Academic literature on the topic '1-Allyl-2'

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Journal articles on the topic "1-Allyl-2"

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Seethalakshmi, T., P. Venkatesan, M. Nallu, Daniel E. Lynch, and S. Thamotharan. "1-Allyl-2-aminopyridin-1-ium bromide." Acta Crystallographica Section E Structure Reports Online 69, no. 6 (May 15, 2013): o884. http://dx.doi.org/10.1107/s1600536813012452.

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Nirmala, S., E. Theboral Sugi Kamala, L. Sudha, A. R. Naresh Raj, and C. A. M. A. Huq. "1-Allyl-3,3-diphenylindolin-2-one." Acta Crystallographica Section E Structure Reports Online 64, no. 5 (April 16, 2008): o834. http://dx.doi.org/10.1107/s1600536808009446.

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Li, Dong-Ping, Min Li, Shuai Li, and Hang-Na Hu. "(±)-1-(1-Allyl-1H-benzimidazol-2-yl)ethanol." Acta Crystallographica Section E Structure Reports Online 68, no. 12 (November 3, 2012): o3254. http://dx.doi.org/10.1107/s1600536812044340.

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Benzeid, Hanane, Rachid Bouhfid, Stephane Massip, Jean Michel Leger, and El Mokhtar Essassi. "1-Allyl-3-phenylquinoxalin-2(1H)-one." Acta Crystallographica Section E Structure Reports Online 67, no. 11 (October 22, 2011): o2990. http://dx.doi.org/10.1107/s1600536811042474.

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Eltayeb, Naser Eltaher, Siang Guan Teoh, Suchada Chantrapromma, and Hoong-Kun Fun. "4-Allyl-2-[1-(5-allyl-2-hydroxy-3-methoxybenzyl)-1H-benzimidazol-2-yl]-6-methoxyphenol pyridine solvate." Acta Crystallographica Section E Structure Reports Online 63, no. 10 (September 26, 2007): o4141—o4142. http://dx.doi.org/10.1107/s1600536807046065.

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Xu, Xiong-Bin, and Qiong Ye. "3-Allyl-1-(2-cyanobenzyl)-2-methylbenzimidazol-3-ium bromide." Acta Crystallographica Section E Structure Reports Online 64, no. 1 (December 6, 2007): o23. http://dx.doi.org/10.1107/s1600536807060874.

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Nirmala, S., E. Theboral Sugi Kamala, L. Sudha, A. R. Naresh Raj, and C. A. M. A. Huq. "1-Allyl-3,3-di-p-tolylindolin-2-one." Acta Crystallographica Section E Structure Reports Online 64, no. 5 (April 23, 2008): o879. http://dx.doi.org/10.1107/s1600536808010088.

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Belaziz, Dounia, Youssef Kandri Rodi, Fouad Ouazzani Chahdi, El Mokhtar Essassi, Mohamed Saadi, and Lahcen El Ammari. "1-Allyl-1H-1,3-benzimidazol-2(3H)-one." Acta Crystallographica Section E Structure Reports Online 68, no. 11 (October 27, 2012): o3212. http://dx.doi.org/10.1107/s1600536812043620.

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Radi, Smaail, and Hassan Lazrek. "1-[(2-Acetoxyethoxy)methyl]-3-allyl-6-azauracil." Molecules 5, no. 12 (April 28, 2000): M151. http://dx.doi.org/10.3390/m151.

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Alsubari, Abdulsalam, Ahmed Moussaif, Hafid Zouihri, El Mokhtar Essassi, and Seik Weng Ng. "N′-(1-Allyl-2-oxoindolin-3-ylidene)benzohydrazide." Acta Crystallographica Section E Structure Reports Online 66, no. 8 (July 3, 2010): o1905. http://dx.doi.org/10.1107/s1600536810024918.

