Xuanjia Peng

发表

Selections and Screenings of DNA-Encoded Chemical Libraries against Enzyme and Cellular Targets.

A. Satz, Letian Kuai, Xuanjia Peng, 2021, Bioorganic & medicinal chemistry letters.

DNA Compatible Intermolecular Wittig Olefination for the Construction of α, β-Unsaturated Carbonyl Compounds.

Shien Liu, Yulong An, Wenji Su, 2020, Organic letters.

Copper-Mediated DNA-Compatible One-Pot Click Reactions of Alkynes with Aryl Borates and TMS-N3.

Rui Ge, A. Satz, Wenji Su, 2020, Organic letters.

Synthesis of 1,2-Amino Alcohols by Photoredox-Mediated Decarboxylative Coupling of α-Amino Acids and DNA-Conjugated Carbonyls.

Rui Ge, A. Satz, Yulong An, 2020, Organic letters.

Design, synthesis, and biological evaluation of anti-EV71 agents.

Z. Gu, Zhenzhong Wang, Peng Li, 2016, Bioorganic & medicinal chemistry letters.

Development of a New Structural Class of Broadly Acting HCV Non‐Nucleoside Inhibitors Leading to the Discovery of MK‐8876

A. Palani, M. Holloway, N. Liverton, 2017, ChemMedChem.

A general approach to access 5,6-dihydroindolo-naphthyridine ring system

Q. Dang, A. Palani, Peng Li, 2017 .

Fragment-wise design of inhibitors to 3C proteinase from enterovirus 71.

Peng Li, Tianwei Lin, Y. Guan, 2016, Biochimica et biophysica acta.

A general approach to substituted 6H-pyrido[2′,3′:5,6] [1,3]oxazino[3,4-a]indole via cyclization from an indoline precursor followed by re-aromatization

Q. Dang, A. Palani, P. Li, 2013 .

Palladium-mediated Suzuki-Miyaura Cross-Coupling Reaction of Potassium Boc-protected aminomethyltrifluoroborate with DNA-Conjugated aryl bromides for DNA-Encoded chemical library synthesis.

A. Satz, Yulong An, Wenji Su, 2020, Biochemical and biophysical research communications.

First Asymmetric Total Synthesis of Mansonone P and R

Xuanjia Peng, X. She, Xin-fu Pan, 2004 .

A Strategy for the Synthesis of Sulfonamides on DNA.

Justin D Dietrich, Xuanjia Peng, Hongfang Yang, 2019, Organic letters.

Conformational Plasticity of the 2A Proteinase from Enterovirus 71

Yaozong Li, Tianwei Lin, M. Yameen, 2013, Journal of Virology.

Discovery of selective, orally bioavailable, N-linked arylsulfonamide Nav1.7 inhibitors with pain efficacy in mice.

Edward C Sherer, John Majercak, Deping Wang, 2017, Bioorganic & medicinal chemistry letters.

Total Synthesis of (±)-Abieta-8,11,13-trien-7β-ol

Xuanjia Peng, Xin-fu Pan, Chenglu Zhang, 2003 .

First Total Synthesis of (±)‐Celaphanol A

Xuanjia Peng, Tongxing Wu, Xin-fu Pan, 2002 .

Hydroxy tricyclic 1,5-naphthyridinone oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents-SAR of RHS moiety (Part-3).

R. Nargund, Akinori Nishimura, Jin Wu, 2015, Bioorganic & medicinal chemistry letters.

Tricyclic 1,5-naphthyridinone oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents-SAR of left-hand-side moiety (Part-2).

Leo A. Joyce, E. Sherer, R. Nargund, 2015, Bioorganic & medicinal chemistry letters.

C1–C2-linker substituted 1,5-naphthyridine analogues of oxabicyclooctane-linked NBTIs as broad-spectrum antibacterial agents (part 7)

Akinori Nishimura, Jin Wu, Xuanjia Peng, 2015 .

Structure activity relationship of pyridoxazinone substituted RHS analogs of oxabicyclooctane-linked 1,5-naphthyridinyl novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-6).

Akinori Nishimura, Jin Wu, Xuanjia Peng, 2015, Bioorganic & medicinal chemistry letters.

Structures of Enterovirus 71 3C proteinase (strain E2004104-TW-CDC) and its complex with rupintrivir.

Xiaolong Wang, Tianwei Lin, Xuanjia Peng, 2013, Acta crystallographica. Section D, Biological crystallography.

Solution-Phase DNA-Compatible Pictet-Spengler Reaction Aided by Machine Learning Building Block Filtering

Ke Li, Kaixian Chen, Mingyue Zheng, 2020, iScience.

The first total synthesis of (R)-7-butyl-6,8-dihydroxy-3-pentylisochroman-1-one

Xuanjia Peng, Tongxing Wu, Jun-Wei Ma, 2005 .

Hydroxy tricyclic 1,5-naphthyridinone oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents-SAR of RHS moiety (Part-3).

R. Nargund, Akinori Nishimura, Jin Wu, 2015, Bioorganic & medicinal chemistry letters.