已发表成果:
WOK 论文 272 篇;中文核心 26 篇;其它论文 13 篇;专利发明 28 个;图书及章节 8 本;
Evans' Chiral Auxiliary-Based Asymmetric Synthetic Methodology and Its Modern Extensions
Ir-catalyzed Vinylogous Aldol-type Condensation Reactions between Tertiary Amides and Siloxyfuran: the Synthesis of γ-Benzylidenebutenolides
Research Progress of Active Colloidal Motors and Their Application Perspective in Electromagnetic Wave Absorption
Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids
Heteroaromatization and nickel catalysis enabled decarbamoylative arylations and borylations of tertiary amides
One-pot synthesis of 1,3-oxazin-4-ones through an Ir-catalyzed mild formal condensation reaction of secondary amides with acyl chlorides
Redox-Neutral Synthesis of α-Iminonitriles, α-Cyanoenamines, and <i>N</i>-Acyl Derivatives from Amides
Iridium and B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub> co-catalyzed chemoselective deoxygenative reduction of tertiary amides: application to the efficient synthesis and late-stage modification of pharmaceuticals
Concise, three-step enantioselective total synthesis of (4S,5S)-4-hydroxy-5-octylpyrrolidin-2-one, a colibactin pathway metabolite
Concise Total Synthesis of (-)-Quinocarcin Enabled by Catalytic Enantioselective Reductive 1,3-Dipolar Cycloaddition of Secondary Amides
Multicatalysis protocol enables direct and versatile enantioselective reductive transformations of secondary amides
Multicatalysis protocol enables direct and versatile enantioselective reductive transformations of secondary amides
A flexible enantioselective approach to 2,5-disubstituted cis-decahydroquinolines
Ir-Catalyzed Chemoselective Reductive Condensation Reactions of Tertiary Amides with Active Methylene Compounds
One-Pot Synthesis of alpha-Amino Bisphosphonates from Nitriles via Tf2O/HC(OR)(3)-Mediated Interrupted Ritter-Type Reaction
Tandem-catalysis-enabled highly chemoselective deoxygenative alkynylation and alkylation of tertiary amides: a versatile entry to functionalized alpha-substituted amines
Catalyst- and solvent-free aminolysis of the asymmetric derivatives of Evans' chiral N-acyloxazolidinones: enantioselective synthesis of chiral amides and its applications
Tf2O-Promoted Morgan-Walls Reaction: From a Flexible Approach to Functionalized Phenanthridines and Quinazolines to the Short and Divergent Total Syntheses of Alkaloids
Enantioselective total syntheses of marine natural products (+)-cylindricines C, D, E and their diastereomers
SmI2/Sm-Arylboronic Esters Combination for the Reductive Arylation of Aromatic Tertiary Amides
Enantioselective Total Syntheses of the Proposed and Revised Structures of Methoxystemofoline: A Stereochemical Revision
A versatile approach to functionalized cyclic ketones bearing quaternary carbon stereocenters via organocatalytic asymmetric conjugate addition of nitroalkanes to cyclic beta-substituted alpha,beta-Enones
Functional maturation of immature beta cells: A roadblock for stem cell therapy for type 1 diabetes
Photoredox-Catalyzed Decarboxylative Cross-Coupling of alpha-Amino Acids with Nitrones
Synthesis of 5-(1-Alkoxyalkylidene)tetronates by Direct Condensation Reactions of Tetronates with Thionolactones and Thionoesters
Organocatalytic Asymmetric Synthesis of an Advanced Intermediate of (+)-Sarain A
