2012
DOI: 10.1016/j.dyepig.2011.05.026
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One pot synthesis of aryl substituted aurones

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Cited by 21 publications
(16 citation statements)
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“…For the preparation of the title compound, see: Li et al (2011). For applications of indanone derivatives, see: Borge et al (2010); Cai et al (2005); Cui et al (2009); Fu & Wang (2008); Li et al (2009); Sousa et al (2011); Tang et al (2011). For related structures, see: Ali et al (2010a,b,c,d); Chen et al (2011a,b).…”
Section: Related Literaturementioning
confidence: 99%
See 1 more Smart Citation
“…For the preparation of the title compound, see: Li et al (2011). For applications of indanone derivatives, see: Borge et al (2010); Cai et al (2005); Cui et al (2009); Fu & Wang (2008); Li et al (2009); Sousa et al (2011); Tang et al (2011). For related structures, see: Ali et al (2010a,b,c,d); Chen et al (2011a,b).…”
Section: Related Literaturementioning
confidence: 99%
“…Indanone and its derivatives are some of the most widely used organic compounds (Tang et al, 2011). They are used as dyes and pigments (Cui et al, 2009;Li et al, 2009), intermediates in organic synthesis (Fu & Wang, 2008;Borge et al, 2010) and exhibit a wide variety of biological activities (Sousa et al, 2011). In addition, 1-indanones were important precursors in the regiospecific synthesis of 2-fluoro-1-naphthols (Cai et al, 2005).…”
Section: S1 Commentmentioning
confidence: 99%
“…18 Thus we achieved our first aim of reacting the diaryldiazomethanes 2a-c with compounds 3a-c to access the spiropyrazolinic skeleton 4a-i, but, the unexpected products 5a-i were obtained. Structures were assigned on the basis of their spectral data and are new pyrazoles (Scheme 1).…”
Section: Resultsmentioning
confidence: 99%
“…In the second part of our work, we were prompted to investigate the reactivity of the ( Z )‐2‐arylidene‐benzofuran‐3(2H)‐ones 6a , 6b , 6c , 6d , prepared according to the literature procedure , with 2‐diazopropane 2 . Indeed and owing to the fact that the reactions of ( Z )‐2‐arylidene‐benzofuran‐3(2 H )‐ones 6a , 6b , 6c , 6d with diazoalkanes have been well studied over the last few years , the treatment of compounds 6a , 6b , 6c , 6d with an excess of 2 at 0°C in dry dichloromethane afforded the spirocyclopropane 7a , 7b , 7c , 7d (Table ).…”
Section: Resultsmentioning
confidence: 99%