Description
Royal Society Targets in Heterocyclic Systems Volume 12 2009 Edition by Orazio A Attanasi, Domenico Spinelli
Volume 12 (2008) keeps the international standard of the THS series and contains fifteen chapters, covering the synthesis, reactivity, activity (including medicinal) and mass spectrometry of different heterorings. Written by contributing authors from Brazil, Egypt, France, Germany, Italy, Poland, Portugal, Russia and Switzerland the volume facilitates a valuable international perspective on Heterocyclic derivatives and their consequential role in organic chemistry in the construction of more complicated molecules. Volume 11 (2008) will be welcomed by researchers and industrialists with an interest in the synthesis, reactivity, activity (including medicinal) and mass spectrometry of different heterorings. Table of contents :- Synthetic accessibility to protophorphyrin-IX, chlorophyll a and (2R)-phytochromobilin and 1other biologically important pyrrole derivatives in any 13C and 15N enriched isotopic form; a-Alkilidene-b-lactones and lactams via radical- and transition metal-mediated cyclizations; The reaction of carbonyl compounds and nitriles with triflic anhydride. Synthesis of pyrimidines, benzothiazines, oxazoles and triazines; Metal-mediated CuC and CuN bond formation in the stnthesis of bioactive purines; Indole phytoalexins from brassicaceae: synthesis and anticancer activity; Synthesis of phosphepines and application in asymmetric catalysis; Cyclic phospho di- and triester as structural elements of nucleic acids; Chemistry of biologically active carbolines; Meso-substituted porphyrin synthesis from monopyrrole: an overview; 1,2- And 1,3-oxazolopyridines: versatile building blocks for the heterocyclic synthesis; New methods for the asymmetric synthesis of piperidines and pyrrolidines: chiral auxiliaries and asymmetric organocatalysis; Synthesis of phosphorus-substituted sulfur heterocycles; Carbolithiation reactions in the synthesis of heterocycles; Oligo- and poly(2,5-thienylene-ethynylene)s; Chemoenzymatic synthesis of optically active pyridine derivatives; Asymmetric synthesis of substituted piperazines; Microwave assisted synthesis of functional oligothiopenes