• A new 22,26-seco physalin steroid from Physalis angulata
• Uvarmicranones A and B, two new benzoquinones and cytotoxic constituents from the stems of Uvaria micrantha (A. DC.) Hook. f. & Thomson
• Vernodalidimer L, a sesquiterpene lactone dimer from Vernonia extensa and anti-tumor effects of vernodalin, vernolepin, and vernolide on HepG2 liver cancer cells
• A Concise Approach to Oxo-Dehydrorotenoid by Direct Lactonization and the Total Syntheses of Stemonone, Rotenonone, 6-Oxo-dehydroelliptone, and 6-Oxo-6a,12a-dehydrodeguelin
• Cytotoxic and antimicrobial labdane and clerodane diterpenoids from Kaempferia elegans and Kaempferia pulchra
• Roscotanes and roscoranes: Oxygenated abietane and pimarane diterpenoids from Kaempferia roscoeana
• Superbanone, A New 2-Aryl-3-benzofuranone and Other Bioactive Constituents from the Tube Roots of Butea superba
• Ailanthusins A-G and nor-lupane triterpenoids from Ailanthus triphysa
• DBU-mediated regioselective intramolecular cyclization/dehydration of ortho diketo phenoxyethers: A synthesis of 2,3-substituted γ-benzopyranones
• Structural study on a naturally occurring terphenyl quinone
• Cycloaddition across the benzofuran ring as an approach to the morphine alkaloids
• Total synthesis of (±)-Strychnine via a [4 + 2] cycloaddition/ rearrangement cascade
• A Rh(II)-catalyzed cycloaddition approach toward the synthesis of komaroviquinone
• A general synthetic entry to the pentacyclic Strychnos alkaloid family, using a [4 + 2]-cycloaddition/rearrangement cascade sequence
• N,O-heterocycles as synthetic intermediates
• An approach toward oxidopyrylium ylides using Rh(II)-catalyzed cyclization chemistry
• Total synthesis of (±)-strychnine via a [4 + 2]-cycloaddition/ rearrangement cascade
• Efficient construction of the oxatricyclo[6.3.1.0^0,0]dodecane core of komaroviquinone using a cyclization/cycloaddition cascade of a rhodium carbenoid intermediate
• Synthesis of sedamine by tethered cyclofunctionalisation
• A target site for template-based design of measles virus entry inhibitors
• The pyridinium reduction route to alkaloids: A synthesis of (±)-tashiromine