Chemistry of Pyrroles
Autor Boris A. Trofimov, Al'bina I. Mikhaleva, Elena Yu Schmidt, Lyubov N. Sobeninaen Limba Engleză Paperback – 16 noi 2016
The authors analyze conditions of typical syntheses, limitations of their applicability, and possibility of vinyl chloride or dichloroethane application instead of acetylene. They examine chemical engineering aspects of the first synthesis of tetrahydroindole and indole from commercially available oxime of cyclohexanone and acetylene. In addition, the book discusses new facets of pyrroles and N-vinyl pyrroles reactivity in the reactions with the participation of both the pyrrole ring and N-vinyl groups.
The book provides condensed, clear-cut information on novel syntheses of substituted pyrroles as key structural units of living matter (chlorophyll and hemoglobin), pharmaceuticals, and monomers for optoelectronic materials. It includes tables that provide references to original works, forming a guide to a variety of the reactions and synthesized compounds discussed. With coverage of the broad range of pyrrole chemistry and methods for their synthesis, it provides both a theoretical and an experimental basis for drug design.
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Specificații
ISBN-13: 9781138034020
ISBN-10: 1138034029
Pagini: 398
Ilustrații: 444
Dimensiuni: 156 x 234 mm
Greutate: 0.45 kg
Ediția:1
Editura: CRC Press
Colecția CRC Press
Locul publicării:Boca Raton, United States
ISBN-10: 1138034029
Pagini: 398
Ilustrații: 444
Dimensiuni: 156 x 234 mm
Greutate: 0.45 kg
Ediția:1
Editura: CRC Press
Colecția CRC Press
Locul publicării:Boca Raton, United States
Cuprins
Introduction. Synthesis of Pyrroles and N-Vinylpyrroles by the Reaction of Ketones (Ketoximes) with Acetylenes. Heterocyclization of ketoximes with acetylene. Regioselectivity of the reaction. Substituted acetylenes in reactions with ketoximes. Vinyl halogenides and dihalogenethanes as synthetic equivalents of acetylene . Intermediate stages and side reactions. δ-Carbolines from 3-acylindoles and acetylene. Reaction of ketoximes with acetylene in the presence of ketones. One-pot assembly of 4-methylen-3-oxa-1-azabicyclo[3.1.0]hexanes. Transformations of aldoximes in the systems MOH/DMSO and MOH/DMSO/acetylene. Mechanism of pyrrole synthesis from ketoximes and acetylene. Novel Aspects of NH- and N-Vinylpyrroles Reactivity. Reaction with the participation of the pyrrole ring. Reactions with participation of the vinyl group. Conclusions. References. Index.
Notă biografică
Boris A. Trofimov, Al'bina I. Mikhaleva, Elena Yu Schmidt, Lyubov N. Sobenina
Descriere
Pyrrole is a heterocyclic aromatic organic compound. The book is devoted to the latest achievements of the chemistry of pyrrole, a fundamental structural unit with vitally important molecular systems (chlorophyll and hemoglobin), natural hormones, antibiotics, pigments, and pheromones. The book provides condensed, clear-cut information on novel syntheses of substituted pyrroles as key structural units of living matter (chlorophyll and hemoglobin), pharmaceuticals, and monomers for optoelectronic materials.