Volume 27, Issue 13
Physical Organic Chemistry
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ChemInform Abstract: endo-5-Methyl-exo-6-phenylseleno-endo-tricyclo(5.2.1.02,6)dec-8-en-3- one.

F. G. MOERS

F. G. MOERS

Crystallogr. Lab., Univ. Nijmegen, NL-6525 ED Nijmegen, Neth.

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J. M. M. SMITS

J. M. M. SMITS

Crystallogr. Lab., Univ. Nijmegen, NL-6525 ED Nijmegen, Neth.

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P. T. BEURSKENS

P. T. BEURSKENS

Crystallogr. Lab., Univ. Nijmegen, NL-6525 ED Nijmegen, Neth.

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J. ZHU

J. ZHU

Crystallogr. Lab., Univ. Nijmegen, NL-6525 ED Nijmegen, Neth.

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A. J. H. KLUNDER

A. J. H. KLUNDER

Crystallogr. Lab., Univ. Nijmegen, NL-6525 ED Nijmegen, Neth.

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First published: March 26, 1996

Abstract

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ChemInform Abstract

The 6-phenylselenyl group completely controls the stereochemistry of the conjugate dimethyllithiumcuprate addition to the endo- tricyclodecadienone (I) to give title compound (III) in nearly quantitative yield as single addition product. The endo configuration of the C-5 methyl group is confirmed by X-ray diffraction analysis.

chemical structure image

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