2019
DOI: 10.1039/c9cc03604k
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A trisulfur radical anion (S3˙) involved sulfur insertion reaction of 1,3-enynes: sulfide sources control chemoselective synthesis of 2,3,5-trisubstituted thiophenes and 3-thienyl disulfides

Abstract: Cascade cyclization reactions of S3˙−in situ generated from S2− with 1,3-enynes for the chemoselective synthesis of 2,3,5-trisubstituted thiophenes and 3-thienyl disulfides controlled by sulfide salts are developed.

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Cited by 40 publications
(17 citation statements)
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“…Sulfur compounds are widely found in natural products, pharmaceutical molecules, and functional materials . Sulfone compounds have been utilized as indispensable building blocks in modern organic chemistry.…”
mentioning
confidence: 99%
“…Sulfur compounds are widely found in natural products, pharmaceutical molecules, and functional materials . Sulfone compounds have been utilized as indispensable building blocks in modern organic chemistry.…”
mentioning
confidence: 99%
“…Research Articles optoelectronic devices,s uch as organic light-emitting diodes (OLEDs), [18] organic field-effect transistors (OFETs), [19] organic electrochromic devices(ECDs), [20] and organic solar cells (OSCs). [21] Started with disulfides 4 and diselenide 6a,derivatizations were also carried out and the results were shown in Figure 2B (bottom). Thea rylation of 4a and 6a with aniline were achieved by free radical process to lead to compounds 9a and 9b,r espectively.…”
Section: Angewandte Chemiementioning
confidence: 99%
“…Forschungsartikel optoelectronic devices,s uch as organic light-emitting diodes (OLEDs), [18] organic field-effect transistors (OFETs), [19] organic electrochromic devices(ECDs), [20] and organic solar cells (OSCs). [21] Started with disulfides 4 and diselenide 6a,derivatizations were also carried out and the results were shown in Figure 2B (bottom). Thea rylation of 4a and 6a with aniline were achieved by free radical process to lead to compounds 9a and 9b,r espectively.…”
Section: Angewandte Chemiementioning
confidence: 99%