Results 11 to 20 of about 1,058 (166)
Pd(II)/PIDA-Enabled Migratory Triple Functionalization of Terminal Alkenes via a 1,2-C/Pd(IV) Dyotropic Rearrangement. [PDF]
Pd‐catalyzed reaction of homoallylic amides with phenyliodine(III) diacetate (PIDA) under Pd(II) catalysis delivers 6‐acetoxylated 5,6‐dihydro‐4H‐1,3‐oxazines through the formation of one C─C and two C─O bonds. Abstract We report a Pd(II)‐catalyzed migratory triple functionalization of terminal alkenes.
Liu CX, Wang Q, Zhu J.
europepmc +3 more sources
Constitutive activation of NF-κB is associated with proinflammatory diseases and suppression of the NF-κB signaling pathway has been considered as an effective therapeutic strategy in the treatment of various cancers including hepatocellular carcinoma ...
Chaithanya Somu +13 more
doaj +1 more source
Cyclization of hydrazones derived from 2-acetyl-1-naphthol and 1-acetyl-2-naphthol with triphosgene gave naphtho[1,2-e]-1,3-oxazines, naphtho[2,1-e]-1,3-oxazines or their spiro dimers depending on the molar ratio of triphosgene used for the cyclization.
Hamad Zaid Alkhathlan +5 more
doaj +1 more source
A series of 2-aryl/alkyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazines (S 1 –S 11 ) were synthesized with an eco-friendly and recoverable nanocatalyst (GO-Fe3O4–Ti(IV)) as an efficient magnetic composite. The new nanocatalyst was characterized by FT-IR, XRD
Soghra Khabnadideh +8 more
doaj +1 more source
Synthesis and characterization of novel 1,2-oxazine-based small molecules that targets acetylcholinesterase [PDF]
Thirteen 2-oxazine-based small molecules were synthesized targeting 5-lipoxygenase (LOX), and acetylcholinesterase (AChE). The test revealed that the newly synthesized compounds had potent inhibition towards both 5-LOX and AChE in lower micro molar ...
Basappa, . +6 more
core +1 more source
The [4+2] cycloaddition of donor-acceptor cyclobutanes and nitrosoarenes. [PDF]
The Yb(OTf)3 catalyzed [4+2] cycloaddition between donor-acceptor cyclobutanes and nitrosoarenes is disclosed. This method facilitates the synthesis of tetrahydro-1,2-oxazines in good to excellent yields as single diastereomers. Except for a few electron-
Pagenkopf, Brian L +3 more
core +4 more sources
an Experimental and Computational Study [PDF]
To gain a deeper understanding of the formation of the synthetically important 3,6‐dihydro‐2H‐1,2‐oxazines, the 6‐endo‐trig cyclization of allenyl‐substituted hydroxylamines was experimentally investigated in detail employing a model compound.
Jasiński, Marcin +3 more
core +1 more source
Synthesis of New 1,3-Disubstituted-2,3-dihydro-1H-naphth[1,2e][1,3]oxazines
1,3-Disubstituted-2,3-dihydro-1H-naphth[1,2-e][1,3]oxazines were prepared through the ring-closurereactions of the aminobenzylnaphthols with substituted aryl-andheteroarylaldehydes.
Adem Köycü, Emel Pelit, Zuhal Turgut
doaj +1 more source
In this paper, a magnetic nanocatalyst of Fe3O4@SiO2-ZnCl2 has been used which enhances the synthesis of benzimidazoles, coumarins, benzoxazines and dihydropyrimidinones. To begin with, 2-substituted benzimidazoles have been synthesized in proper to high
Saba Rahimi, Ebrahim Soleimani
doaj +1 more source
Synthesis and characterization of novel oxazines and demonstration that they specifically target cyclooxygenase 2 [PDF]
In the present study, we used solution combustion synthesis-bismuth oxide (Bi2O3) as catalyst for the simple and efficient synthesis of 1,2-oxazine based derivatives of 6-fluoro-3-(piperidin-4-yl)benzo[d]isoxazoles, 1-arylpiperazine and carbazoles.
Baburajeev, C.P. +13 more
core +1 more source

