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The following term was not found in PubMed: 5-Pentafluorobenzene
Page 1
[1,5]-Hydride Shift Triggered N-Dealkylative Cyclization into 2-Oxo-1,2,3,4-tetrahydroquinoline-3-carboxylates via Boronate Complexes.
Zaitseva ER, Ivanov DS, Smirnov AY, Mikhaylov AA, Baleeva NS, Baranov MS. Zaitseva ER, et al. Molecules. 2022 Aug 18;27(16):5270. doi: 10.3390/molecules27165270. Molecules. 2022. PMID: 36014513 Free PMC article.
A new simple one-pot two-step protocol for the synthesis of 2-oxo-1,2,3,4-tetrahydroquinoline-3-carboxylate from 2-(2-(benzylamino)benzylidene)malonate under the action of BF3.Et2O was developed. ...
A new simple one-pot two-step protocol for the synthesis of 2-oxo-1,2,3,4-tetrahydroquinoline-3-carboxylate from …
From ferrocene to 1,2,3,4,5-pentafluoroferrocene: halogen effect on the properties of metallocene.
Erb W, Richy N, Hurvois JP, Low PJ, Mongin F. Erb W, et al. Dalton Trans. 2021 Nov 30;50(46):16933-16938. doi: 10.1039/d1dt03430h. Dalton Trans. 2021. PMID: 34779458 Free article.
The sequentially fluorinated ferrocenes (1-, 1,2-di, 1,2,3-tri, 1,2,3,4-tetra and 1,2,3,4,5-pentafluoroferrocene) have been synthesized from ferrocene. ...
The sequentially fluorinated ferrocenes (1-, 1,2-di, 1,2,3-tri, 1,2,3,4-tetra and 1,2,3, …
Dithiadiazole derivative 3-(4-nitrophenyl)-5-phenyl-3H-1,2,3,4-dithiadiazole-2-oxide - Novel modulator of store-operated calcium entry.
Grekhnev DA, Novikova IV, Krisanova AV, Yuskovets VN, Chernov NM, Yakovlev IP, Kaznacheyeva EV, Vigont VA. Grekhnev DA, et al. Biochem Biophys Res Commun. 2022 Oct 20;626:38-43. doi: 10.1016/j.bbrc.2022.08.001. Epub 2022 Aug 5. Biochem Biophys Res Commun. 2022. PMID: 35981420
Using calcium imaging and the patch-clamp technique we found that dithiadiazole derivative3-(4-nitrophenyl)-5-phenyl-3H-1,2,3,4-dithiadiazole-2-oxidehad a strong inhibitory effect on store-operated calcium entry at the micromolar concentration in HEK29 …
Using calcium imaging and the patch-clamp technique we found that dithiadiazole derivative3-(4-nitrophenyl)-5-phenyl-3H-1,2, …
Ring Enlargement of N-Phosphanyl-1,2,3,4-tetrahydroquinazolines.
Marchenko A, Koidan G, Hurieva AN, Shishkina S, Rusanov E, Kostyuk A. Marchenko A, et al. J Org Chem. 2020 Nov 20;85(22):14467-14472. doi: 10.1021/acs.joc.0c00750. Epub 2020 Sep 4. J Org Chem. 2020. PMID: 32830971
We found that 1-phosphanyl-1,2,3,4-tetrahydroquinazolines undergo ring enlargement. Their treatment with trifluoroacetic or hydrochloric acid afforded diazaphosphepinium salts. Deprotonation of these salts gave the corresponding neutral diazaphosphepin …
We found that 1-phosphanyl-1,2,3,4-tetrahydroquinazolines undergo ring enlargement. Their treatment with trifluo …
(S)-Methyl 2-[(3R,4R)-2-benzyl-3-(2-fur-yl)-1-oxo-1,2,3,4-tetra-hydro-isoquinoline-4-carboxamido]-3-(1H-indol-3-yl)propanoate.
Baktır Z, Akkurt M, Kandinska MI, Bogdanov MG, Büyükgüngör O. Baktır Z, et al. Acta Crystallogr Sect E Struct Rep Online. 2009 Jun 6;65(Pt 7):o1461-2. doi: 10.1107/S160053680902025X. Acta Crystallogr Sect E Struct Rep Online. 2009. PMID: 21582765 Free PMC article.
