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- W4292212413 endingPage "132911" @default.
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- W4292212413 abstract "An efficient method for the synthesis of 7H-benzo[4,5]isothiazolo[3,2- b ]quinazolin-7-ones from the reaction of 2-(2-bromophenyl)quinazolin-4(3H)-one and elemental sulfur via N–S/C–S bond formation under transition-metal-free conditions is described. The reaction performed smoothly under simple conditions to give the corresponding products in good to high yields with good functional group tolerance. Moreover, the synthesized 7H-benzo[4,5]isothiazolo[3,2- b ]quinazolin-7-ones show enhanced UV–Vis light absorption ability, due to the sulfur induced extension of the intramolecular conjugation, compared to 2-phenyl-quinazolin-4(3H)-one, indicating the potential application of these molecules in the field of organic light absorbing materials." @default.
- W4292212413 created "2022-08-18" @default.
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- W4292212413 date "2022-10-01" @default.
- W4292212413 modified "2023-10-17" @default.
- W4292212413 title "Aminothiolation of 2-(2-bromophenyl)quinazolinones with elemental sulfur to access 7H-benzo[4,5]isothiazolo[3,2-b]quinazolinones through C–S/S–N bond formation under metal-free condition" @default.
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- W4292212413 doi "https://doi.org/10.1016/j.tet.2022.132911" @default.
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