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Improvement of the diastereoselectivity of the cobalt-mediated [2+2+2] cycloaddition of substituted linear enediynes

โœ Scribed by Franck Slowinski; Corinne Aubert; Max Malacria


Book ID
108387295
Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
212 KB
Volume
40
Category
Article
ISSN
0040-4039

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Improvement of the Diastereoselectivity of the Cobalt-Mediated [2 + 2 + 2] Cycloaddition of Substituted Linear Enediynes. -Substituting the terminal triple bond or the double bond in the enediynes (I) with ester, phosphine oxide or sulfoxide groups improves the level of diastereoselectivity in the

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The cobalt(I)-catalyzed highly stereoselective [2+2+2] cyclization has been realized for the first time with chiral phosphine oxides substituted linear enediynes. Depending the substituents on the phosphorus atom, the cycloaddition was achieved with a level of diastereoseleetivity of 74%.