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Reduction of Ketones using Secondary Alcohol Reductant under Mildly Basic Conditions published in Organic Letters

An electron-rich benzylic secondary alcohol enables the reduction of a wide range of aromatic ketones under mildly basic conditions without the need for a transition or main group metal catalysts, with the potential for synthesis of enantioenriched products!

Publication 110.

Research NewsJulio GonzalezJuly 31, 20192019
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A Perspective on Recent Collaborations in Total Synthesis

Research NewsJulio GonzalezAugust 5, 20192019
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An undergraduate organic chemistry laboratory experiment utilizing paraffin-encapsulated Nickel catalysts for amide esterification published in J. Chem. Educ.

Research NewsJulio GonzalezJuly 31, 20192019
  2025 Neil Garg
  neilgarg@chem.ucla.edu
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