Enantioselective Reductive Cyanation and Phosphonylation of Secondary Amides by Iridium and Chiral Thiourea Sequential Catalysis
Chemoselective Reactions of Isocyanates with Secondary Amides: One-Pot Construction of 2,3-Dialkyl-Substituted Quinazolinones
Tf2O/TTBP (2,4,6-Tri-tert-butylpyrimidine): An Alternative Amide Activation System for the Direct Transformations of Both Tertiary and Secondary Amides
Asymmetric Deoxygenative Alkynylation of Tertiary Amides Enabled by Iridium/Copper Bimetallic Relay Catalysis
Tf2O-Mediated Cyclization of 7-Enamides: Bioinspired Construction of Fused Eight-Membered Carbocyclic Enimines and Enones
Catalytic Asymmetric Total Synthesis of Macrocyclic Marine Natural Product (-)-Haliclonin A
Exploratory Studies on a New Strategy for the Asymmetric Total Synthesis of the Arrow Poison-Frog Alkaloid Batrachotoxin: Asymmetric Synthesis of a Functionalized CD Ring
Malie acid-A Versatile Chiral Building Block in the Enantioselective Total Synthesis of Natural Products and in Synthetic Methodologies
Procedure-Economical, Enantioselective Total Syntheses of Polycyclic Natural Products and Analogues Containing a 3a-Hydroxyhexahydropyrrolo[2,3-b]indole-2-carboxylic Acid Residue
Enantioselective total syntheses of (+)-stemofoline and three congeners based on a biogenetic hypothesis
Two-Step Catalytic Transformation of N-Benzyllactams to Alkaloids (+/-)-Solenopsin, (+/-)-Solenopsin A, and (+)-Julifloridine
Amides as surrogates of aldehydes for C-C bond formation: amide-based direct Knoevenagel-type condensation reaction and related reactions
Concise, enantioselective total syntheses of both the proposed and revised structures of (-)-versiquinazoline H
Ni-catalyzed direct alcoholysis of N-acylpyrrole-type tertiary amides under mild conditions
Catalytic diastereoselective and enantioconvergent C(sp(3))-C(sp(3)) cross-coupling of racemic partners
Tf2O-Mediated Intermolecular Coupling of Secondary Amides with Enamines or Ketones: A Versatile and Direct Access to beta-Enaminones
Organocatalytic, Enantioselective Reductive Bis-functionalization of Secondary Amides: One-Pot Construction of Chiral 2,2-Disubstituted 3-Iminoindoline
Photoredox Catalysis for the Coupling Reaction of Nitrones with Aromatic Tertiary Amines
Cross-Coupling of Secondary Amides with Tertiary Amides: The Use of Tertiary Amides as Surrogates of Alkyl Carbanions for Ketone Synthesis
Ketone Synthesis by Direct, Orthogonal Chemoselective Hydroacylation of Alkenes with Amides: Use of Alkenes as Surrogates of Alkyl Carbanions
Double Addition of Alkynyllithium Reagents to Amides/Lactams: A Direct and Flexible Synthesis of 3-Amino-1,4-diynes Bearing an Aza-Quaternary Carbon Center
Chemoselective Synthesis of alpha-Amino-alpha-cyanophosphonates by Reductive Gem-Cyanation-Phosphonylation of Secondary Amides
Biomimetic Enantioselective Total Synthesis of (?)-Robustanoids A and B and Analogues
Multi-destination Map Layout Generation Based on Rigid Deformation
A Stepwise Annulation for the Transformation of Cyclic Ketones to Fused 6 and 7-Membered Cyclic Enimines and Enones
Construction of multifunctional heterocycles bearing aza-quaternary carbons by titanocene-catalyzed umpolung reactions
