Abstract
Kaempferol (1), a natural product from various plants, was synthesized in which the longest linear sequence is only seven steps in overall yields of 47% from commercially available 1,3,5-trimethoxybenzene (10). The methylated kaempferols 2-5 were also prepared by use of this concise synthetic methodology. The key transformations in this synthesis involved the I2 oxidative-promoting-cyclization and DDO oxidative hydroxylation. Several strategies to achieve 1 are provided.
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Lee, Y. J., & Wu, T. D. (2001). Total synthesis of kaempferol and methylated kaempferol derivatives. Journal of the Chinese Chemical Society, 48(2), 201–206. https://doi.org/10.1002/jccs.200100033
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