Mary C. Walton

发表

Uncompetitive, adduct-forming SARM1 inhibitors are neuroprotective in preclinical models of nerve injury and disease

Sean P. Brown, C. Reynolds, P. R. B. Joseph, 2022, Neuron.

An intramolecular [2 + 2] cycloaddition of ketenimines via palladium-catalyzed rearrangements of N-allyl-ynamides.

R. Hsung, Wang Song, Mary C. Walton, 2012, Organic letters.

Stereoselective 6π-electron electrocyclic ring closures of 2-halo-amidotrienes via a remote 1,6-asymmetric induction.

R. Hsung, R. Hayashi, Xueliang Yu, 2010, Organic letters.

An efficient and practical entry to 2-amido-dienes and 3-amido-trienes from allenamides through stereoselective 1,3-hydrogen shifts

R. Hsung, R. Hayashi, Andrew G. Lohse, 2011, Beilstein journal of organic chemistry.

Synthesis of cyclopentenimines from N-allyl ynamides via a tandem aza-Claisen rearrangement-carbocyclization sequence.

R. Hsung, G. Winston-McPherson, Yu Zhang, 2013, The Journal of organic chemistry.

Discovery of a covalent inhibitor of KRASG12C (AMG 510) for the treatment of solid tumors.

N. Chen, J. McCarter, K. Rex, 2019, Journal of medicinal chemistry.

Ligand-Controlled Diastereoselective 1,3-Dipolar Cycloadditions of Azomethine Ylides with Methacrylonitrile.

L. Overman, K. Houk, Xin Hong, 2015, Organic letters.

Tricyclic analogues of epidithiodioxopiperazine alkaloids with promising in vitro and in vivo antitumor activity

L. Overman, M. Baumann, B. M. Loertscher, 2015, Chemical science.

Introducing a new class of N-phosphoryl ynamides via Cu(I)-catalyzed amidations of alkynyl bromides.

T. D. North, R. Hsung, Mary C. Walton, 2011, Organic letters.

Carbocyclization cascades of allyl ketenimines via aza-Claisen rearrangements of N-phosphoryl-N-allyl-ynamides.

R. Hsung, Mary C. Walton, Xiao-Na Wang, 2012, Organic letters.