Author Topic: 2009 Reference and Translation Requests  (Read 3039 times)

java

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Re: Wanted References and Translations
« Reply #180 on: December 28, 2009, 08:32:59 PM »

The serotonin 5-HT2A receptor agonist TCB-2: a behavioral and neurophysiological analysis
Meredith A. Fox, Helen T. French, Justin L. LaPorte, Adele R. Blackler and Dennis L. Murphy
Psychopharmacology2009,Volume 205, Number 4, Epubs Ahead of Print


Abstract
Rationale  There are few reports on the high-affinity 5-HT2A agonist (4-Bromo-3,6-dimethoxybenzocyclobuten-1-yl)methylamine hydrobromide (TCB-2).

Objectives  Here we provide the first behavioral and neurophysiological profile of TCB-2 in C57BL/6J mice, with direct comparisons to the 5-HT2A/2C agonist (±)-2,5-dimethoxy-4-iodophenyl-2-aminopropane (DOI), in addition to determinations of 5-HT2A mediation via pretreatment with the selective 5-HT2A antagonist MDL 11,939.

Results  In a dose-dependent manner, TCB-2 induced head twitches, decreased food consumption in food-deprived mice, induced hypothermia, and increased corticosterone levels, with no effects on locomotor activity or anxiety-like behaviors in the open field. Similar effects were observed in side-by-side dose–response comparisons with DOI; although at the highest dose tested (5.0 mg/kg), TCB-2 induced significantly fewer head twitches, and a significantly enhanced hypothermic response, versus DOI. Pretreatment with MDL 11,939 blocked head twitches and temperature change following TCB-2 and DOI, confirming 5-HT2A mediation of these responses. Although MDL 11,939 pretreatment blocked DOI-induced suppression of feeding, MDL 11,939 had no effect on TCB-2-induced suppression of feeding. Previous studies show that 5-HT2A function is altered by changes in serotonin transporter (SERT) expression and function. In SERT knockout (?/?) mice, TCB-2-induced head twitches and hypothermia were greatly diminished compared to SERT wild-type (+/+) mice.

Conclusions  The current studies are important, as they are the first to assess the effects of TCB-2 in mice, and are among the first to report the behavioral and neurophysiological effects of this conformationally restricted phenethylamine analog compound, which has 65-fold greater effects on signaling via the phosphoinositide versus arachidonic acid pathways.[/color]



¡Prefiero morir de pie que vivir siempre arrodillado!.Emiliano ZapataIt is better to die on your feet than to live on your knees!.......

java

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Re: Wanted References and Translations
« Reply #181 on: December 29, 2009, 03:48:33 PM »
Comment by no1uno
I honestly suspect that those latest compounds, the anthrecenes, may well avoid the application of the analogue acts, they are neither structurally similar to anything that is illegal, and NOBODY would be dumb enough to represent it as having similar properties, would they?



High-Yield Synthesis of Dimethyl Carbonate from Urea and Methanol Using a Catalytic Distillation Process
Mouhua Wang, Hui Wang, Ning Zhao, Wei Wei, and Yuhan Sun
Ind. Eng. Chem. Res. 2007, 46 (9), pp 2683–2687
DOI: 10.1021/ie061101u



Abstract
Reaction equilibrium for the dimethyl carbonate (DMC) synthesis from urea and methanol was calculated based on the Benson method, and results showed that the reaction was thermodynamically unfavorable. In addition, urea methanolysis was conformed to be a consecutive reaction. Major side reactions in the DMC synthesis included the thermal decomposition of DMC and reaction between methyl carbamate (MC) and DMC, which reduced the DMC yield in the batch process. A catalytic distillation technique was proposed in this study to minimize the side reactions and unfavorable equilibrium for DMC synthesis. The DMC yield reached 60?70% in the catalytic distillation reactor over a Zn-based catalyst.


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Modeling of the Catalytic Distillation Process for the Synthesis of Dimethyl Carbonate by Urea Methanolysis Method
Feng Wang, Ning Zhao, Junping Li, Wenbo Zhao, Fukui Xiao, Wei Wei, and Yuhan Sun
Ind. Eng. Chem. Res. 2007, 46 (26), pp 8972–8979




Abstract
A nonequilibrium model of the catalytic distillation was developed for the process of DMC synthesis by a urea methanolysis method over a solid base catalyst at the bench scale, and the Wilson model was used to account for the nonideality of the liquid phase. The superiority of the catalytic distillation on the removal of the products to restrain the reverse reaction was illustrated in the present work. Furthermore, the influence of total pressure and the reaction temperature on DMC yield and the sensitivity analysis to the reaction kinetics were discussed in detail. The results revealed that the catalytic distillation was appropriate for the process of DMC synthesis.



