Abstract
The preparation and application of a new reagent for stereoselective deuterium addition to substituted cyclohexanones is described affording cyclohexanols with axial hydroxy group with high stereoselectivity. The results are compared with other established reduction methods.
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APA
Gärtner, P., Novak, C., Knollmüller, M., & Gmeiner, G. (2001). Lithium tri-sec-butylborodeuteride: A new reagent for the stereoselective deuterium addition to cyclohexanones with single chair conformations. Arkivoc, 2001(2), 9–20. https://doi.org/10.3998/ark.5550190.0002.202
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