Novel spiroborate esters derived nonracemic 1,2-aminoalcohols and ethylene glycol are reported as highly effective catalysts for the asymmetric borane reduction of a variety of prochiral ketones with borane-dimethyl sulfide complex at room temperature. Optically active alcohols were obtained in excellent chemical yields using 0.1 to 10 mol % of catalysts with up to 99% ee.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2701200PMC
http://dx.doi.org/10.1016/j.tetlet.2007.06.086DOI Listing

Publication Analysis

Top Keywords

prochiral ketones
8
spiroborate esters
8
enantioselective reduction
4
reduction prochiral
4
ketones spiroborate
4
esters catalysts
4
catalysts novel
4
novel spiroborate
4
esters derived
4
derived nonracemic
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!