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Synthesis of dimethyl carbonate from urea and methanol using polyphosphoric acid as catalyst
Jianjun Suna, Bolun Yang, Xiaoping Wanga, Dongpeng Wanga and Hongye Lin
Journal of Molecular Catalysis A: Chemical Volume 239, Issues 1-2, 14 September 2005, Pages 82-86



Abstract
A new process was proposed for the synthesis of dimethyl carbonate (DMC) from urea and methanol in a batch operation. Polyphosphoric acid (PPA) was used as the catalyst and the absorbent for the ammonia, which was produced during the reaction. The effects of various operation conditions, such as reaction temperature, pressure, reaction time and the molar ratio of the reactants were investigated in the terms of DMC yield. The experimental results indicated that the optimal reaction conditions were the molar ratio of methanol/urea of 14, reaction time of 4 h, reaction temperature of 413 K, PPA/urea mass ratio of 1 and initial pressure of CO2 of 0.8 MPa, respectively. The DMC yield of 67.4% was obtained in the optimal reaction conditions. The by-product, ammonia was also used as a starting material of a useful fertilizer in the proposed process.



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Reactive rectifying for producing dimethyl carbonate
Xiaoping Wanga, Bolun Yang, Dongpeng Wanga and Xiaowei Zhai
Chemical Engineering JournalVolume 122, Issues 1-2, 1 September 2006, Pages 15-20[/i]




Abstract
A process for producing dimethyl carbonate (DMC) from methanol and urea, using polyphosphoric acid (PPA) as the catalyst, has been carried out by conducting the reaction continuously under reactive rectifying conditions on a laboratory scale. Several operational variables which have an influence on the yield of DMC, such as the total feed flow rate, bottom temperature, pressure, reflux ratio, mass ratio of the reactants, the concentration of the catalyst and the stirring speed, were investigated to achieve an optimum operation. Under these optimized settings, the highest yield of DMC obtained was 92.2%. A high concentration and purity of DMC in the overhead products, more than 17%, was gained in the reactive rectifying conditions



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Synthesis of dimethyl carbonate from urea and methanol catalyzed by the metallic compounds at atmospheric pressure
Bolun Yang, Dongpeng Wang, Hongye Lin, Jianjun Sun and Xiaoping Wang
Catalysis Communications Volume 7, Issue 7, July 2006, Pages 472-477 [/i]



Abstract
A novel route was proposed for producing dimethyl carbonate (DMC) at atmospheric pressure from urea and methanol catalyzed by the metallic compounds with a high boiling point electron donor compounds (polyethylene glycol dimethyl ether) (PGDE) as solvent. The effects of various operation conditions, such as methanol/urea initial molar ratio, catalyst concentration, urea/PGDE initial mass ratio, flow rate of circulating, reaction temperature, stirring speed and reaction time on DMC yield were investigated, respectively. Experimental results indicate that the using of PGDE as solvent enable this synthesis reaction to reach the requisite temperature and restrain the decomposition of urea and MC; removing the products, DMC and ammonia effectively from the reaction system in time is important to improve the yield of DMC. The DMC yield of 28.8% can be obtained in the optimal reaction conditions. This new process shows some advantages such as easily operating, effectively removing NH3 from the reaction system and lower cost.   




¡Prefiero morir de pie que vivir siempre arrodillado!.Emiliano ZapataIt is better to die on your feet than to live on your knees!.......

