What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Enzyme
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 most cited work include:
- Direct, one-pot sequential reductive alkylation of lactams/amides with Grignard and organolithium reagents through lactam/amide activation. (137 citations)
- Orphan nuclear receptor TR3 acts in autophagic cell death via mitochondrial signaling pathway (130 citations)
- Direct Transformation of Secondary Amides into Secondary Amines: Triflic Anhydride Activated Reductive Alkylation† (115 citations)
What are the main themes of his work throughout his whole career to date?
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.
He most often published in these fields:
- Stereochemistry (52.86%)
- Enantioselective synthesis (48.44%)
- Organic chemistry (47.92%)
What were the highlights of his more recent work (between 2016-2021)?
- Combinatorial chemistry (18.49%)
- Catalysis (9.90%)
- Organic chemistry (47.92%)
In recent papers he was focusing on the following fields of study:
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.
Between 2016 and 2021, his most popular works were:
- Dual catalysis for enantioselective convergent synthesis of enantiopure vicinal amino alcohols. (37 citations)
- Ni-Catalyzed cross-coupling reactions of N-acylpyrrole-type amides with organoboron reagents (25 citations)
- Direct Transformations of Amides: Tactics and Recent Progress (23 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Enzyme
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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