Pei-Qiang Huang focuses on Organic chemistry, Stereochemistry, Enantioselective synthesis, Alkylation and Amide. His study in Medicinal chemistry extends to Organic chemistry with its themes. His work deals with themes such as Coupling reaction, Umpolung and Alkyl, which intersect with Stereochemistry.
His Enantioselective synthesis research is multidisciplinary, incorporating elements of Samarium diiodide, Stereoisomerism, Pyrrolidine, Epimer and Carbanion. His Alkylation research incorporates themes from Lactam, Reagent and Aryl. The Amide study combines topics in areas such as Electrophile, Aldehyde, Organic synthesis, Combinatorial chemistry and Chemoselectivity.
His primary areas of study are Stereochemistry, Enantioselective synthesis, Organic chemistry, Total synthesis and Alkylation. His research in Stereochemistry intersects with topics in Ring and Stereoselectivity. His Enantioselective synthesis research is multidisciplinary, relying on both Regioselectivity, Synthon, Pyrrolidine, Alkyl and Combinatorial chemistry.
His research investigates the connection between Organic chemistry and topics such as Medicinal chemistry that intersect with issues in Pyrrole derivatives. He interconnects Yield, Stereocenter, Moiety, Aldehyde and Cascade reaction in the investigation of issues within Total synthesis. Basic research and Christian ministry are two areas of study in which Pei-Qiang Huang engages in interdisciplinary research.
Pei-Qiang Huang mainly focuses on Combinatorial chemistry, Catalysis, Organic chemistry, Enantioselective synthesis and Nucleophile. His studies deal with areas such as Vicinal, Trifluoromethanesulfonic anhydride, Cyanation and Organic synthesis as well as Combinatorial chemistry. Pei-Qiang Huang brings together Organic chemistry and Two step to produce work in his papers.
His Enantioselective synthesis study combines topics in areas such as Alcohol, Total synthesis, Stereochemistry and Stereoisomerism. Moiety is the focus of his Stereochemistry research. His Nucleophile research incorporates elements of Iminium, Amide and Chemoselectivity.
His scientific interests lie mostly in Combinatorial chemistry, Nucleophile, Chemoselectivity, Organic synthesis and Organic chemistry. His Combinatorial chemistry research includes themes of Ketyl and Catalysis, Enantioselective synthesis, Stereoisomerism. His research on Enantioselective synthesis focuses in particular on Enantiopure drug.
Pei-Qiang Huang has researched Nucleophile in several fields, including Acetaldehyde, Amide, Enol, Stereochemistry and Acylation. Pei-Qiang Huang combines subjects such as Ketone, Electrophile and Enol ether with his study of Chemoselectivity. His study in Total synthesis, Umpolung, Knoevenagel condensation, Aldehyde and Eschenmoser sulfide contraction is carried out as part of his Organic chemistry studies.
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Direct, one-pot sequential reductive alkylation of lactams/amides with Grignard and organolithium reagents through lactam/amide activation.
Kai-Jiong Xiao;Jie-Min Luo;Ke-Yin Ye;Yu Wang.
Angewandte Chemie (2010)
Orphan nuclear receptor TR3 acts in autophagic cell death via mitochondrial signaling pathway
Wei-jia Wang;Yuan Wang;Hang-zi Chen;Yong-zhen Xing.
Nature Chemical Biology (2014)
Asymmetric Synthesis of Hydroxylated Pyrrolidines, Piperidines and Related Bioactive Compounds: From N-Acyliminium Chemistry to N-α-Carbanion Chemistry
The orphan nuclear receptor Nur77 regulates LKB1 localization and activates AMPK
Yan-yan Zhan;Yan Chen;Qian Zhang;Jia-jia Zhuang.
Nature Chemical Biology (2012)
Direct Transformation of Secondary Amides into Secondary Amines: Triflic Anhydride Activated Reductive Alkylation†
Kai-Jiong Xiao;Ai-E Wang;Pei-Qiang Huang.
Angewandte Chemie (2012)
A Unique Pharmacophore for Activation of the Nuclear Orphan Receptor Nur77 In vivo and In vitro
Jing-jing Liu;Hui-ni Zeng;Lian-ru Zhang;Yan-yan Zhan.
Cancer Research (2010)
NSAID Sulindac and Its Analog Bind RXRα and Inhibit RXRα-Dependent AKT Signaling
Hu Zhou;Wen Liu;Ying Su;Zhen Wei.
Cancer Cell (2010)
Versatile One-Pot Reductive Alkylation of Lactams/Amides via Amide Activation: Application to the Concise Syntheses of Bioactive Alkaloids (+/-)-Bgugaine, (+/-)-Coniine, (+)-Preussin, and (-)-Cassine
Kai-Jiong Xiao;Yu Wang;Ke-Yin Ye;Pei-Qiang Huang.
Chemistry: A European Journal (2010)
Asymmetric Synthesis of (+)-L-733, 060 and (+)-CP-99, 994 Based on a New Chiral 3-Piperidinol Synthon†
Pei-Qiang Huang;Liang-Xian Liu;Bang-Guo Wei;Yuan-Ping Ruan.
Organic Letters (2003)
Impeding the interaction between Nur77 and p38 reduces LPS-induced inflammation
Li Li;Yuan Liu;Hang-zi Chen;Feng-wei Li.
Nature Chemical Biology (2015)
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