Ir-catalyzed chemoselective reduction of beta-amido esters: A versatile approach to beta-enamino esters
Intermolecular Dehydrative [4+2] Aza-Annulation of N-Arylamides with Alkenes: A Direct and Divergent Entrance to Aza-Heterocycles
Enamines as Surrogates of Alkyl Carbanions for the Direct Conversion of Secondary Amides to alpha-Branched Ketones
Rapid Generation of Molecular Complexity by Chemical Synthesis: Highly Efficient Total Synthesis of Hexacyclic Alkaloid (-)-Chaetominine and Its Biosynthetic Implications
Progress in Heterocycles-Based Asymmetric Vinylogous Mannich Reactions and Applications to the Synthesis of Alkaloids
Iridium-Catalyzed Reductive Alkylations of Secondary Amides
Unified strategy for step-economical and enantioselective total synthesis of all members of chaetominine natural products
Catalytic direct transformation of amides and imides: Useful chemistry for medicinal chemistry and natural product synthesis
Asymmetric Total Synthesis and Absolute Configuration Determination of (-)-Verrupyrroloindoline
The iridium-catalysed reductive coupling reaction of tertiary lactams/amides with isocyanoacetates
Palladium-Catalyzed [3+2]-C C/N C Bond-Forming Annulation
SmI2 and Titanocene-Mediated Coupling Reactions of alpha-Aminoalkyl Radicals and Applications to the Synthesis of Aza-Heterocycles
Direct Transformations of Amides: Tactics and Recent Progress
Chemoselective direct reductive trifluoromethylation of amides: a flexible access to functionalized alpha-trifluoromethylamines
Enamines as Surrogates of Alkene Carbanions for the Reductive Alkenylation of Secondary Amides: An Approach to Allylamines
Dual catalysis for enantioselective convergent synthesis of enantiopure vicinal amino alcohols
Versatile One-Pot Synthesis of Polysubstituted Cyclopent-2-enimines from α,β-Unsaturated Amides: Imino-Nazarov Reaction
Metal-free synthesis of quinolines by direct condensation of amides with alkynes: revelation of N-aryl nitrilium intermediates by 2D NMR techniques
Ni-Catalyzed cross-coupling reactions of N-acylpyrrole-type amides with organoboron reagents
Analogues of the 2-carboxyl-6-hydroxyoctahydroindole (CHOI) unit from diverging Pd-catalyzed allylations: Selectivity as a function of the double bond position
Substrate-Controlled Chemoselective Reactions of Isocyanoacetates with Amides and Lactams
Chemoselective direct transformation of common amides: The chemistry for medicinal chemistry and total synthesis of natural products
Enantioselective total synthesis of the alkaloid (-)-haliclonin A
An attempted approach to the tricyclic core of haliclonin A: Structural elucidation of the final product by 2D NMR
Direct Reductive Cyanation of A 2-Pyrrolidinone Chiral Building Block Bearing An Unprotected Hydroxyl Group: A Stereoselective Synthesis of N-Methyl-2-epi-bulgecinine
Further Studies on the Direct Synthesis of alpha, beta-Unsaturated Ketimines and alpha, beta-Enones by Chemoselective Dehydrative Addition of Functionalized Alkenes to Secondary Amides
A Direct, Versatile, and Chemoselective Synthesis of Vinylogous Bis- and Monourethanes/amides and beta-Keto Esters by Aza-Knoevenagel-Type Reactions of Tertiary Amides with Enolates
One-pot synthesis of N-heterocycles and enimino carbocycles by tandem dehydrative coupling-reductive cyclization of halo-sec-amides and dehydrative cyclization of olefinic sec-amides
