Abstract
In a novel disconnection of isoquinoline ring synthesis at the C7C8/C4aC8a bonds, these bonds can be formed by a [4+2] cycloaddition between thiophene S,S-dioxide and alkynes. With a subsequent CH arylation of the resulting hexaarylisoquinoline at the C3 position, the synthesis of a fully substituted isoquinoline has been achieved.
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Asako, T., Suzuki, S., Itami, K., Muto, K., & Yamaguchi, J. (2018). Synthesis of a heptaarylisoquinoline: Unusual disconnection for constructing isoquinoline frameworks. Chemistry Letters, 47(8), 968–970. https://doi.org/10.1246/cl.180429
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