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A01=Al'bina I. Mikhaleva
A01=Boris A. Trofimov
A01=Elena Yu Schmidt
A01=Lyubov N. Sobenina
Acetophenone Oxime
acetylene
advanced pyrrole ring construction
Age Group_Uncategorized
Age Group_Uncategorized
alkali
Alkali Metal
Alkali Metal Cations
Alkali Metal Hydroxides
Aqueous DMSO
Atom C4
Author_Al'bina I. Mikhaleva
Author_Boris A. Trofimov
Author_Elena Yu Schmidt
Author_Lyubov N. Sobenina
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Back Donation
C5 Atom
Catalytic Hydrogenation
Category1=Non-Fiction
Category=PNN
cations
Contact Ion Pair
COP=United States
cyclohexanone
Cyclohexanone Oxime
Delivery_Pre-order
DMSO
DMSO and MOH
DMSO System
eq_bestseller
eq_isMigrated=2
eq_nobargain
eq_non-fiction
eq_science
halide
HC CH
heterocyclic chemistry
Heterocyclization of ketoximes with acetylene
hydrogen
Hydrogen Halides
hydroxylic
Hydroxylic Solvent
indole formation process
Ketone Oximation
KOH Concentration
Language_English
metal
MOH
NH2OH HCl
Novel Aspects of NH- and N-Vinylpyrroles Reactivity
optoelectronic material precursors
organic synthesis methods
oxime
PA=Temporarily unavailable
pharmaceutical compound synthesis
Price_€100 and above
PS=Active
Pyrrole Ring
Pyrrole Synthesis
ring
Sodium Dodecylsulfonate
softlaunch
solvent
Solvent Separated Ion Pair
superbase catalysis
Synthesis of Pyrroles and N-Vinylpyrroles by the Reaction of Ketones (Ketoximes) with Acetylenes
Thiophene Ring
Transformations of aldoximes in the systems MOH
Transformations of aldoximes in the systems MOH/DMSO and MOH/DMSO/acetylene
Transformations of aldoximes in the systems MOHDMSO and MOHDMSOacetylene
Triple Bond
Vinyl halogenides and dihalogenethanes as synthetic equivalents of acetylene

Product details

  • ISBN 9781482232424
  • Weight: 742g
  • Dimensions: 156 x 234mm
  • Publication Date: 13 Oct 2014
  • Publisher: Taylor & Francis Inc
  • Publication City/Country: US
  • Product Form: Hardback
  • Language: English
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During the last 30 years, knowledge of the essential role that pyrrole structures play in the chemistry of living organisms, drug design, and the development of advanced materials has increased. Correspondingly, research on the diverse issues of synthetic, theoretical, and applied chemistry has snowballed. Devoted to the latest achievements of this field, Chemistry of Pyrroles covers the discovery and development of a novel, facile, and highly effective method for the construction of the pyrrole ring from ketones (ketoximes) and acetylene in superbase catalytic systems (Trofimov reaction). It provides cutting-edge details on the preparation of valuable but previously inaccessible pyrrole compounds. It includes approximately 1,000 structures of novel pyrrole compounds, their yields, and physical-chemical characteristics.

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.

Boris A. Trofimov, Al'bina I. Mikhaleva, Elena Yu Schmidt, Lyubov N. Sobenina

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