Pei-Qiang Huang
0000-0003-3230-0457
Université Paris-Sud
188 papers found
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Low-Valent Titanium-Mediated Enantioselective Synthesis of Quinazolinone Alkaloids Circumdatins F, H, and Analogs
Procedure—economical enantioselective total syntheses of asperlicins C and E
A General Method for the One-Pot Reductive Functionalization of Secondary Amides
General and Chemoselective Bisphosphonylation of Secondary and Tertiary Amides
The first enantioselective total synthesis of (+)-preussin B and an improved synthesis of (+)-preussin by step-economical methods
Simple, versatile, and chemoselective reduction of secondary amides and lactams to amines with the Tf 2 O–NaBH 4 or Cp 2 ZrHCl–NaBH 4 system
Direct transformation of amides: a one-pot reductive Ugi-type three-component reaction of secondary amides
Aza-Knoevenagel-type condensation of secondary amides: direct access to N-monosubstituted β,β-difunctionalized enamines
Enantioselective Total Synthesis of (+)-Methoxystemofoline and (+)-Isomethoxystemofoline
Direct reductive coupling of secondary amides: chemoselective formation of vicinal diamines and vicinal amino alcohols
SmI2-Mediated Radical Coupling Strategy to Securinega Alkaloids: Total Synthesis of (−)-14,15-Dihydrosecurinine and Formal Total Synthesis of (−)-Securinine
Towards Reaction Control: An Expeditious Access to Racemic 5-Substituted Tetramates and 5-Substituted Tetramic Acids from Malimides
Bio-inspired Step-Economical, Redox-Economical and Protecting-Group-Free Enantioselective Total Syntheses of (−)-Chaetominine and Analogues
Tertiary amide-based Knoevenagel-type reactions: a direct, general, and chemoselective approach to enaminones
Sulindac-Derived RXRα Modulators Inhibit Cancer Cell Growth by Binding to a Novel Site
A concise formal stereoselective total synthesis of (−)-swainsonine
Efficient asymmetric syntheses of alkaloids and medicinally relevant molecules based on heterocyclic chiral building blocks
Progress of organic chemistry (2011~2012)
Complexity generation by chemical synthesis: a five-step synthesis of (-)-chaetominine from L-tryptophan and its biosynthetic implications
A versatile two-step method for the reductive alkylation and formal [4 + 2] annulation of secondary lactams: step economical syntheses of the ant venom alkaloids (2R,5S)-2-butyl-5-propylpyrrolidine and (+)-monomorine I
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