首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >An expedient synthesis of N,N-dialkylamino-dihydroxanthene-pyrylium conjugated near-infrared fluorescent dyes
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An expedient synthesis of N,N-dialkylamino-dihydroxanthene-pyrylium conjugated near-infrared fluorescent dyes

机译:N,N-二烷基氨基-二氢氧杂蒽-吡啶共轭近红外荧光染料的简便合成

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摘要

An expedient synthesis of amino-(nor)dihydroxanthene-based fluorophores is reported, proceeding in two steps from commercially available salicylic aldehydes. The synthesis relies on the one-pot construction of the (nor)dihydroxanthene scaffolds through an oxa-Michael/retro-Michael/vinylogous aldol/dehydration cascade sequence. Further extension of the pi-conjugated systems through a condensation reaction with a 2,4,6-trisubstituted pyrylium salt led to a novel class of near-infrared (NIR) fluorescent dyes with absorption/emission maxima in polar media in the ranges of 705-778 and 785-828 nm, respectively. (C) 2015 Elsevier Ltd. All rights reserved.
机译:据报道,从商业上可得的水杨醛分两步进行氨基-(正)二氢氧杂蒽基荧光团的合成。合成依赖于通过氧杂-迈克尔/复古迈克尔/葡萄酒醛醇/脱水级联序列的(去)二氢黄嘌呤骨架的一锅构建。通过与2,4,6-三取代的吡啶鎓盐的缩合反应进一步扩展π共轭体系,导致了一类新型的近红外(NIR)荧光染料,在极性介质中的吸收/发射最大值在705范围内-778和785-828 nm。 (C)2015 Elsevier Ltd.保留所有权利。

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