Highly Enantioselective Reduction of Prochiral Ketones with N,N-Diethylaniline • borane (DEANB) in Oxazaborolidine-Catalyzed Reductions. -A variety of prochiral ketones (I) is enantioselectively reduced to the corresponding alcohols (II) using diethylaniline borane in the presence of a chiral oxazab
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Highly enantioselective reduction of prochiral ketones with N,N-diethylaniline·borane (DEANB) in oxazaborolidine-catalyzed reductions
✍ Scribed by Ashok M. Salunkhe; Elizabeth R. Burkhardt
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 251 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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## Abstract The effect of borane source on enantioselectivity in the enantiopure oxazaborolidine‐catalyzed asymmetric borane reduction of ketones has been investigated by using (__S__)‐3,1,2‐oxazaborobicyclo[3.3.0]octane and (__S__)‐7,3,1,2‐thiaxazaborobicyclo[3.3.0]octane as catalysts. The results