James Lalonde

Lipase-catalyzed irreversible transesterifications using enol esters as acylating reagents: preparative enantio- and regioselective syntheses of alcohols, glycerol derivatives, sugars and organometallics

Yi Fong. Wang, James Lalonde, M. Momongan et al. · Journal of the American Chemical Society · 1988 · 530 citations

Enol Esters, Bioorganic Chemistry, Glycerol Derivatives +14

Development of a Biocatalytic Process as an Alternative to the (−)-DIP-Cl-Mediated Asymmetric Reduction of a Key Intermediate of Montelukast

Jack Liang, James Lalonde, Birthe Borup et al. · Organic Process Research & Development · 2009 · 223 citations

Key Intermediate, Engineering, Asymmetric Reduction +19

Efficient, Chemoenzymatic Process for Manufacture of the Boceprevir Bicyclic [3.1.0]Proline Intermediate Based on Amine Oxidase-Catalyzed Desymmetrization

Tao Li, Jack Liang, Alexandre Ambrogelly et al. · Journal of the American Chemical Society · 2012 · 210 citations

Bioorganic Chemistry, New Drug Treatment, Organic Chemistry +21

Directed evolution of an ultrastable carbonic anhydrase for highly efficient carbon capture from flue gas

Oscar Alvizo, Luan J. Nguyen, Christopher K. Savile et al. · Proceedings of the National Academy of Sciences · 2014 · 190 citations · Full text

Cross-Linked Crystals of Candida rugosa Lipase: Highly Efficient Catalysts for the Resolution of Chiral Esters

James Lalonde, Chandrika P. Govardhan, Nazer Khalaf et al. · Journal of the American Chemical Society · 1995 · 168 citations

Engineering, Altmetric Attention Score, Organic Chemistry +17