Abstract
The communication reports a new stereoselective method for the synthesis of a natural acetylenic alcohol, lembehyne B. The key stage of the process uses new cross-cyclomagnesiation reaction of aliphatic and oxygenated 1,2-dienes with Grignard reagents in the presence of a catalytic amount of Cp2TiCl2. A study of the cytotoxic properties of lembehyne B on tumor cell lines using flow cytometry demonstrated that this is a selective inducer of early apoptosis of the Jurkat, HL-60 and K562 cell cultures and hypodiploid (sub-G1) sub-population inducer in cell cycle studies for all cell lines used.
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CITATION STYLE
Dzhemileva, L. U., D’yakonov, V. A., Makarov, A. A., Andreev, E. N., Yunusbaeva, M. M., & Dzhemilev, U. M. (2017). The first total synthesis of the marine acetylenic alcohol, lembehyne B-a selective inducer of early apoptosis in leukemia cancer cells. Organic and Biomolecular Chemistry, 15(2), 470–476. https://doi.org/10.1039/c6ob02346k
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