One-Pot Reductive 1,3-Dipolar Cycloaddition of Secondary Amides: A Two-Step Transformation of Primary Amides
Tf2O-TMDS combination for the direct reductive transformation of secondary amides to aldimines, aldehydes, and/or amines
Metal-Free Intermolecular Coupling of Arenes with Secondary Amides: Chemoselective Synthesis of Aromatic Ketimines and Ketones, and N-Deacylation of Secondary Amides
Metal-Free C-H Alkyliminylation and Acylation of Alkenes with Secondary Amides
Studies on the Second-Generation Approach to Loline Alkaloids: Synthesis of N -Bus-norloline through N - Tert -Butanesulfinyl Imine Based Asymmetric Vinylogous Mannich Reaction
Mild Metal-Free Hydrosilylation of Secondary Amides to Amines
Enantioselective Total Synthesis and Structural Revision of (-)-Isochaetominine
Organocatalytic, Asymmetric Total Synthesis of (-)-HalicloninA
A versatile access to vicinal diamine motifs by highly anti-selective asymmetric vinylogous Mannich reactions: an efficient total synthesis of (+)-absouline
Chemoselective reductive alkynylation of tertiary amides by Ir and Cu(I) bis-metal sequential catalysis
The asymmetric total synthesis of (+)-N-acetyl norloline
Stereodivergent and enantioselective total syntheses of isochaetominines A-C and four pairs of isochaetominine C enantiomers: a six-step approach
Titanocene(III)-Catalyzed Three-Component Reaction of Secondary Amides, Aldehydes, and Electrophilic Alkenes
Mild N-deacylation of secondary amides by alkylation with organocerium reagents
Induction of Autophagic Death in Cancer Cells by Agonizing TR3 and Attenuating Akt2 Activity
Direct Transformation of Amides: Reductive Cycloaddition of Secondary Amides with Danishefsky Diene
A general method for the one-pot reductive functionalization of secondary amides
The first enantioselective total synthesis of (+)-preussin B and an improved synthesis of (+)-preussin by step-economical methods
SmI2-mediated radical coupling strategy to securinega alkaloids: Total synthesis of (-)-14,15-dihydrosecurinine and formal total synthesis of (-)-securinine
Simple, versatile, and chemoselective reduction of secondary amides and lactams to amines with the Tf2O-NaBH4 or Cp2ZrHCl-NaBH4 system
Studies on the asymmetric synthesis of pandamarilactonines: an unexpected syn-selective vinylogous Mannich reaction of N-tert-butanesulfinimines
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 beta,beta-difunctionalized enamines
Tertiary amide-based Knoevenagel-type reactions: a direct, general, and chemoselective approach to enaminones
Efficient asymmetric syntheses of alkaloids and medicinally relevant molecules based on heterocyclic chiral building blocks
Sulindac-Derived RXR alpha Modulators Inhibit Cancer Cell Growth by Binding to a Novel Site
A concise formal stereoselective total synthesis of (-)-swainsonine
Orphan nuclear receptor TR3 acts in autophagic cell death via mitochondrial signaling pathway
A novel and versatile method for the enantioselective syntheses of tropane alkaloids
The four-step total synthesis of (-)-chaetominine
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
Complexity generation by chemical synthesis: a five-step synthesis of (-)-chaetominine from L-tryptophan and its biosynthetic implications
