Lead Optimization of Butyrolactone I as an Orally Bioavailable Antiallergic Agent Targeting FcγRIIB

Synthetic Studies toward Pseudolaric Acids: Radical Cyclization to Form Bridged Scaffold

Divergent Total Syntheses of <i>Illicium</i> Sesquiterpenes through Late-Stage Skeletal Reorganization

Synthesis of Clionastatins A and B through Enhancement of Chlorination and Oxidation Levels of Testosterone

Two-Stage Syntheses of Clionastatins A and B

Unexpected Pyridinyl Group Mediated Metal-Free Wacker-Type Oxidation en Route to Pyrido[2,1-a ]isoindol-5-ium Salts

Total Synthesis and Assignment of the Absolute Configuration of (+)-Omphalic Acid

Site-Specific Photochemical Desaturation Enables Divergent Syntheses of Illicium Sesquiterpenes

Divergent total syntheses of pseudoberberine and nitidine through C-H vinylation and switchable 6 pi electrocyclizations

Synthetic studies towards atkamine

Merging C-H Vinylation with Switchable 6 pi-Electrocyclizations for Divergent Heterocycle Synthesis

Structure-Activity Relationship Study Enables the Discovery of a Novel Berberine Analogue as the RXR alpha Activator to Inhibit Colon Cancer

Recent progress in the total synthesis of marine brominated sesquiterpene aplydactone

Conformational Design Principles in Total Synthesis

Nesteretal A, A Novel Class of Cage-Like Polyketide from Marine-Derived Actinomycete Nesterenkonia halobia

Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: Synthesis of the tricyclic core of pseudolaric acid F

Divergent total syntheses of five illudalane sesquiterpenes and assignment of the absolute configuration

Cycloaddition/annulation strategies for the construction of multisubstituted pyrrolidines and their applications in natural product synthesis

Enantioselective total synthesis of periconiasin A

Asymmetric Total Synthesis of (+)-Majusculoic Acid via a Dimerization-Dedimerization Strategy and Absolute Configuration Assignment

Conformational Bias by a Removable Silyl Group: Construction of Bicyclo[n.3.1]alkenes by Ring Closing Metathesis

Total Synthesis of Aplydactone by a Conformationally Controlled C-H Functionalization

Synthesis of beta-prolinols via [3+2] cycloaddition and one-pot programmed reduction: Valuable building blocks for polyheterocycles

Total Synthesis of (+)-Fusarisetin A Driven by a One-Pot Four-Reaction Process

Recent Progress in the Synthesis of 5-Unsubstituted Pyrrolidines via [3+2] Cycloadditions

Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4+1] Annulation toward Multisubstituted Tetrahydrofurans

The Cyano Group as a Traceless Activation Group for the Intermolecular [3+2] Cycloaddition of Azomethine Ylides: A Five-Step Synthesis of (±)-Isoretronecanol

Diastereoselective total synthesis of (卤)-schindilactone A, Part 1: Construction of the ABC and FGH ring systems and initial attempts to construct the CDEF ring system