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Efficient Synthesis and Antiproliferative Evaluation of New Bioactive N-, P-, and S-Heterocycles
Organophosphorus compounds are attractive and fruitful branch of chemistry that includes many tools and methods for easy research and targeted drugs formation. The reactions iso(thio)cyanates with organophosphorus reagents are studied. When N -phenyliminiovinylidenetriphenylphosphorane reacts with i...
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Published in: | Russian journal of general chemistry 2022-09, Vol.92 (9), p.1761-1774 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Organophosphorus compounds are attractive and fruitful branch of chemistry that includes many tools and methods for easy research and targeted drugs formation. The reactions iso(thio)cyanates with organophosphorus reagents are studied. When
N
-phenyliminiovinylidenetriphenylphosphorane reacts with isocyanate produces azetiidinone, dihydropyrimidinedione and oxazinone derivatives. Moreover, isothiocyante can also react with the same reagent to give theitane, thiazinanethione and dithiane derivatives. On the other side, when iso(thio)cyanate reacts with the stabilized phosphonium ylides, the new phosphorane derivatives are obtained. In addition, the reaction of hexamethyltriaminophosphine with isocyanate and isothiocyanate in dry THF give carbamimidic acid and phosphonium betaine derivatives respectively. Moreover, thirteen of the newly synthesized products were screened
in vitro
for their activity against HepG-2, HCT116, and MCF-7 human cancer cell lines. |
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ISSN: | 1070-3632 1608-3350 |
DOI: | 10.1134/S1070363222090183 |