Towards stereochemical control: A short formal enantioselective total synthesis of pumiliotoxins 251D and 237A
General One-Pot Reductive gem-Bis-Alkylation of Tertiary Lactams/Amides: Rapid Construction of 1-Azaspirocycles and Formal Total Synthesis of (+/-)-Cephalotaxine
Modular Enantioselective Synthesis of 8-Aza-prostaglandin E-1
A direct and general method for the reductive alkylation of tertiary lactams/amides: Application to the step economical synthesis of alkaloid (-)-morusimic acid D
Chiral imidazo[1,5-a]tetrahydroquinoline N-heterocyclic carbenes and their copper complexes for asymmetric catalysis
Umpolung of Hemiaminals: Titanocene-Catalyzed Dehydroxylative Radical Coupling Reactions with Activated Alkenes
SmI2-Mediated Intermolecular Coupling of gamma-Lactam N-alpha-Radicals with Activated Alkenes: Asymmetric Synthesis of 11-Hydroxylated Analogues of the Lead Compounds CP-734432 and PF-04475270
Enantioselective total syntheses of (-)-FR901483 and (+)-8- epi -FR901483
Total synthesis of (-)-sessilifoliamide J
Toward the total synthesis of haliclonin a: Construction of a tricyclic substructure
Versatile construction of functionalized tropane ring systems based on lactam activation: enantioselective synthesis of (+)-pervilleine B
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
A Concise and Divergent Approach to Hydroxylated Piperidine Alkaloids and Azasugar Lactams
Synthesis and SAR study of modulators inhibiting tRXR alpha-dependent AKT activation
The orphan nuclear receptor Nur77 regulates LKB1 localization and activates AMPK
Asymmetric Syntheses of the Sex Pheromones of Pine Sawflies, Their Homologs and Stereoisomers
General Direct Transformation of Secondary Amides to Ketones via Amide Activation
A Formal Enantioselective Total Synthesis of FR901483
Reductive hydroxyalkylation/alkylation of amines with lactones/esters
Direct transformation of secondary amides into secondary amines: Triflic anhydride activated reductive alkylation
Progress on the total synthesis of natural products in China: From 2006 to 2010
JSPS Asian Core Program: Cutting-edge organic chemistry in Asia (phase II), 14th Asian Chemical Congress, and IUPAC Joint Workshop: Strategic planning for a new east and southeast Asian network for organic chemistry
Enantioselective syntheses of rigidiusculamides A and B: Revision of the relative stereochemistry of rigidiusculamide A
One-pot reductive coupling of N-acylcarbamates with activated alkenes: Application to the asymmetric synthesis of pyrrolo[1,2-a]azepin-5-one ring system and (-)-xenovenine
Asymmetric Synthesis of Both Enantiomers of Disparlure
Concise Asymmetric Total Synthesis of 9-epi-Sessilifoliamide J
Asymmetric Vinylogous Mannich Reactions: A Versatile Approach to Functionalized Heterocycles
Diastereoselective synthesis and bioactivity of long-chain anti-2-amino-3-alkanols
A study on the racemization step in the synthesis of pyrrolidinols via cyclic alpha-hydrovimides
A Flexible Approach to Protected (4S,5S)-5-Alkyl-1-benzyl-4-benzyloxy-2-pyrrolidinones
Amide Activation by Tf2O: Reduction of Amides to Amines by NaBH4 under Mild Conditions
Asymmetric synthesis of the cytotoxic marine natural product (+)-awajanomycin and its C-11 epimer
