Abstract
The total synthesis of enantiomerically enriched (3S, 5R, 3'S, 5'R)-capsorubin (1) by aldol condensation of (1R, 4S)-1-(4-hydroxy-1,2,2-trimethyl-cyclopentyl)ethanone (2a) and crocetindial (3) is described. An alternative, short eight-step synthesis of the optically active compound 2a (ee 89%) is also reported. © 2009 Sociedade Brasileira de Química.
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Frederico, D., Constantino, M. G., & Donate, P. M. (2009). Total synthesis of (3S, 5R, 3’S, 5’R)-capsorubin. Journal of the Brazilian Chemical Society, 20(5), 888–894. https://doi.org/10.1590/S0103-50532009000500013
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