| Literature DB >> 27929178 |
Lilya U Dzhemileva1, Vladimir A D'yakonov2, Aleksey A Makarov2, Evgeny N Andreev2, Milyausha M Yunusbaeva2, Usein M Dzhemilev2.
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.Entities:
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Year: 2017 PMID: 27929178 DOI: 10.1039/c6ob02346k
Source DB: PubMed Journal: Org Biomol Chem ISSN: 1477-0520 Impact factor: 3.876