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First and Highly Diastereoselective Synthesis of Palladepanes
Authors:Hashmi   Rivas Nass A   Bats   Bolte
Affiliation:Institut für Organische Chemie der Universit?t, Marie-Curie-Strasse 11, D-60439 Frankfurt (Germany).
Abstract:Unexpected stability is observed for the palladacycloheptane rac-2, which is obtained as major product and single diastereomer from the cyclization of 1 and Pd(0). Up to a temperature of 50 degrees C 2 shows neither reductive elimination nor intramolecular insertion of another olefin.
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