This paper is concerned with intramolecular radical additions to quinolines. Radical additions to C-2, C-3 and C-4 of a quinoline have all been shown to proceed under neutral conditions. In each case formation of heteroaromatic products, rather than dihydroquinolines, was observed (implicating the so called oxidative tin hydride pathway)
The isomerization of the primary trans-addition products formed in the hydrostannation of ethynes ha...
The work described in this thesis concerns the intramolecular addition of an aryl radical to an aren...
Organic chemists have began to use intramolecular radical addition reactions i.e. radical cyclizatio...
The paper is concerned with intramolecular radical additions to quinolines. Radical additions to C-2...
This thesis is concerned with the development of intramolecular radical additions onto nitrogen cont...
Different synthetic paths that produce the reduced quinoline cycle are discussed: among them intramo...
A new general reaction of wide synthetic interest, involving homolytic 뫉aminoalkylation of quinoxa...
Tandem radical cyclizations of suitably substituted N-aryl thiocarbamates, thioamides, and thioureas...
3,4-Dihydroquinolin-2-ones are of great importance in the areas of pharmaceuticals. However, the dir...
The reaction of 4-methoxyphenylisonitrile with phenylacetylene and AIBN produces a novel cyclopenta-...
The 2-(2-isocyanatophenyl)ethyl radical was generated from the corresponding bromide with tributylti...
Summarization: Heating the title compounds 1 at reflux in acetic anhydride yields quinoxalines 3 and...
iv, 194 leaves : ill.Thesis (Ph.D.)--University of Adelaide, Dept. of Organic Chemistry, 197
The effect of substituents on the value of the oxidation potential of quinones is reviewed and attem...
Studies in Quinoline Compounds. Part II. Some Derivatives of 4-Phenyl-2-methylquinoline
The isomerization of the primary trans-addition products formed in the hydrostannation of ethynes ha...
The work described in this thesis concerns the intramolecular addition of an aryl radical to an aren...
Organic chemists have began to use intramolecular radical addition reactions i.e. radical cyclizatio...
The paper is concerned with intramolecular radical additions to quinolines. Radical additions to C-2...
This thesis is concerned with the development of intramolecular radical additions onto nitrogen cont...
Different synthetic paths that produce the reduced quinoline cycle are discussed: among them intramo...
A new general reaction of wide synthetic interest, involving homolytic 뫉aminoalkylation of quinoxa...
Tandem radical cyclizations of suitably substituted N-aryl thiocarbamates, thioamides, and thioureas...
3,4-Dihydroquinolin-2-ones are of great importance in the areas of pharmaceuticals. However, the dir...
The reaction of 4-methoxyphenylisonitrile with phenylacetylene and AIBN produces a novel cyclopenta-...
The 2-(2-isocyanatophenyl)ethyl radical was generated from the corresponding bromide with tributylti...
Summarization: Heating the title compounds 1 at reflux in acetic anhydride yields quinoxalines 3 and...
iv, 194 leaves : ill.Thesis (Ph.D.)--University of Adelaide, Dept. of Organic Chemistry, 197
The effect of substituents on the value of the oxidation potential of quinones is reviewed and attem...
Studies in Quinoline Compounds. Part II. Some Derivatives of 4-Phenyl-2-methylquinoline
The isomerization of the primary trans-addition products formed in the hydrostannation of ethynes ha...
The work described in this thesis concerns the intramolecular addition of an aryl radical to an aren...
Organic chemists have began to use intramolecular radical addition reactions i.e. radical cyclizatio...
DOI
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