11162.

Research output: Contribution to journal › Article › peer-review

Cordes, MHJ, de Gala, S & Berson, JA 1994, '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', Journal of the American Chemical Society, vol. 116, no. 24, pp. 11161-11162. https://doi.org/10.1021/ja00103a043

Cordes MHJ, de Gala S, Berson JA. 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. Journal of the American Chemical Society. 1994 Nov 1;116(24):11161-11162. doi: 10.1021/ja00103a043

Cordes, Matthew H.J. ; de Gala, Susan ; Berson, Jerome A. / 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. In: Journal of the American Chemical Society. 1994 ; Vol. 116, No. 24. pp. 11161-11162.

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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

ASJC Scopus subject areas

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