Short synthesis of a new cyclopentene-1,3-dione derivative isolated from Piper carniconnectivum

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Abstract

The total synthesis of cyclopentene-1,3-dione (1), a new natural cyclopentenedione derivative isolated from the roots of Piper carniconnectivum, is described in 8 steps and 11% overall yield from 2-acetylfuran, giving a 57:43 mixture of the two possible geometric isomers 1a and1b. ©2005 Sociedade Brasileira de Química.

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APA

Dias, L. C., Shimokomaki, S. B., & Shiota, R. T. (2005). Short synthesis of a new cyclopentene-1,3-dione derivative isolated from Piper carniconnectivum. Journal of the Brazilian Chemical Society, 16(3 A), 482–489. https://doi.org/10.1590/S0103-50532005000300024

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