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- W2962183882 endingPage "2551" @default.
- W2962183882 startingPage "2551" @default.
- W2962183882 abstract "Disubstituted pyrenes at the non-K region by the same or different (hetero)aryl groups have proven to be an increasingly interesting area of research for scientists over the last decade due to their optical and photophysical properties. However, in this area, there is no systematization of the structures and synthesis methods nor their limitations. In this review, all approaches to the synthesis of these compounds, starting from the commercially available pyrene are described. Herein, the ways of obtaining of disubstituted intermediates based on bromination and acylation reaction are presented. This is crucial in the determination of the possibility of further functionalization by using coupling, cycloaddition, condensation, etc. reactions. Moreover, the application of disubstituted pyrenes in the synthesis of 1,3,6,8-tetrasubstituted was also reviewed. This review describes the directions of research on chemistry of disubstituted pyrenes." @default.
- W2962183882 created "2019-07-23" @default.
- W2962183882 creator A5011754806 @default.
- W2962183882 date "2019-07-12" @default.
- W2962183882 modified "2023-09-30" @default.
- W2962183882 title "Non-K Region Disubstituted Pyrenes (1,3-, 1,6- and 1,8-) by (Hetero)Aryl Groups—Review" @default.
- W2962183882 cites W1983477441 @default.
- W2962183882 cites W1984737964 @default.
- W2962183882 cites W1985499564 @default.
- W2962183882 cites W1991334941 @default.
- W2962183882 cites W1993699303 @default.
- W2962183882 cites W1994189612 @default.
- W2962183882 cites W1995978437 @default.
- W2962183882 cites W1996825457 @default.
- W2962183882 cites W1998050972 @default.
- W2962183882 cites W1998229348 @default.
- W2962183882 cites W2004604391 @default.
- W2962183882 cites W2010425051 @default.
- W2962183882 cites W2014590376 @default.
- W2962183882 cites W2024071116 @default.
- W2962183882 cites W2028356101 @default.
- W2962183882 cites W2031405847 @default.
- W2962183882 cites W2032043823 @default.
- W2962183882 cites W2038807342 @default.
- W2962183882 cites W2045398617 @default.
- W2962183882 cites W2046507741 @default.
- W2962183882 cites W2048200773 @default.
- W2962183882 cites W2049895990 @default.
- W2962183882 cites W2058905706 @default.
- W2962183882 cites W2066529899 @default.
- W2962183882 cites W2077458517 @default.
- W2962183882 cites W2083100756 @default.
- W2962183882 cites W2089069310 @default.
- W2962183882 cites W2089716154 @default.
- W2962183882 cites W2101405958 @default.
- W2962183882 cites W2116705354 @default.
- W2962183882 cites W2142382965 @default.
- W2962183882 cites W2156975826 @default.
- W2962183882 cites W2179889862 @default.
- W2962183882 cites W2229155765 @default.
- W2962183882 cites W2238652713 @default.
- W2962183882 cites W2297383157 @default.
- W2962183882 cites W2297929886 @default.
- W2962183882 cites W2305436912 @default.
- W2962183882 cites W2317725583 @default.
- W2962183882 cites W2318746189 @default.
- W2962183882 cites W2321736468 @default.
- W2962183882 cites W2327016028 @default.
- W2962183882 cites W2342955786 @default.
- W2962183882 cites W2417816129 @default.
- W2962183882 cites W2444164766 @default.
- W2962183882 cites W2462000460 @default.
- W2962183882 cites W2467361930 @default.
- W2962183882 cites W2470842539 @default.
- W2962183882 cites W2485049902 @default.
- W2962183882 cites W2488575066 @default.
- W2962183882 cites W2524479813 @default.
- W2962183882 cites W2578712045 @default.
- W2962183882 cites W2589596966 @default.
- W2962183882 cites W2599443973 @default.
- W2962183882 cites W2620336470 @default.
- W2962183882 cites W2751841144 @default.
- W2962183882 cites W2754446902 @default.
- W2962183882 cites W2760032577 @default.
- W2962183882 cites W2760287994 @default.
- W2962183882 cites W2766307484 @default.
- W2962183882 cites W2766481276 @default.
- W2962183882 cites W2767107388 @default.
- W2962183882 cites W2769653216 @default.
- W2962183882 cites W2772633985 @default.
- W2962183882 cites W2787609692 @default.
- W2962183882 cites W2789941039 @default.
- W2962183882 cites W2790388343 @default.
- W2962183882 cites W2803345583 @default.
- W2962183882 cites W2809859914 @default.
- W2962183882 cites W2885234522 @default.
- W2962183882 cites W2899553166 @default.
- W2962183882 cites W2911614108 @default.
- W2962183882 cites W2914359006 @default.
- W2962183882 cites W2932709592 @default.
- W2962183882 cites W2941046847 @default.
- W2962183882 cites W2949155749 @default.
- W2962183882 cites W2951667891 @default.
- W2962183882 cites W2953164945 @default.
- W2962183882 cites W2896185405 @default.
- W2962183882 doi "https://doi.org/10.3390/molecules24142551" @default.
- W2962183882 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6680588" @default.
- W2962183882 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31336967" @default.
- W2962183882 hasPublicationYear "2019" @default.
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