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Catalytic and Stoichiometric Enantioselective Addition of Diethylzinc to Aldehydes Using a Novel Chiral Spirotitanate

✍ Scribed by Dipl.-Chem. Beat Schmidt; Prof. Dr. Dieter Seebach


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
364 KB
Volume
30
Category
Article
ISSN
0044-8249

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✦ Synopsis


main product 19, ca. 20% of another stereoisomer. This results from a partial racemization of the ketone 5 occurring during its distillation or during the formation of 18. This follows from the condensation of racemic 5 with the aldehyde 15 affording with a 4: 1 selectivity the above mentioned by-product, which must therefore be 12-epi-19.


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