C. Shu

发表

Effects of catalyst activation and ligand steric properties on the enantioselective allylation of amines and phenoxides.

J. Hartwig, A. Leitner, C. Shu, 2005, Organic letters.

Editing the stereochemical elements in an iridium catalyst for enantioselective allylic amination.

J. Hartwig, A. Leitner, C. Shu, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Identification of an activated catalyst in the iridium-catalyzed allylic amination and etherification. Increased rates, scope, and selectivity.

C. Incarvito, J. Hartwig, C. Kiener, 2003, Journal of the American Chemical Society.

Enantioselective allylation of aromatic amines after in situ generation of an activated cyclometalated iridium catalyst.

J. Hartwig, A. Leitner, C. Shu, 2004, Angewandte Chemie.

A highly convergent and efficient synthesis of a macrocyclic hepatitis C virus protease inhibitor BI 201302.

C. Senanayake, Xudong Wei, N. Yee, 2013, Organic letters.

Adsorption of O2 on TiO2(110): A theoretical study

N. Sukumar, C. Ursenbach, C. Shu, 1999 .

Discovery of Imigliptin, a Novel Selective DPP-4 Inhibitor for the Treatment of Type 2 Diabetes.

Jun Xu, H. Ge, P. Peng, 2014, ACS medicinal chemistry letters.

Iridium-catalyzed intermolecular allylic etherification with aliphatic alkoxides: asymmetric synthesis of dihydropyrans and dihydrofurans.

J. Hartwig, C. Shu, 2004, Angewandte Chemie.

Enantiocontrolled synthesis of 2,3,6-trisubstituted piperidines using (eta(3)-dihydropyridinyl)molybdenum complexes as chiral scaffolds. Total synthesis of (-)-indolizidine 209B.

L. S. Liebeskind, A. Alcudia, J. Yin, 2001, Journal of the American Chemical Society.

Identification of an Activated Catalyst in the Iridium‐Catalyzed Allylic Amination and Etherification. Increased Rates, Scope, and Selectivity.

C. Incarvito, J. Hartwig, C. Kiener, 2004 .

Palladium-catalyzed cross-coupling of cyclopropylmagnesium bromide with aryl bromides mediated by zinc halide additives.

C. Senanayake, Xiaojun Wang, L. Zhang, 2010, The Journal of organic chemistry.

Second-Generation Process for the HCV Protease Inhibitor BILN 2061: A Greener Approach to Ru-Catalyzed Ring-Closing Metathesis†

Xudong Wei, Chris H. Senanayake, C. Senanayake, 2009 .

RCM macrocyclization made practical: an efficient synthesis of HCV protease inhibitor BILN 2061.

Xudong Wei, Ming-Hong Hao, M. Hao, 2008, Organic letters.

Simultaneous determination of imigliptin and its three metabolites in human plasma and urine by liquid chromatography coupled to tandem mass spectrometry.

Dongyang Liu, Hanlin Song, Yang Liu, 2015, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Solvolytic Studies of the Highly Deactivated 1‐Aryl‐1‐(trifluoromethyhethyl Tosylates.

C. Shu, M. Kuo, K.-T. Liu, 1982 .

Enantiocontrolled synthesis of 2,6-disubstituted piperidines by desymmetrization of meso-eta-(3,4,5)-dihydropyridinylmolybdenum complexes. application to the total synthesis of (-)-dihydropinidine and (-)-andrachcinidine.

L. S. Liebeskind, C. Shu, 2003, Journal of the American Chemical Society.

Simultaneous determination of imigliptin and its three metabolites in human plasma and urine by liquid chromatography coupled to tandem mass spectrometry.

Dongyang Liu, Hanlin Song, Yang Liu, 2015, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.