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- W2033452911 abstract "Exposure of 1a to MsCl in the presence of Et 3 N, followed by treatment with H 2 O provided anthracene and phenanthrene derivatives 4 and 5 in an (1:1) product ratio via 1,6-didehydro[10]annulene intermediate. Under the same conditions 2a gave naphthalene derivative 6 in 9% yield via ene-yne-allene intermediate. These transformation could be explained by the rapid diradicalforming cycloaromatization. 1a reacted with MsCl in the presence of Et 3 N, followed by treatment with H 2 O to give 4 and 5 in an (1:1) product ratio. Under the same conditions, 2a gave 6 in 9% yield. Both reactions proceed via diradical intermediates." @default.
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- W2033452911 date "1995-08-01" @default.
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- W2033452911 title "Cycloaromatization of 6,7-benzobicyclo[8.3.0]trideca-6,10-diene-3,8-diyne-1,5-diols via diradical intermediates" @default.
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- W2033452911 doi "https://doi.org/10.1016/0040-4039(95)01092-v" @default.
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