Tetrahedron Letters p. 5137 - 5140 (1992)
Update date:2022-09-26
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Schiesser
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Substituted 2-benzylseleno-1-(2-iodophenyl)ethanols (6) react smoothly with tris(trimethyl)silane (TTMSS) ion benzene at 80° (AIBN initiator) to give benzo[b]selenophenes (3) in 80-86% yield. Interestingly, when the parent selenide (6:R1+R
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Doi:10.1002/aoc.2968
(2013)Doi:10.1080/10426509708545546
(1997)Doi:10.1080/07328319608002379
(1996)Doi:10.1002/hlca.19670500810
(1967)Doi:10.1016/0040-4020(95)01113-7
(1996)Doi:10.1080/14786419.2020.1827399
(2020)
