13th International Conference on Organic Synthesis (ICOS-13), Warsaw, Poland, 1–5 July 2000
This conference is part of the Organic Synthesis series.
Formylation of carbohydrates and the evolution of synthetic routes to artificial oligosaccharides and glycoconjugates
Glyoxylic acid derivatives in asymmetric synthesis
Designing efficient synthetic routes to polyfunctionality
New developments in radical chemistry. Applications to total synthesis and asymmetric processes
Application of directed evolution in the development of enantioselective enzymes
Stereoselective C,C-bond formation. Cyclizations of biradicals
Total synthesis of herboxidiene, a complex polyketide from Streptomyces species A7847
Synthetic studies toward pyranonaphthoquinone antibiotics
Allylic boron and zinc derivatives in synthesis and transformations of nitrogen heterocycles
Vinylogous aldol reaction of heterocyclic silyloxy dienes. Application in synthesis
Fluorous methods for synthesis and separation of organic molecules
Hypervalent siloxane derivatives. An alternative to Stille and Suzuki couplings
Synthetic studies on the A83586C and bryostatin antitumor macrolides and the monamycin antibiotics
Stereoselective and enantioselective synthesis of five-membered rings via conjugate additions of allylsulfone carbanions
Ring constructions by the use of fluorine substituent as activator and controller
Stereocontrolled asymmetric synthesis
Selective transformations mediated by main-group organometallics
New nucleoside analogs, synthesis, and biological properties
Reactions involving inorganic compounds
Titanacyclopropanes as versatile intermediates for carbon-carbon bond formation in reactions with unsaturated compounds
Oxazoline-N-oxide mediated asymmetric cycloadditions. Recent progress in the stereo-selective syntheses of β-lactones and β-lactams
Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, P. R. China
Bicyclopropylidene. A unique tetrasubstituted alkene and versatile C6-building block for organic synthesis
Gary A. Molander
Versatility of β-lactams in synthesis. Studies directed toward the synthesis of complex nucleoside antibiotics and some macrocyclic peptides
From phosphatriafulvenes to phosphabenzenes and stable
six-membered phosphaallenes
Anionic cyclization approach toward perhydroindoles. Total synthesis of montanine-type Amaryllidaceae alkaloids
Stereochemical support for Serratia endonuclease active-site geometry
Synthetic study of ravidomycin, a hybrid natural product
Use of visible light. Second-generation titanium oxide photocatalysts prepared by the application of an advanced metal ion-implantation method
Selective monomethylation reactions of methylene-active compounds with dimethylcarbonate. An example of clean synthesis