C. Vo

发表

Exploring Aurone Derivatives as Potential Human Pancreatic Lipase Inhibitors through Molecular Docking and Molecular Dynamics Simulations

T. Tran, P. Nguyen, H. Huynh, 2020, Molecules.

SnAP reagents for the synthesis of piperazines and morpholines.

J. Bode, C. Vo, Michael U. Luescher, 2014, Organic letters.

SnAP reagents for the one-step synthesis of medium-ring saturated N-heterocycles from aldehydes.

J. Bode, C. Vo, Michael U. Luescher, 2014, Nature chemistry.

SnAP reagents for the one-step synthesis of medium-ring saturated N-heterocycles from aldehydes.

J. Bode, C. Vo, Michael U. Luescher, 2014, Nature chemistry.

Exploration of chalcones as 3-chymotrypsin-like protease (3CLpro) inhibitors of SARS-CoV-2 using computational approaches

K. Thai, T. Tran, M. Le, 2022, Structural Chemistry.

Expanded substrate scope and improved reactivity of ether-forming cross-coupling reactions of organotrifluoroborates and acetals.

J. Bode, C. Vo, T. Mitchell, 2011, Journal of the American Chemical Society.

Exploration of chalcones as 3-chymotrypsin-like protease (3CLpro) inhibitors of SARS-CoV-2 using computational approaches

K. Thai, T. Tran, M. Le, 2022, Structural Chemistry.

New cross-coupling strategies for the synthesis of dialkyl ethers and saturated N-heterocycles

C. Vo, 2014 .

Synthesis of saturated N-heterocycles.

J. Bode, C. Vo, 2014, The Journal of organic chemistry.

SnAP reagents for the transformation of aldehydes into substituted thiomorpholines--an alternative to cross-coupling with saturated heterocycles.

J. Bode, Gediminas Mikutis, C. Vo, 2013, Angewandte Chemie.

Discovery of novel flavonoid derivatives as potential dual inhibitors against α-glucosidase and α-amylase: virtual screening, synthesis, and biological evaluation.

K. Thai, T. Tran, Tan Thanh Mai, 2023, Molecular diversity.

Computational assessment and in vitro test of phytochemicals of Usnea aciculifera as potential inhibitors of Escherichia coli efflux pump AcrB.

K. Thai, T. Tran, M. Le, 2023, Journal of biomolecular structure & dynamics.