Ning Shao, Ph.D.

Affiliations: 
2005 Case Western Reserve University, Cleveland Heights, OH, United States 
Area:
Pharmaceutical Chemistry, Organic Chemistry
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"Ning Shao"
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Parents

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Zhongwu Guo grad student 2005 Case Western
 (Synthetic studies of glycopeptides and glycoconjugates.)
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Publications

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Wu Y, Chen K, Wu X, et al. (2021) Superfast and Water-Insensitive Polymerization on α-Amino Acid N-Carboxyanhydrides to Prepare Polypeptides using Tetraalkylammonium carboxylates as the Initiator. Angewandte Chemie (International Ed. in English)
Xiao D, Zhu X, Sofolarides M, et al. (2014) Discovery of a novel series of potent MK2 non-ATP competitive inhibitors using 1,2-substituted azoles as cis-amide isosteres. Bioorganic & Medicinal Chemistry Letters. 24: 3609-13
Shao N, Aslanian R, West RE, et al. (2012) Synthesis and structure-activity relationship (SAR) study of 4-azabenzoxazole analogues as H3 antagonists. Bioorganic & Medicinal Chemistry Letters. 22: 2075-8
Shao N, Huang X, Palani A, et al. (2010) ChemInform Abstract: New Applications of PhI(OAc)2in Synthesis: Total Synthesis and SAR Development of Potent Antitumor Natural Product Psymberin/Irciniastatin A. Cheminform. 41
Huang X, Shao N, Huryk R, et al. (2009) The discovery of potent antitumor agent C11-deoxypsymberin/irciniastatin A: total synthesis and biology of advanced psymberin analogs. Organic Letters. 11: 867-70
Shao N, Huang X, Palani A, et al. (2009) New Applications of PhI(OAc)2 in Synthesis: Total Synthesis and SAR Development of Potent Antitumor Natural Product Psymberin/Irciniastatin A Synthesis. 2009: 2855-2872
Huang X, Shao N, Palani A, et al. (2008) Synthesis of seco-psymberin/irciniastatin A: the discovery of a novel PhI(OAc)2 mediated cascade cyclization reaction Tetrahedron Letters. 49: 3592-3595
Huang X, Shao N, Palani A, et al. (2007) The total synthesis of psymberin. Organic Letters. 9: 2597-600
Huang X, Shao N, Palani A, et al. (2007) Synthesis of Psymberin Synfacts. 2007: 1126-1126
Huang X, Shao N, Palani A, et al. (2007) Oxidative Entry to α-Oxy N-Acyl Aminals and Hemiaminals: Efficient Formation of 2-(N-Acylaminal) Substituted Tetrahydropyrans. Cheminform. 38
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