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- W2897718238 abstract "A series of bent p-terphenyl-containing macrocycles have been synthesized and then regioselectively brominated, arylated, and subsequently subjected to a Scholl-based cyclodehydrogenation reaction. Shortening the alkyloxy bridging unit of these macrocycles increases the bend in the p-terphenyl unit, as well as the strain energy (SE) of the central para-phenylene ring system. For the first time, incremental increases in SE of the macrocyclic structure of this class of benzenoid compounds have been investigated in the context of π-extension to strained polycyclic aromatic hydrocarbon systems using the Scholl reaction." @default.
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- W2897718238 date "2018-10-22" @default.
- W2897718238 modified "2023-09-27" @default.
- W2897718238 title "π-Extension of Strained Benzenoid Macrocycles Using the Scholl Reaction" @default.
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- W2897718238 doi "https://doi.org/10.1021/acs.orglett.8b02979" @default.
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