Synthesis and biological activity of N- and O-acyl derivatives of 2,6-diphenyl-4-hydroxypiperidines and tetrahydropyridines

Soldatenkov A.T. ¹ , Levov A.N. ¹ , Mobio I.G. ¹ , Polyakova E.V. ¹ , Kutyakov S.V. ¹ , An' L.T. ¹ , Komarova A.I. ¹ , Polyanskii K.B. ¹ , Andreeva E.I.² , Minaev L.I.²

Pharmaceutical Chemistry Journal

10

Английский

526-528

Опубликовано

Внешняя ссылка

10.1023/B:PHAC.0000014856.37517.20

37

2003

• ¹ Russian Inst. of Peoples Friendship, Moscow, Russian Federation
• ² Inst. for Chem. Means Plant Protect., Moscow, Russian Federation

2,3,6 triphenyl 1 phenylcarbamoyl 4 oxopiperidine; 2,3,6 triphenyl 1 phenylcarbamoyl 4 phenylcarbamoxylhydroxypiperidine; 4 benzoylperoxy 4 hydroxy 2,3,6 triphenylpiperidine; acyl 4 acyloxy 3,5 dimethyl 2,6 diphenyl 1,2,3,6 tetrahydropyridine derivative; acyloxy 2,3,6 triphenylpiperidine derivative; antibiotic agent; antifungal agent; antiinfective agent; unclassified drug; antibacterial activity; antifungal activity; article; Baeyer Villiger reaction; controlled study; drug structure; drug synthesis; Fusarium moniliforme; Hyphomycetes; nonhuman; physical chemistry; proton nuclear magnetic resonance; structure analysis; Xanthomonas malvacearum

19.10.2018

19.10.2018

https://repository.rudn.ru/ru/records/article/record/34/