POSEIDON

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Re: Wanted References and Translations
« Reply #182 on: December 30, 2009, 02:28:11 AM »
THE LABORATORY PREPARATION OF DIETHYL SULFATE
E. V. Lynn, H. A. Shoemaker
J. Am. Chem. Soc., 1924, 46 (4), pp 999–1001
DOI: 10.1021/ja01669a023
« Last Edit: June 20, 2011, 08:33:51 AM by Enkidu »
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Quantum Dude

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Re: Wanted References and Translations
« Reply #183 on: December 30, 2009, 06:09:45 AM »
Nature of N-Bromosuccinimide in Basic Media: The True Oxidizing Species in the Hofmann Rearrangement

Chris H. Senanayake, Laura E. Fredenburgh, Robert A. Reamer, Robert D. Larsen, Thomas R. Verhoeven, Paul J. Reider
J. Am. Chem. Soc., 1994, 116 (17), pp 7947–7948
DOI: 10.1021/ja00096a082
Publication Date: August 1994

http://pubs.acs.org/doi/pdf/10.1021/ja00096a082
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Development of a Scalable Synthesis of Dipeptidyl Peptidase-4 Inhibitor ABT-279

Todd S. McDermott*†, Lakshmi Bhagavatula‡, Thomas B. Borchardt§, Kenneth M. Engstrom‡, Jorge Gandarilla‡, Brian J. Kotecki‡, Albert W. Kruger‡, Michael J. Rozema‡, Ahmad Y. Sheikh§, Seble H. Wagaw‡ and Steven J. Wittenberger‡
Org. Process Res. Dev., 2009, 13 (6), pp 1145–1155
DOI: 10.1021/op900197r
Publication Date (Web): October 15, 2009
Copyright © 2009 American Chemical Society

A convergent, scalable synthesis of dipeptidyl peptidase-4 inhibitor, ABT-279, has been developed and demonstrated on multikilogram scale. The cis-2,5-disubstituted pyrrolidine is generated by cyclization of a Boc-amine onto an alkynyl ketone followed by stereospecific reduction of the resulting acyliminium intermediate. The amine coupling partner was prepared by a novel Hofmann rearrangement promoted by 1,3-dibromo-5,5-dimethylhydantoin. The final product was isolated as the l-malic acid salt. The scale-up campaign consisted of 15 steps and delivered 42 kg of ABT-279 in 14% overall yield. A second-generation synthesis that addresses some of the issues encountered during scale-up was developed and demonstrated on kilogram scale.

http://pubs.acs.org/doi/abs/10.1021/op900197r

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Hofmann rearrangement by using n-bromophthalimide-silveracetate in DMF
Min-Soo Park and Chang-Uk Choi
College of Pharmacy, I(yungsun# University, Pusan 608-736, Korea)

By using N-bromophthalimide (NBP) as halonium ion source for the Hofmann rearrangement,
a series of primary amide could be converted to the corresponding carbamate in excellent
yields. So NBP was thought to be very effective and practical halonium ion source for the
Hofmann rearrangement.

http://www.springerlink.com/content/c14023t87v379g85/

8)
Gracias java !
« Last Edit: June 20, 2011, 08:33:10 AM by Enkidu »

no1uno

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Re: Wanted References and Translations
« Reply #184 on: December 30, 2009, 09:21:00 AM »


Simultaneous Synthesis of Dimethyl Carbonate and Poly(ethylene terephthalate) Using Alkali Metals as Catalysts
Dan ZHANGa, b, Qingyin WANGa, Jie YAOa, Yue WANGa, Yi ZENGa and Gongying WANG
Chinese Journal of Chemical Engineering
2007,Volume 15, Issue 5, Pages 772-774
DOI: 10.1016/S1004-9541(07)60161-X



Abstract  
Dimethyl carbonate (DMC) and poly(ethylene terephthalate) was simultaneously synthesized by the transesterification of ethylene carbonate (EC) with dimethyl terephthalate (DMT) in this paper. This reaction is an excellent green chemical process without poisonous substance. Various alkali metals were used as the catalysts. The results showed alkali metals had catalytic activity in a certain extent. The effect of reaction condition was also studied. When the reaction was carried out under the following conditions: the reaction temperature 250°C, molar ratio of EC to DMT 3:1, reaction time 3h, and catalyst amount 0.004 (molar ratio to DMT), the yield of DMC was 68.9%.  
« Last Edit: January 04, 2010, 02:41:56 AM by java »
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java

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Re: Wanted References and Translations
« Reply #185 on: December 31, 2009, 03:34:22 PM »


Chemical Recycling of Poly(ethylene terephthalate)
Daniel Paszun and Tadeusz Spychaj
Ind. Eng. Chem. Res. 1997, 36 (4), pp 1373–1383
DOI: 10.1021/ie960563c