NSAID Sulindac and Its Analog Bind RXR alpha and Inhibit RXR alpha-Dependent AKT Signaling
A Unique Pharmacophore for Activation of the Nuclear Orphan Receptor Nur77 In vivo and In vitro
Asymmetric syntheses of 6-deoxyfagomin, D-deoxyrhamnojirimycin, and D-rhamnono-1,5-lactam
Asymmetric Total Synthesis of (-)-Awajanomycin
Enantioselective synthesis of the R-enantiomer of the feeding deterrent (S)-ypaoamide
Generation and α-hydroxyalkylation of a novel 3-piperidinol N-α-carbanion intermediate
An enantioselective synthesis of (+)-azimic acid
FACILE SYNTHESES OF THREE AHP-TYPE BUILDING BLOCKS WITH COMPLEMENTARY REACTIVITIES
A Flexible Approach to Methyl (5S)-5-Alkyltetramate Derivatives
New and Concise Approach to (R)-alpha-Lipoic Acid
One-pot cross-coupling of N-acyl N,O-acetals with alpha,beta-unsaturated compounds
ORGN 67-Flexible approaches for the asymmetric synthesis of bioactive alkaloids
A new approach for the asymmetric synthesis of (2S,3S)-3-hydroxypipecolic acid
First asymmetric synthesis of piperidine alkaloid (-)-morusimic acid D
A concise approach to (+)-1-epi-castanospermine
A new synthesis of alkaloid (S)-3-hydroxypiperidin-2-one and its O-TBS protected derivative
A divergent asymmetric approach to aza-spiropyran derivative and (1S, 8aR)-1-hydroxyindolizidine
Syntheses of enantio-enriched chiral building blocks from L-glutamic acid
A versatile approach to protected (4S,5R)-4-hydroxy-5-(alpha-hydroxyalkyl)-2-pyrrolidinones
A new approach for the asymmetric syntheses of 2-epi-deoxoprosopinine and azasugar derivatives
Asymmetric synthesis of (S)-homocitric acid lactone
A flexible approach to (S)-3-amino-2-pyrrolidinone derivatives
Asymmetric synthesis of beta,gamma-disubstituted gamma-lactones
Enantioseparation of 3-substituted isoindolin-1-ones by HPLC
(2S,3S)-3-Hydroxy-1-(4-rnethoxybenzy1)-piperidine-2-carboxamide
An improved asymmetric synthesis of unusual amino acid (2S,3S)3-hydroxyproline
A practical two-step synthesis of 3-alkyl-2,3-dihydro-1H-isoindolin-1-ones
A versatile approach for the asymmetric synthesis of 3-alkyl-2,3-dihydro-1H-isoindolin-1-ones
Further studies on the reductive-alkylation of chiral endo-himimide derived from (R)-phenylglycinol
Asymmetric synthesis of antimalarial alkaloids (+)-febrifugine and (+)-isofebrifugine
Synthesis of (S)-vasicol and (S)-3-hydroxy-2-pyrrolidinone
A flexible approach to the gamma-amino-beta-hydroxy acid moiety of hapalosin
NMR and ESI-MS studies on the interactions between oxodiperoxooxalatovanadate and organic ligands
An improved formal total synthesis of (-)-anisomycin
Synthesis and Crystal Structure of (1R,2S,5R,8S,9R,10S)-8-Methyl-4-aza-5-phenyl-7-oxatetracyclo[8.2.1.0(2,9).0(4,8)]-11-en-3-one
A versatile approach for the asymmetric synthesis of 3-alkyl-isoindolin-1-ones
A new approach for asymmetric synthesis of (R)-3-methylpyrrolidine alkaloids from (S)-malic acid
Progress in the asymmetric synthetic methodology based on malimides
A new asymmetric synthesis of (R)-3-methylpyrrolidine alkaloids starting from (S)-malic acid
Some observations on the asymmetric reductive alkylation of cyclic imides
Asymmetric synthesis of 1,3-and 1,3,4-substituted pyrrolidines
Inhibition effects of some bioactive peroxovanadium complexes on the tyrosine phosphatase
