Synthesis of 4-methoxy-2-thiomorpholin-4-ylmethyl-1-phenol
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چکیده
منابع مشابه
Molecular Docking of 4-Tert-buthyl-bis-(2,6-thiomorpholin-4-ylmethyl)-1-phenol (LQM319) on Fas Receptor (CD95)
The balance between cell proliferation and cell growth characterizes tissue homeostasis on one side and cell death on the other side. Fas receptor-mediated apoptosis is a control mechanism for tissue homeostasis, and avoiding this death pathway predisposes to many human diseases, including cancer. Current therapies for this disease are invasive and do not have the desired effect in the control ...
متن کاملSynthesis, Characterization and Electrochemical Behaviour of 4-(4-Nitrophenyl-Azo)-2-(2-Methoxy Phenimino)-Phenol and Its Ni(II), Cu(II), Co(II) and Fe(III) Complexes
4(4-Nitrophenyl-zao)-2-(2-Methoxy phenimino)-phenol and its coordination compounds with Ni(II), Cu(II), Co(II) and Fe(III) have been synthesized and characterized by elemental analyses, FT-IR, Far-IR, Near IR, UV-Vis, mass spectrometry and molar conductivity and their electrochemical behaviours are reported.
متن کاملSYNTHESIS OF 8-HYDROXY-6-METHOXY- 3-UNDECYLISOCOUMARIN AND 2-HY DROXY - 4-METHOXY-6-(2-OXOTRIDECYL) BENZOIC ACID
Straightforward conversion of (+)-6,8-dimethoxy-3,4-dihydro-3- undecylisocoumarin (3) to the title isocoumarin was carried out. Hydrolytic ring opening of (3) afforded the hydroxy acid (4) which was immediately oxidized to keto acid (5) using chromic acid, Cyclodehydration of (5) afforded the 6,8- dimethoxy-3-undecylisocoumarin (6) which on selective demethylation of 8- methoxy group furni...
متن کاملsynthesis, characterization and electrochemical behaviour of 4-(4-nitrophenyl-azo)-2-(2-methoxy phenimino)-phenol and its ni(ii), cu(ii), co(ii) and fe(iii) complexes
4(4-nitrophenyl-zao)-2-(2-methoxy phenimino)-phenol and its coordination compounds with ni(ii), cu(ii), co(ii) and fe(iii) have been synthesized and characterized by elemental analyses, ft-ir, far-ir, near ir, uv-vis, mass spectrometry and molar conductivity and their electrochemical behaviours are reported.
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A series of (5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl derivatives 6a–6e have been synthesized and screened for in vitro anti-leishmanial activity against the promastigote form of L. major. The structure of Schiff bases were confirmed by 1H NMR, IR. Screening results indicate that all of the designed and synthesized final compounds (6a-6e) significantly reduced the viability of promastigotes ...
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ژورنال
عنوان ژورنال: Molbank
سال: 2007
ISSN: 1422-8599
DOI: 10.3390/m547