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Dissertations / Theses on the topic "1-Allyl-2"

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Uiterweerd, Patrick Gerard Herman. "2,6-bis(dimethylamino)phenyl and 1-aza-2-phospha(V)allyl main group metal chemistry." Thesis, University of Sussex, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.366076.

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Foucart, Quentin. "Etude de la débenzylation régiosélective en position 2 de 1-C-allyl iminosucres pour l'introduction de diversité moléculaire." Thesis, Poitiers, 2018. http://www.theses.fr/2018POIT2318.

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Parmi les analogues de sucres, les iminosucres constituent la classe la plus prometteuse au niveau biologique. En effet, leur structure, dans laquelle l'atome d'oxygène intracyclique est remplacé par un atome d'azote, leur confère des propriétés uniques d'inhibition de glycosidases et/ou glycosyltransférases, et en fait donc de très bons candidats thérapeutiques. L'introduction d'un substituant pseudo-anomérique carboné permet de mimer la partie aglycone du substrat de l'enzyme et d'accéder aux iminosucres C-glycosides, des composés chimiquement stables qui sont des inhibiteurs sélectifs et puissants des glycosidases.Afin d'accélérer la découverte de molécules d'intérêt thérapeutique, il est nécessaire de trouver des voies de synthèses conduisant à une plus grande diversité structurale. La méthodologie que nous avons mise au point est basée sur la débenzylation régiosélective de la position 2 de C-allyl glycosides exploitant une iodocyclisation. Cette dernière a été appliquée avec succès à la C-allyl-1-déoxynojirimycine puis étendue à plusieurs iminosucres de configurations variées en séries pipéridine et pyrrolidine.L'introduction de diversité moléculaire a été réalisée à partir de la C-allyl-1-déoxynojirimycine O-débenzylée régiosélectivement en position 2. Nous avons ainsi obtenu plusieurs iminosucres de configurations D-gluco- et D-manno- portant différentes fonctionnalités en position 2. La mise au point de cette synthèse a donc permis d'accéder à une grande variété de C-allyl iminosucres à partir d'un synthon unique. L'accès à des iminosucres bicycliques de structures inédites a également été possible en exploitant un C-allyl 2-céto iminosucre obtenu par notre méthodologie de débenzylation régiosélective
Iminosugars constitute undoubtedly the most promising class of sugar analogues, their unique glycosidase and/or glycosyltransferase inhibition profile making them promising therapeutics. To generate more potent and selective inhibitors called C-glycoside iminosugars, introduction of a stable pseudoanomeric substituent is usually performed, the improved efficacy being attributed in part to the information brought by the aglycon moiety.The main challenge associated with this class of iminosugars C-glycosides is currently the design of efficient and general routes enabling introduction of structural diversity at a late stage from advanced synthons to accelerate the discovery of biologically relevant molecules. In this context, we have explored a strategy based on a regioselective debenzylation at C-2 and a stereocontrolled nucleophilic substitution assisted by the N-benzyl group. We have successfully applied this methodology on the C-allyl-1-deoxynojirimycin and extended it to several iminosugars in the piperidine and pyrrolidine series.The introduction of molecular diversity was performed from the C-allyl-1-deoxynojirimycin selectively O-debenzylated at position 2. We obtained several iminosugars in the D-gluco- and D-manno- series bearing various functionalities at position 2. This strategy allowed us to access a wide range of C-allyl iminosugars from one single synthon. We have also described the access to unknown bicyclic iminosugars starting from a C-allyl 2-keto iminosugar obtained by our regioselective debenzylative methodology
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Swigelaar, Wendell Peter. "The synthesis of 3-allyl-4-ethyl-2- (1'-hydroxyethyl)-1-methoxynaphthalene and its behaviour towards base- and palladium-promoted cyclisation under aerobic and anaerobic conditions." Thesis, University of the Western Cape, 2005. http://etd.uwc.ac.za/index.php?module=etd&amp.