Asymmetric synthesis of (-)-(R)-pyrrolam A starting from (S)-malic acid (vol 10, pg 3827, 1999)
An alternative stereoselective synthesis of protected trans-5-alkyl-4-hydroxy-2-pyrrolidinones
Asymmetric synthesis of (-)-(R)-pyrrolam A starting from (S)-malic acid
A new chiral synthesis of naturally occurring (-)-(S)-4-hydroxy-2-pyrrolidinone
A new approach to (S)-4-hydroxy-2-pyrrolidinone and its 3-substituted analogues
D-Quinic acid, a versatile chiron in organic synthesis
Enantioselective synthesis of pyrrolydinonyl thymine nucleoside analogues
Asymmetric synthesis of polyhydroxy pyrrolidinonyl nucleoside analogues from tartaric acid
Enantiomeric resolution of N, β, γ-trisubstituted-γ-lactams by HPLC on Chiralcel OB column
Diastereoisomeric separation of (R,S)-1,1 prime -binaphthalene-2, 2 prime -diol-mono-[(-)-menthyl] carbonate by RP-HPLC
NMR studies on [VS4-Cu-n] (n = 3, 4, 5, 6) clusters
A new approach to (-)-anisomycin
A versatile approach to the activated form of (3S, 4R)-statine and its analogues
A new catalyst for hydrogen transfer hydrogenation of acetophenone
Synthesis, Characterization and Catalytic Properties of New Diamino/Diphosphine Ruthenium Complexes
Studies on the asymmetric synthesis of pyrrolidine alkaloids and related compounds .1. Synthesis of a chiral precursor for preussin and AHPPA
alpha-Amidoalkylation via sulfones: Towards the synthesis of ant venom alkaloids
百部叶碱核心骨架新合成策略探索:含三个连续手性中心双环中间体的对映选择性构筑
中国科学:化学,1674-7224,2023-03-20.基于SmI2/Sm-芳基硼酸酯组合的芳香叔酰胺还原芳基化
有机化学,0253-2786,2021-09-25.天然产物的仿生全合成:回顾与展望
厦门大学学报(自然科学版),0438-0479,2021-03-28.苹果酸——天然产物对映选择性全合成和合成方法学中多用途的手性合成砌块
化学进展,1005-281X,2020-11-05.箭毒蛙生物碱Batrachotoxin的不对称全合成新策略初探——官能化的CD环的不对称合成
有机化学,0253-2786,2020-08-12.光催化氧化还原体系中硝酮与芳香叔胺的自由基偶联反应
化学学报,0567-7351,2019-09-15.酰胺直接转化:策略与近期进展
化学学报,0567-7351,2018.书评:《现代天然产物化学》
有机化学,0253-2786,2018.基于杂环的不对称插烯Mannich反应及其在生物碱合成中的应用进展
有机化学,0253-2786,2018.二碘化钐参与及二茂钛催化的氮α-位碳自由基偶联反应及其在含氮杂环合成中的应用
化学进展,1005-281X,2018.含未保护羟基2-吡咯烷酮衍生物的直接还原氰基化:N甲基-2-别-Bulgecinine的立体选择性合成
有机化学,0253-2786,2017-05-25.(—)-Isochaetominine推测结构的对映选择性全合成与结构修正
有机化学,0253-2786,2015-12-15.酰胺的直接转化:仲酰胺与丹尼谢夫斯基双烯的还原环加成反应
化学学报,0567-7351,2015-07-15.有机化学进展(2011~2012)
化学通报,0441-3776,2014-07-18.仲酰胺经酰胺活化直接合成酮的普适性方法
化学学报,0567-7351,2012.一个多用途吡咯烷类氮杂糖中间体的不对称合成
厦门大学学报(自然科学版),0438-0479,2011.(8R,8aS)-及(8R,8aR)-8-羟基-5-吲哚里西啶酮的不对称合成:两个有用的羟基吲哚里西啶合成砌块
中国科学:化学,1674-7224,2011.天然岩藻糖苷酶的抑制剂L-deoxygulojirimycin关键中间体的不对称合成
厦门大学学报(自然科学版),0438-0479,2006-09-30.β,γ-二取代γ-内酯的不对称合成
化学学报,0567-7351,2004-09-30.2,6-二-O-戊基-β-环糊精涂渍Symmetry C_8柱拆分扁桃酸及其类似物对映体
色谱,1000-8713,2004-07-30.手性高效液相色谱拆分3-取代异吲哚-1-酮的研究
高等学校化学学报,0251-0790,2004-06-15.两种3-甲基吡咯烷蚂蚁毒素的不对称合成
厦门大学学报(自然科学版),0438-0479,2004-01-30.手性二噁唑啉和二噁唑啉吡啶的合成
厦门大学学报(自然科学版),0438-0479,2003-11-30.手性二噁唑啉吡啶铁和镍配合物的制备与表征
无机化学学报,1001-4861,2003-11-01.草酸双过氧钒配合物与有机配体相互作用的NMR和ESI-MS研究
化学学报,0567-7351,2003-07-20.(1R,2S,5R,8S,9R,10S)-8-甲基-4-氮杂-5-苯基-7-氧杂四环[8.2.1.0~(2,9).0(~4,8)]十三-11-烯-3-酮的合成和晶体结构
结构化学,0254-5861,2003-03-25.铱催化叔酰胺与呋喃硅醚间的类插烯Aldol缩合反应:γ-亚苄基-丁烯酸内酯的合成
化学学报,0567-7351,2023-10-15.海洋天然产物Haliclonin A的有机催化不对称全合成
中国化学会第十一届全国天然有机化学学术会议论文集(第一册),,2016-09-25.大环生物碱Haliclonin A的首次不对称全合成
中国化学会第十一届全国天然有机化学学术会议论文集(第四册),,2016-09-25.仲酰胺直接转化化学
中国化学会第30届学术年会摘要集-第九分会:有机化学,,2016-07-01.3-羟基哌啶氮α-碳负离子的形成及α-羟烷化反应
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