Oxime ethers as versatile precursors in organic synthesis: a review

Z Mirjafary, M Abdoli, H Saeidian, S Boroon… - RSC …, 2015 - pubs.rsc.org
Oxime ethers as versatile precursors in organic synthesis: a review - RSC Advances (RSC
Publishing) DOI:10.1039/C5RA15299B Royal Society of Chemistry View PDF VersionPrevious …

Review of the synthesis of acyclic and cyclic oxime ethers

Z Mirjafary, M Abdoli, H Saeidian, A Kakanejadifard… - RSC …, 2016 - pubs.rsc.org
Oxime ethers have attracted much attention due to their potential biological activities and
wide variety of synthetic applications. Developing more efficient methods for the synthesis of …

Oxime ethers as useful synthons in the synthesis of a number of key medicinal heteroaromatic compounds

E Vessally, M Abdoli - Journal of the Iranian Chemical Society, 2016 - Springer
Heteroaromatic systems are not only prevalent in a wide variety of important classes of
natural products and synthetic pharmaceuticals but are also used as a building block in …

Nitrile N-oxides and nitrile imines as new fuels for the discovery of novel isocyanide-based multicomponent reactions

M Giustiniano, E Novellino, GC Tron - Synthesis, 2016 - thieme-connect.com
With this short review we would like to describe our work on isocyanide-mediated
multicomponent reactions using the 1, 3-dipolar species nitrile N-oxides and nitrile imines as …

Synthesis of indolo [2, 3-c] quinolines from 3-arylindole-2-ketoximes

TD Wahyuningsih, N Kumar, DSC Black - Tetrahedron, 2007 - Elsevier
Synthesis of indolo[2,3-c]quinolines from 3-arylindole-2-ketoximes - ScienceDirect Skip to
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[PDF][PDF] Synthesis, Reactivity and Biological Properties of Methoxy-Activated Indoles

IF Sengul, M Bingul, H Kandemir, N Kumar… - Targets in Heterocyclic …, 2021 - soc.chim.it
Indoles continue to play a central role in the development of new structures of chemical and
biological interest. They are the source of numerous biologically active natural products by …

Rapid synthesis of substituted pyrrolines and pyrrolidines by nucleophilic ring closure at activated oximes

N Chandan, AL Thompson, MG Moloney - Organic & Biomolecular …, 2012 - pubs.rsc.org
Substituted pyrrolines are available by ring closure initiated by direct nucleophilic attack of
stabilized enolates at the nitrogen of oximes activated with a leaving group, in a process …

Synthesis of macrocyclic tetraindolyls via oxidative coupling reactions

R Chen, M Bhadbhade, N Kumar, DSC Black - Tetrahedron Letters, 2012 - Elsevier
Synthesis of macrocyclic tetraindolyls via oxidative coupling reactions - ScienceDirect Skip
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Solution-Phase Parallel Synthesis of Aryloxyimino Amides via a Novel Multicomponent Reaction among Aromatic (Z)-Chlorooximes, Isocyanides, and Electron …

V Mercalli, M Giustiniano, E Del Grosso… - ACS Combinatorial …, 2014 - ACS Publications
A library of 41 aryloxyimino amides was prepared via solution phase parallel synthesis by
extending the multicomponent reaction of (Z)-chlorooximes and isocyanides to the use of …

Synthetic strategies for aspartic and glutamic acid-proline chimeras: A review

A Stefanucci, R Costante, S Carradori… - Mini-Reviews in …, 2015 - ingentaconnect.com
Proline chimeras are conformationally rigid amino acid analogues. Their application in
medicinal chemistry for the synthesis of peptidomimetics is a well-known approach. Of …