Catalytic and Stoichiometric Enantioselective Addition of Diethylzinc to Aldehydes Using a Novel Chiral Spirotitanate
β 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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β¦ 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.
π SIMILAR VOLUMES
The asymmetric alkylation with diethylzinc of five heterocyclic aldehydes and benzaldehyde (for comparison) has been studied in the presence of two optically active amino alcohols: (S)-2-amino-1-butanol (AB) and (1S,2R)-N,Ndibutylnorephedrine (DBNE). A number of chiral (hetero)aromatic secondary alc
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