The title compound, C(33)H(29)N(3)O(5), was synthesized by the reaction of racemic trans-2-benzyl-3-(2-fur-yl)-1-oxo-1,2,3,4-tetra-hydro-isoquinoline-4-carboxylic acid, l-tryptophan methyl ester and diisopropylcarbodiimide in dry dichloro-methane. The …
The title compound, C(33)H(29)N(3)O(5), was synthesized by the reaction of racemic trans-2-benzyl-3-(2-fur-yl)-1-oxo-1,2,3 …
The Journey of 1-Keto-1,2,3,4-Tetrahydrocarbazole Based Fluorophores: From Inception to Implementation.
Mitra AK. Mitra AK. J Fluoresc. 2022 Nov;32(6):2023-2052. doi: 10.1007/s10895-022-03004-2. Epub 2022 Jul 13. J Fluoresc. 2022. PMID: 35829843 Review.
It is due to the diverse and versatile biological properties of carbazole derivatives that they are of immense interest to the research community. 1-keto-1,2,3,4-tetrahydrocarbazoles are important synthetic intermediates to obtain carbazole derivatives …
It is due to the diverse and versatile biological properties of carbazole derivatives that they are of immense interest to the research comm …
Poly[hexa-aqua-(mu9-cyclo-hexane-1,2,3,4,5,6-hexa-carboxyl-ato)trimanganese(II)].
Sun W, Zang H, Quan C. Sun W, et al. Acta Crystallogr Sect E Struct Rep Online. 2013 Jun 15;69(Pt 7):m384. doi: 10.1107/S1600536813015626. eCollection 2013. Acta Crystallogr Sect E Struct Rep Online. 2013. PMID: 24046563 Free PMC article.
The asymmetric unit of the title compound, [Mn3(C12H6O12)(H2O)6] n , comprises one Mn(II) ion, one third of a cyclo-hexane-1,2,3,4,5,6-hexa-carboxyl-ate anion and two aqua ligands. The anion is completed by application of a -3 axis. ...The six carboxyl …
The asymmetric unit of the title compound, [Mn3(C12H6O12)(H2O)6] n , comprises one Mn(II) ion, one third of a cyclo-hexane-1,2 …
Improved Syntheses of Halogenated Benzene-1,2,3,4-Tetracarboxylic Diimides.
Zou B, Stellmach KA, Luo SM, Gebresilassie FL, Jung H, Zhang CK, Bass AD, Janzen DE, Cao DD. Zou B, et al. J Org Chem. 2022 Nov 4;87(21):13605-13614. doi: 10.1021/acs.joc.2c01241. Epub 2022 Oct 5. J Org Chem. 2022. PMID: 36198127
The preparation of halogenated benzene-1,2,3,4-tetracarboxylic diimide derivatives is challenging because of the possibility of competitive incorrect cyclizations and S(N)Ar reactivity. Here, we demonstrate that bypassing traditional cyclic anhydrides …
The preparation of halogenated benzene-1,2,3,4-tetracarboxylic diimide derivatives is challenging because of the …
1,2,3,4-Tetrahydroisoquinoline Derivatives as a Novel Deoxyribonuclease I Inhibitors.
Gajić M, Ilić BS, Bondžić BP, Džambaski Z, Kojić VV, Jakimov DS, Kocić G, Šmelcerović A. Gajić M, et al. Chem Biodivers. 2021 Aug;18(8):e2100261. doi: 10.1002/cbdv.202100261. Epub 2021 Jul 13. Chem Biodivers. 2021. PMID: 34170076
Herein we report an assessment of 24 1,2,3,4-tetrahydroisoquinoline derivatives for potential DNase I (deoxyribonuclease I) inhibitory properties in vitro. Four of them inhibited DNase I with IC(50) values below 200 muM. The most potent was 1-(6,7-dime …
Herein we report an assessment of 24 1,2,3,4-tetrahydroisoquinoline derivatives for potential DNase I (deoxyribo …
In vitro anti-hepatocellular carcinogenesis of 1,2,3,4,6-Penta-O-galloyl-beta-D-glucose.
Jiang YH, Bi JH, Wu MR, Ye SJ, Hu L, Li LJ, Yi Y, Wang HX, Wang LM. Jiang YH, et al. Food Nutr Res. 2023 Mar 27;67. doi: 10.29219/fnr.v67.9244. eCollection 2023. Food Nutr Res. 2023. PMID: 37050924 Free PMC article.
BACKGROUND: 1,2,3,4,6-Penta-O-galloyl-beta-D-glucose (beta-PGG) is a polyphenol ellagic compound with a variety of pharmacological effects and has an inhibitory effect on lots of cancers. OBJECTIVE: To explore the antitumor effects and mechanism of …
BACKGROUND: 1,2,3,4,6-Penta-O-galloyl-beta-D-glucose (beta-PGG) is a polyphenol ellagic compound with a variety …
19,800 results
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