CuBr 2 ‐Promoted Multicomponent Aerobic Reaction for the Synthesis of 1,2,3‐Triaroylindolizines

2019 ◽  
Vol 56 (8) ◽  
pp. 2253-2261 ◽  
Author(s):  
Jinwei Sun ◽  
Junwen Han ◽  
Yuxuan Zhang ◽  
Yun Liu
Keyword(s):  
2009 ◽  
Vol 34 (6) ◽  
pp. 677-681 ◽  
Author(s):  
Wagner José Barreto ◽  
Sonia Regina Giancoli Barreto ◽  
Waleria Pickina Silva
Keyword(s):  

1989 ◽  
Vol 67 (6) ◽  
pp. 1061-1064 ◽  
Author(s):  
H. Al-Ekabi ◽  
A. M. Draper ◽  
P. De Mayo

Three reactions: the CdS-mediated valence isomerization of hexamethyldewarbenzene to hexamethylbenzene, the cycloreversion of dianthracene, and the TiO2-mediated cis–trans isomerization of stilbene are known to be suppressed when the semiconductor excitation takes place in the absence of oxygen. The oxygen, when present, is presumed to trap the electron delaying electron-hole recombination. It has been found that CBr4 may replace oxygen and functions in a similar way. In addition, the concomitant formation of oxidation products in the TiO2-mediated aerobic reaction is avoided. The mechanism is discussed. Keywords: cadmium sulphide, carbon tetrabromide, dianthracene, heterogeneous photocatalysis, hexamethyldewarbenzene, titanium oxide.


Author(s):  
Rishabh Sehgal

Abstract: With the rapid decrease in conventional energy sources and serious issues like Global Warming and change in the climate, there is an immediate need to find sources that are renewable and will last for a long time. Hydrogen as a fuel is a good alternative given its abundance. Hydrogen production uses natural gases and electrolysis of water, thus directly or indirectly creating pollution. But this doesn’t mean that energy provided by hydrogen is clean in the utmost sense. Hence there is a need to segregate and analyze different Hydrogen production techniques. In this paper, we will briefly discuss the biological methods of Hydrogen production from biomass and applications of hydrogen. Keywords: Biological H2 production, Aerobic Reaction, Anaerobic reactions, Fuel cell.


1979 ◽  
Vol 179 (3) ◽  
pp. 649-656 ◽  
Author(s):  
C R Slack ◽  
P G Roughan ◽  
J Browse

1. [14C]Oleoyl-CoA was metabolized rapidly and essentially completely by microsomal preparations from developing safflower (Carthamus tinctorius) cotyledons, and most of the [14C]oleate was incorporated into 3-sn-phosphatidylcholine. 2. In aerobic reaction mixtures containing NADH2 the [14C]oleate in 3-sn-phosphatidylcholine was converted into [14C]linoleate without any change in the specific radioactivity of the lipid. Over a 60 min incubation period the extent of conversion of [14C]oleoyl phosphatidylcholine into [14C]linoleoyl phosphatidylcholine was generally greater than 60%. The rate of desaturation of endogenous [14C]oleoyl phosphatidylcholine labelled from [14C]oleoyl-CoA was much greater that of exogenous [14C]dioleoyl phosphatidylcholine the specific radioactivity of the oleoyl moiety of the lipid remained constant, indicating that labelled and unlabelled oleate were desaturated at the same rate. On this assumption an initial rate of desaturation of about 15 nmol of oleate desaturated/min per mumol of 3-sn-phosphatidylcholine was estimated. 4. [14C]Oleate esterified at positions 1 and 2 of both endogenous and exogenous 3-sn-phosphatidylcholine was desaturated. 5. Attempts to demonstrate the presence of an oleoyl-CoA desaturase in safflower microsomal fractions by the appearance of linoleoyl-CoA in reaction mixtures were inconclusive.


2015 ◽  
Vol 11 ◽  
pp. 1933-1943 ◽  
Author(s):  
Ya Lin Tnay ◽  
Gim Yean Ang ◽  
Shunsuke Chiba

We report herein studies on copper-catalyzed aerobic radical C–C bond cleavage of N–H ketimines. Treatment of N–H ketimines having an α-sp3 hybridized carbon under Cu-catalyzed aerobic reaction conditions resulted in a radical fragmentation with C–C bond cleavage to give the corresponding carbonitrile and carbon radical intermediate. This radical process has been applied for the construction of oxaspirocyclohexadienones as well as in the electrophilic cyanation of Grignard reagents with pivalonitrile as a CN source.


Synlett ◽  
2015 ◽  
Vol 26 (08) ◽  
pp. 1121-1123 ◽  
Author(s):  
Jing-Hua Li ◽  
Jun Yu ◽  
Shuguang Wang ◽  
Jianming Wen ◽  
Jian Wang

A novel method for conversion of N′-arylhydrazides to N′,N′-diarylhydrazides via aerobic oxidation has been achieved. The aerobic reaction was performed using CuCl2 as a catalyst in NH3·H2O–MeOH to give good yields under mild conditions. The mechanism of the reaction is also discussed.


2019 ◽  
Vol 26 (2) ◽  
pp. 450-461 ◽  
Author(s):  
Alejandra Enriquez Garcia ◽  
Farideh Jalilehvand ◽  
Pantea Niksirat

The structural differences between the aerobic reaction products of Rh2(AcO)4(1; AcO−= CH3COO−) with thiols and thiolates in non-aqueous media are probed by X-ray absorption spectroscopy. For this study, ethanethiol, dihydrolipoic acid (DHLA; a dithiol) and their sodium thiolate salts were used. Coordination of simple thiols to the axial positions of Rh2(AcO)4with Rh—SH bonds of 2.5–2.6 Å keeps the RhII—RhIIbond intact (2.41 ± 0.02 Å) but leads to a colour change from emerald green to burgundy. Time-dependent density functional theory (TD-DFT) calculations were performed to explain the observed shifts in the electronic (UV–vis) absorption spectra. The corresponding sodium thiolates, however, break up the Rh2(AcO)4framework in the presence of O2to form an oligomeric chain of triply S-bridged Rh(III) ions, each with six Rh—S (2.36 ± 0.02 Å) bonds. The RhIII...RhIIIdistance, 3.18 ± 0.02 Å, in the chain is similar to that previously found for the aerobic reaction product from aqueous solutions of Rh2(AcO)4and glutathione (H3A), {Na2[Rh2III(HA)4]·7H2O}n, in which each Rh(III) ion is surrounded by about four Rh—S (2.33 ± 0.02 Å) and about two Rh—O (2.08 ± 0.02 Å). The reaction products obtained in this study can be used to predict how dirhodium(II) tetracarboxylates would react with cysteine-rich proteins and peptides, such as metallothioneins.


2020 ◽  
Vol 40 (6) ◽  
pp. 1697
Author(s):  
Ablimit Abdukader ◽  
Rong Wang ◽  
Marhaba Mamat ◽  
Chenjiang Liu
Keyword(s):  

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