Abstract
This paper reviews the state of the art in the field of chemical recycling of poly(ethylene terephthalate) (PET). Advantages of the chemical recycling of PET, the theoretical basis of the ester bond cleavage, and a wide spectrum of degrading agents and final products are presented. Chemical processes applied in polymer recycling are divided into six groups:  methanolysis, glycolysis, hydrolysis, ammonolysis, aminolysis, and other methods. Numerous possibilities for the utilization of waste PET as a very useful raw chemical material are described on the basis of literature. A comparison of chemical recycling methods is carried out. The following aspects were taken into consideration:  (i) flexibility in utilizing a variety of waste types, (ii) conditions necessary for degradation including safety requirements, (iii) economic aspects, and (iv) product versatility. A total of 108 references including 46 patents are cited in this paper.


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Theoretical study of the transesterification reaction of polyethylene terephthalate under basic conditions
Yusuke Asakuma, Kyuya Nakagawaa, Kouji Maedaa and Keisuke Fukuia
Polymer Degradation and StabilityVolume 94, Issue 2, February 2009, Pages 240-245
DOI: 10.1016/j.polymdegradstab.2008.10.029



Abstract
The depolymerization reaction of polyethylene terephthalate (PET) was analyzed using a computational chemistry approach. The reaction is a type of transesterification reaction using alkoxide. In this study we employed the calculated optimum structure, electrostatic potential distribution, activation energy, electric charges and pathway to investigate the mechanism. We found that the tetrahedral intermediate produced by ring formation with alkoxide is an essential feature of the depolymerization process. Moreover, there is a possibility that a PET molecule is depolymerized by multiple alkoxides at the same time. However, the effects of degree of polymerization and the position of attack by the alkoxides do not strongly influence the reactivity.




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Transesterification of urea and ethylene glycol to ethylene carbonate as an important step for urea based dimethyl carbonate synthesis
Bhalchandra M. Bhanage, Shin-ichiro Fujita, Yutaka Ikushima and Masahiko Arai
Green Chem. 2003, 5, pp.429-432
DOI: 10.1039/b304182d



Abstract
Two-step synthesis of dimethyl carbonate (DMC) from urea has been investigated with various solid catalysts. The first step involves reaction of urea with ethylene glycol (EG) to form ethylene carbonate (EC) and the second step transesterification of EC formed with methanol to give DMC and EG. It has been found that ZnO is highly active and selective for the two steps, of which the former should be conducted under reduced pressure. At around ambient pressure, 2-oxazolidone and ethyleneurea are formed in the first step. Similar to EG, other glycols such as 1,2- and 1,3-propanediols can also be transformed to corresponding cyclic carbonates.




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Synthesis of ethylene carbonate from urea and ethylene glycol over zinc/iron oxide catalyst
Zhao, Xinqiang; An, Hualiang; Wang, Shufang; Li, Fang; Wang, Yanji
Journal of Chemical Technology & BiotechnologyVolume 83(5) May 2008 , pp.750-755(6)
DOI: 10.1002/jctb.1872



Abstract
BACKGROUND: Ethylene carbonate (EC) was synthesised via urea and ethylene glycol (EG) over zinc/iron oxide catalyst. By so doing, the by-product, EG, generated in the process of producing dimethyl carbonate by the transesterification route was converted back to the raw material, EC. The reaction mechanism of EC synthesis was also investigated by means of gas chromatography/mass spectrometry and in situ Fourier transform infrared/attenuated total reflection spectroscopy.

RESULTS: Suitable conditions for the preparation of zinc/iron oxide catalyst were as follows: zinc acetate and iron nitrate as precursors, Zn/Fe molar ratio 8:1, calcination temperature 350 °C and calcination time 4 h. Characterisation by X-ray diffraction revealed two different crystal phases: ZnO and ZnFe2O4. The highest yield of EC (66.1%) was obtained under the following conditions: reaction temperature 150 °C, reaction time 2.5 h, catalyst weight percentage 1.5% and urea/EG molar ratio 1:8. The study of the reaction mechanism revealed that the reaction for the synthesis of EC proceeded in two steps.



