Total Synthesis of Bioactive Natural Products

Diels-Alder reaction Hypericum perforatum Citrus fruits Claisen rearrangement Heck reaction Friedel-Crafts reaction Grignard reaction Epoxidation Cytotoxicity Coupling reaction Cross Metathesis Antibiotic Antioxidant Cytotoxic Hyperforin Antibacterial Anticancer Antiproliferative Antiviral Alkaloid Bombyx mori Antidepressant Antimicrobial Lignan Extra virgin olive oil Dess-Martin oxidation Cholesterol lowering Anti-tumor Antitumor Immunomodulatory Glycolipid 10-Membered macrolide (±)-3-Hydroxy-ß-ionone 3-Oxazolylindole alkaloid (+)-3-Oxo-a-ionol 5-Lipoxygenase inhibitor 7-Desmethoxyfusarentin 6-Deoxypladienolide D (-)-6-O-Desmethylantofine Ageladine A Agelas nakamurai Allelopathic Activity (+)-Ainsliadimer A Ainsliaea macrocephala [4 + 2]-Hetero-Diels-Alder dimerization Ancistrocladus ealaensis Allelopathic (-)-Andrographolide Amphidinium species (+)-Amphidinolide T1 Anogeissus acuminata Anti- Alzheimer’s antidiabetic (-)-Aiphanol Antipathogenic Anticanerous Antidengue Anti-HIV Ancistrotanzanine B Antitumor necrosis factor antagonism Anticancerous Antileishmanial Antrodia Camphorata Amide-Wittig olefination Aeruginosins 298-A and B Antimalarial Antiplatelet aggregation Bayer-Villiger oxidation Appel protocol Anolignan A Antiinflammatory Antileishmanials Anti-TMV Bauhinia purpurea Antrocamphin A Beilschmiedia kunstleri B. odoratissimum Bi-linderone Aiphanes aculeata Asymmetric Diels-Alder reaction Atroviridin Alder-Rickerts reaction Bisnorsesquiterpene A. tanzaniensis Austroplenckia populnea Baeyer-Villiger oxidation Bulbophylol-B Benzenoid Ancistroealaine A Basillus sp. strain B-60 Andrographis paniculata Brown allylation Birch reduction (+)-Chaetocin Anolignan B (+)-BINOL Chaetomium minutum Biomimetic cyclization Biphenyl ether derivative Bisnortriterpenoid Chugaev elimination Claisen cyclization Arenamide A Bauhinoxepin J Bischler-Napieralski reaction Corey-Bakshi-Shibata reduction Corey-Seabach umpolung method Barbier Reaction Cross-enyne metathesis Bombykol Cynanchum species Darzens reaction Dauben-Michno oxidative rearrangement Brown crotylation Diels-Alder cycloaddition Bulbophyllum kwangtungense Crabtree’s catalyst Daedalea dickinsii Danheiser’s protocol Caminoside A Caminus sphaeroconia Epidithiodiketopiperazine (ETP) alkaloid ent-Labdane diterpenoid Eschenmoser’s salt Dihydroisocoumarins Chromene-derivative Ciliatamides A and B Cyclooxygenases inhibitory activity Daedalin A Dictamnus dasycarpus Dienamide Clusia rosea Friedlander condensation Gliocladium roseum Cope rearrangement Furukawa cyclopropanation (+)-Harziphilone Cyclohexadepsipeptide f]oxepin Cyclopentenedione Hibarimicinone Croton steenkampianus Cylindol A Hünig''s base (+)-Gliocladin B Dess-Martin periodinane Dess-Martin periodinane oxidation Dihydrodibenz[b Integric acid Diterpenoid D-Hpla Intramolecular Dieckmann condensation Horner-Wadsworth-Emmons reaction Heat-shock protein 90 (HSP90) inhibitor Heck coupling Johnson-Claisen rearrangement Horner-Wardsworth-Emmons olefination Ito-Saegusa oxidation Ley oxidation Kumada-Tamao-Corriu coupling (±)-Marinopyrrole A L. erythrocarpa (±)-Limonin Lindera lucida Etnangien Evans-Carreria method Jones oxidation Karalicin (-)-Kunstleramide Kirschleger’s reaction L-Argol L-Choi Ley-Griffith oxidation Lindera aggregata Lindlar’s condition Linderaspirone A Garcinia atroviridis Herpes Simplex Virus 1 (HSV1) inhibitor Hepatoprotective (±)-Paecilomycine A Indole acyloin Jineol QUINOLINE ALKALOID (±)-Steenkrotin A (+)-Sattazolin Horner-Wadsworth-Emmon reaction Hoveyda-Grubbs catalyst Hoveyda-Grubbs second-generation catalyst (-)-Stagonolide A Imperata Cylindrica (+)-Xylarenal A Limonoid (tetranortriterpenoid) (-)-Oleocanthal (-)-Melotenine A Aaptos ciliata