1984
DOI: 10.1007/bf00505716
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Photocyclization of 1,2-diaryl- and photobicyclization of 1,2,6-triarylpyridinium cations

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Cited by 4 publications
(8 citation statements)
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“…Conversion of ( 2) into the corresponding N -aryl-2,6-bis(2-thienyl)-4-phenyl pyrydinium tetrafluoroborates 3a – c by reaction with 4-alkylanilines also followed a standard procedure, described in the literature [ 46 ]. The photocatalytic bicyclization of N -aryl-2,4,6-trisubstituted pyridinium salts has been previously described [ 47 ] and the procedure was adapted to the preparation of tetrafluoroborate salts 4a – c from the corresponding pyridinium salts 3a – c.…”
Section: Resultsmentioning
confidence: 99%
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“…Conversion of ( 2) into the corresponding N -aryl-2,6-bis(2-thienyl)-4-phenyl pyrydinium tetrafluoroborates 3a – c by reaction with 4-alkylanilines also followed a standard procedure, described in the literature [ 46 ]. The photocatalytic bicyclization of N -aryl-2,4,6-trisubstituted pyridinium salts has been previously described [ 47 ] and the procedure was adapted to the preparation of tetrafluoroborate salts 4a – c from the corresponding pyridinium salts 3a – c.…”
Section: Resultsmentioning
confidence: 99%
“…To the best of our knowledge, photocyclized pyridinium salts have never been proposed as potential n-type organic semiconductors. Their synthesis by photocyclization of readily obtained N-arylpyridinium salts has been described for more than thirty years [46,47]. More recently, some of their derivatives such as 2-phenyl-benzo [8,9]quinolizino [4,5,6,7-fed]-phenanthridinylium tetrafluoroborate (PQPBF 4 ) have been shown to form columnar π-stacked aggregates in the solid phase [48].…”
Section: Acceptormentioning
confidence: 99%
“…
Owing to the importance of pyrimidine derivatives, considerable attention has been devoted to their chemistry and biological activity. 1 In recent years, there has been increasing interest in their synthesis, and some methods allow access to a large number of multifunctionalised pyrimidine derivatives. [2][3][4][5] The current interest in selenium-containing organic compounds stems from their remarkable biological functions.
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mentioning
confidence: 99%
“…A tentative mechanism for this transformation is proposed in Scheme 2. The reaction starts with formation of aroyl isoselenocyanate 5, followed by addition of 6-amino-N,N′dimethyluracil 1 to generate 6, subsequent cyclisation of which generates 7, which is converted into 4 by elimination of water and a [1,3]-H shift.…”
mentioning
confidence: 99%
“…[1][2][3][4] Since the isolation of pyrimidine derivatives, considerable attention has been devoted to their chemistry and biological activity. 5 The current interest in seleniumcontaining organic compounds stems from their remarkable synthetic and biological functions. [6][7][8][9][10] The first synthesis of acyl isoselenocyanates, which were generated by the reaction of acyl chlorides and potassium selenocyanate, was described by Douglas.…”
mentioning
confidence: 99%