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1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c03064
Abstract: A mild photoredox approach enabling the first one-step synthesis of thiolated 2-aminothiazoles has been reported. Notably, the incorporation of thio group on electron-rich heteroarenes such as aminothiazoles via conventional nucleophilic aromatic substitution (SNAr) presents a…
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Keywords:
selective synthesis;
photoredox promoted;
synthesis thiolated;
promoted selective ... See more keywords
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2
Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c01550
Abstract: A novel visible-light-promoted selective sulfonylation and selenylation of dienes with selenosulfonates has been developed. This technology provides mild access to a wide range of sulfonyl benzo[b]azepinones and seleno-benzo[b]azepines. Preliminary mechanistic studies suggest that the sulfonylation…
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Keywords:
sulfonylation;
light promoted;
selenylation;
selective sulfonylation ... See more keywords
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0
Published in 2017 at "ACS Omega"
DOI: 10.1021/acsomega.7b00627
Abstract: A highly efficient domino protocol has been developed for the synthesis of 6-aryl-4-(methylthio/amine-1-yl)-2-oxo-2H-pyran-3-carbonitriles and 4-aryl-2-(amine-1-yl)-5,6,7,8-tetrahydronaphthalene-1-carbonitriles from simple and readily available α-aroylketene dithioacetals, malononitrile, secondary amines, and cyclohexanone. This elegant domino process involved consecutive addition–elimination, intramolecular…
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Keywords:
selective synthesis;
domino;
promoted selective;
synthesis pyranones ... See more keywords
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Published in 2019 at "Synthesis"
DOI: 10.1055/s-0037-1610354
Abstract: The reactivity of N-thiophthalimides with silyl chalcogenides is described. Treatment of N-thiophthalimides with bis(trimethylsilyl) sulfide [(Me3Si)2S] leads to the formation of a mixture of the corresponding disulfides and trisulfides. On the other hand, N-thiophthalimides react…
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Keywords:
transformation thiophthalimides;
selective mild;
selenosilane promoted;
thiophthalimides symmetric ... See more keywords
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1
Published in 2022 at "Beilstein Journal of Organic Chemistry"
DOI: 10.3762/bjoc.18.165
Abstract: An α-cyclodextrin protected with 2,4-dichlorobenzyl groups on the primary alcohols and ordinary benzyl groups on the secondary alcohols was prepared and subjected to DIBAL (diisobutylaluminum hydride)-promoted selective debenzylation. Debenzylation proceeded by first removing two dichlorobenzyl…
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Keywords:
benzyl;
selective debenzylation;
benzyl groups;
cyclodextrin protected ... See more keywords