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High performance method for O-methylation of phenol with dimethyl carbonate
Samedy Ouka, Sophie Thiébaud, Elisabeth Borredona and Pierre Le Gars
Applied Catalysis A: GeneralVolume 241, Issues 1-2, 20 February 2003, Pages 227-233
DOI: 10.1016/S0926-860X(02)00467-2 



Abstract
The O-methylation of phenols, including the sterically hindered phenols, with dimethyl carbonate (DMC) under mild conditions of temperature and pressure was described. The reaction was carried out in the presence of tetrabutylammonium bromide (TBAB), in a semi-continuous process. Aryl methyl ethers were rapidly and selectively obtained in good yields.



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O-Methylation of phenolic compounds with dimethyl carbonate under solid/liquid phase transfer system
Samedy Ouka, Sophie Thiebauda, Elisabeth Borredona, Pierre Legarsb and Loic Lecomteb
Tetrahedron LettersVolume 43, Issue 14, 1 April 2002, Pages 2661-2663
DOI: 10.1016/S0040-4039(02)00201-0



Abstract
The industrially important alkyl aryl ethers, of which anisole is the simplest form, can be synthesized by reacting the corresponding phenols with the environmentally benign dimethyl carbonate (DMC). The reaction is carried out under mild conditions of temperature and pressure. Excellent yields and selectivity of product were obtained after a few hours of reaction.

¡Prefiero morir de pie que vivir siempre arrodillado!.Emiliano ZapataIt is better to die on your feet than to live on your knees!.......

java

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Re: Wanted References and Translations
« Reply #186 on: December 31, 2009, 03:41:17 PM »

Oxidative coupling of cis-3,N-bis(methoxycarbonyl)-N-norreticuline. An approach to the asymmetric synthesis of morphine alkaloids
Martin A. Schwartz, Pham Phuong Thi Kim
J. Org. Chem.1988, 53 (10), pp 2318–2322
DOI: 10.1021/jo00245a035



Abstract
Racemic 3,N-bis(methoxycarbonyl)-N-Norreticuline (1) synthesized from (+,-)-3-methoxytyrosine by the Bischler-Napieralski route, was shown to have cis stereochemistry by X-ray crystallography. Oxidative coupling of the title compound with iodosobenzene in the presence of trifluoroacetic acid gave results virtually identical with those obtained from the corresponding norreticuline derivative lacking the C-3 methoxycarbonyl substituent; the substituted norsalutaridine and norisoboldine derivatives 2 and 3 were isolated in yields of 25% and 21%, respectively, along with 9% of uncoupled quinone 10 and 36% recovered starting material. Similar comparative oxidative coupling studies were carried out with C-3 substituted and unsubstituted norreticulines using vanadium oxytrichloride and thallium (III) trifluoroacetate as oxidizing agents. Racemic 16,N-bis(methoxycarbonyl)-norsalutaridine (2) was converted to the corresponding 16-(methoxycarbonyl)-northebaine derivative 12 by standard methods (76% yield). The latter was decarboxylated, hydrolyzed, and reduced to afford (+,-)-codeine (14) (34% overall yield). Application of the Bishcler-Napieralski synthetic approach to (R)-(+)-3-methoxytyrosine afforded (1R,3R)-(-)3,N-bis(methoxycarbonyl)-N-norreticuline in 54% ee. Oxidative coupling of the latter with iodosobenzene diacetate and trifluoroacetic acid gave the (9R)-(+)-norsalutaridine derivative with no detectable loss in optical purity.




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Synthesis and oxidative coupling of (.+-.)-3-oxoreticuline
Douglas G. Vanderlaan, Martin A. Schwartz
J. Org. Chem. 1985, 50 (6), pp 743–747
DOI: 10.1021/jo00206a003



Abstract
The synthesis and oxidative coupling of 3-oxoreticuline (8) are described. Reaction of 8 with iodosobenzene diacetate in the presence of trifluoroacetic acid gave 16-oxosalutaridine (12), 16-oxopallidine (13), 5-oxoisoboldine (14), and 13-oxothalidine (15) in yields of 27%, 8%, 6% and 10% respectively. Oxidation of 8 with vanadium oxytrichloride gave 13, 14, and 15 in yields of 26%, 11% and 9% respectively.
¡Prefiero morir de pie que vivir siempre arrodillado!.Emiliano ZapataIt is better to die on your feet than to live on your knees!.......