Ai-E Wang

发表

Design and Synthesis of Camphor-derived Chiral [1,2,4]Triazolo[4,3-a]tetrahydroquinoline N-Heterocyclic Carbene Precursors by Pd-Catalyzed Coupling Reactions of Aryl Hydrazides with a Pyridyl Triflate Derivative

Pei‐Qiang Huang, Minglian Lin, Liang-An Chen, 2013 .

Enantioselective total synthesis of (+)-methoxystemofoline and (+)-isomethoxystemofoline.

Pei‐Qiang Huang, Zhongyi Mao, Su-Yu Huang, 2015, Chemical communications.

Chiral imidazo[1,5-a]tetrahydroquinoline N-heterocyclic carbenes and their copper complexes for asymmetric catalysis

Pei‐Qiang Huang, Yuanping Ruan, Ruirui Xu, 2013 .

SmI2-mediated radical coupling strategy to Securinega alkaloids: total synthesis of (-)-14,15-dihydrosecurinine and formal total synthesis of (-)-securinine.

Juan Liu, Pei‐Qiang Huang, Chen-Xi Ye, 2015, The Journal of organic chemistry.

A concise formal stereoselective total synthesis of (−)-swainsonine

Pei‐Qiang Huang, Ai-E Wang, Xiao-Gang Wang, 2014 .

Tf2 O-Mediated Intermolecular Coupling of Secondary Amides with Enamines or Ketones: A Versatile and Direct Access to β-Enaminones

Pei‐Qiang Huang, Ai-E Wang, Yong-peng Liu, 2019, European Journal of Organic Chemistry.

Enamines as Surrogates of Alkyl Carbanions for the Direct Conversion of Secondary Amides to α-Branched Ketones

Pei‐Qiang Huang, Shu-Ren Wang, Ting-Ting Chen, 2019, Advanced Synthesis & Catalysis.

A novel and versatile method for the enantioselective syntheses of tropane alkaloids

Pei‐Qiang Huang, Zhongyi Mao, Su-Yu Huang, 2014, Science China Chemistry.

Concise asymmetric total synthesis of 9-epi-sessilifoliamide J.

Jian-Liang Ye, Pei‐Qiang Huang, Su-Yu Huang, 2011, Organic letters.

Reductive hydroxyalkylation/alkylation of amines with lactones/esters.

Jian-Liang Ye, Pei‐Qiang Huang, Yu-huang Wang, 2012, Organic & biomolecular chemistry.

Titanocene(III)-Catalyzed Three-Component Reaction of Secondary Amides, Aldehydes, and Electrophilic Alkenes.

Pei‐Qiang Huang, Xi-Jie Dai, Xiao Zheng, 2015, Angewandte Chemie.

General and chemoselective bisphosphonylation of secondary and tertiary amides.

Pei‐Qiang Huang, Zong Chang, Ai-E Wang, 2015, Organic letters.

Tertiary amide-based Knoevenagel-type reactions: a direct, general, and chemoselective approach to enaminones.

W. Ou, Pei‐Qiang Huang, Kai-Jiong Xiao, 2014, Chemical communications.

Complexity generation by chemical synthesis: a five-step synthesis of (-)-chaetominine from L-tryptophan and its biosynthetic implications.

Pei‐Qiang Huang, Shi‐Peng Luo, Chunyan Xu, 2014, Organic & biomolecular chemistry.

Direct transformation of secondary amides into secondary amines: triflic anhydride activated reductive alkylation.

Pei‐Qiang Huang, Kai-Jiong Xiao, Ai‐E Wang, 2012, Angewandte Chemie.

Bio-inspired Step-Economical, Redox-Economical and Protecting-Group-Free Enantioselective Total Syntheses of (−)-Chaetominine and Analogues

Pei‐Qiang Huang, Shi‐Peng Luo, Chunyan Xu, 2014 .

Procedure—economical enantioselective total syntheses of asperlicins C and E

Pei‐Qiang Huang, Yuanping Ruan, Yu Wang, 2015 .

Enantioselective syntheses of rigidiusculamides A and B: revision of the relative stereochemistry of rigidiusculamide A.

Hui-Ying Huang, Hong-kui Zhang, Jian-Liang Ye, 2012, Chemistry, an Asian journal.

A flexible asymmetric approach to methyl 5-alkyltetramates and its application in the synthesis of cytotoxic marine natural product belamide A.

Jian-Liang Ye, Pei‐Qiang Huang, Yuanping Ruan, 2011, Chemistry.

A new approach to the C28 fatty acid chain of the marine natural products schulzeines B and C: a concise diastereoselective total synthesis of(−)-schulzeine B

Jian-Liang Ye, Pei‐Qiang Huang, Chao Yang, 2011 .

Mild N-deacylation of secondary amides by alkylation with organocerium reagents

Pei‐Qiang Huang, Zong Chang, Ai-E Wang, 2015 .

Direct reductive coupling of secondary amides: chemoselective formation of vicinal diamines and vicinal amino alcohols.

Pei‐Qiang Huang, Jian-Feng Zheng, Qiwei Lang, 2015, Chemical communications.

Chemoselective Synthesis of α-Amino-α-cyanophosphonates by Reductive Gem-Cyanation-Phosphonylation of Secondary Amides.

Pei‐Qiang Huang, Ting-Ting Chen, Ai-E Wang, 2019, Organic letters.

Versatile and Direct Transformation of Secondary Amides into Ketones by Deaminative Alkylation with Organocerium Reagents

Pei‐Qiang Huang, Kai-Jiong Xiao, Ying-Hong Huang, 2012 .

Modular enantioselective synthesis of 8-aza-prostaglandin E1.

Pei‐Qiang Huang, Yuanping Ruan, Ai-E Wang, 2013, The Journal of organic chemistry.

Progress on the total synthesis of natural products in China: From 2006 to 2010

Pei‐Qiang Huang, Jie Chen, Haohua Huo, 2012, Science China Chemistry.

Efficient asymmetric syntheses of alkaloids and medicinally relevant molecules based on heterocyclic chiral building blocks

Pei‐Qiang Huang, Ai-E Wang, 2014 .

Enantioselective Reductive Cyanation and Phosphonylation of Secondary Amides by Ir and Chiral Thiourea Sequential Catalysis.

Pei‐Qiang Huang, Dong‐Ping Wu, Dong‐Huang Chen, 2021, Angewandte Chemie.

Enamines as Surrogates of Alkene Carbanions for the Reductive Alkenylation of Secondary Amides: An Approach to Allylamines.

Pei‐Qiang Huang, Ting-Ting Chen, Ai-E Wang, 2018, Organic letters.

Versatile construction of functionalized tropane ring systems based on lactam activation: enantioselective synthesis of (+)-pervilleine B.

Pei‐Qiang Huang, Su-Yu Huang, Long-Hui Gao, 2013, Chemical communications.

Direct reductive coupling of secondary amides: chemoselective formation of vicinal diamines and vicinal amino alcohols.

Pei‐Qiang Huang, Jian-Feng Zheng, Qiwei Lang, 2015, Chemical communications.