Oxazaborolidine-catalysed reduction of alk-2-ene-1,4-diones. A convenient access to chiral 1,4-diols
✍ Scribed by Jordi Bach; Ramon Berenguer; Jordi Garcia; Marta López; Judith Manzanal; Jaume Vilarrasa
- Book ID
- 108379134
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 908 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0040-4020
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📜 SIMILAR VOLUMES
A new synthetic route to C2-symmetric chiral 1,4-diols based on the borane-mediated oxazaborolidine-catalysed reduction of 2-ene-l,4-diones (2), of 2-yne-l,4-diones (3), and/or of Cocomplexed diketones 4 is described. Good to excellent enantio-and diastereoselectivities have been obtained in the red
A highly stereoselective and enantioselective reduction of racemic spiro[4.4]nonane-1,6-dione catalyzed by an oxazaborolidine reagent is described. The asymmetric reduction of the racemic spirodiketones resulted in enantiomerically pure spirodiols which are useful chiral auxiliaries and also key int