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Over the years, Giles and co-workers have established that, upon treatment with potassium tert-butoxide, tetra-substituted naphthalenes undergo cyclisations to afford naphthopyrans. It was suggested that these base-induced cyclisations was as a result of the reacting centers being forced into close proximity as a consequence of steric crowding.

This thesis describes the synthesis of 3-allyl-4-ethyl-2-(1&prime
-hydroxyethyl)-1-methoxy-naphthalene 177 and its behaviour towards Pd(0) and potassium tert-butoxide under aerobic and anaerobic conditions, to verify whether the base-promoted cyclisations are indeed caused by the steric influences of the substituents. Two synthetic routes were attempted in the synthesis of the target naphthalene 177. The first of these attempted routes involved the conversion of 2-acetyl-4-hydroxy-1-methoxynaphthalene 182 into 2-acetyl-1-methoxy-4-trifluoromethanesulphonyloxy-naphthalene 191 and subsequently into 2-acetyl-4-ethyl-1-methoxynaphthalene 192 via Stille coupling. However, the subsequent Snieckus ortho-directed metalation reactions on the reduced 4-ethyl-2-(1&prime
-hydroxyethyl)-1-methoxynaphthalene 193, and analogues of it, to afford naphthalene 177 were unsuccessful. The second route entailed a Claisen rearrangement of the tri-substituted 2-acetyl-4-allyloxy-1-methoxynaphthalene 209 to afford the unstable tetra-substituted 2-acetyl-3-allyl-4-hydroxy-1-methoxynaphthalene 210, which was immediately converted into the corresponding 2-acetyl-3-allyl-1-methoxy-4-trifluoromethanesulpholnyloxynaphthalene 211. Stille coupling of the triflate 211 gave the 2-acetyl-3-allyl-4-ethyl-1-methoxy-naphthalene 212, which was subsequently reduced to the target naphthalene alcohol 177.
The base-induced cyclisation studies performed on naphthalene 177, confirmed the hypothesis that these cyclisations of terta-substituted naphthalenes are indeed as a result of steric crowding.
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Lima, Luis Ferreira de. "Obten??o de ?lcool al?lico (PROP-2-EN-1-OL) a partir da glicerina derivada do biodiesel de ?leo de mamona." Universidade Federal do Rio Grande do Norte, 2012. http://repositorio.ufrn.br:8080/jspui/handle/123456789/13016.

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In this work, biodiesel was produced from castor oil that was a byproduct glycerin. The molar ratio between oil and alcohol, as well as the use of (KOH) catalyst to provide the chemical reaction is based on literature. The best results were obtained using 1 mol of castor oil (260g) to 3 moles of methyl alcohol (138g), using 1.0% KOH as catalyst at a temperature of 260 ? C and shaken at 120 rpm. The oil used was commercially available, the process involves the reaction of transesterification of a vegetable oil with methyl alcohol. The product of this reaction is an ester, biodiesel being the main product and the glycerin by-product which has undergone treatment for use as raw material for the production of allyl alcohol. The great advantage of the use of glycerin to obtain allyl alcohol is that its use eliminates the large amount of waste of the biodiesel and various forms of insult to the environment. The reactions for the formation of allyl alcohol was conducted from formic acid and glycerin in a ratio 1/1, at a temperature of 260oC in a heater blanket, being sprayed by a spiral condenser for a period of 2 hours and the product obtained contains mostly the allylic alcohol .. The monitoring of reactions was performed by UV-Visible Spectrophotometer: FTIR Fourier transform, the analysis showed that these changes occur spectrometer indicating the formation of the product allylic alcohol (prop-2-en-1-ol) in the presence of water, This alcohol was appointed Alcohol GL. The absorption bands confirms that the reaction was observed in (? C = C) 1470 -1600 cm -1 and (? CO), 3610-3670 attributed to C = C groups and OH respectively. The thermal analysis was carried out in a thermogravimetric analyzer SDT Q600, where the mass and temperature are displayed against time, that allows checking the approximate rate of heating. The innovative methodology developed in the laboratory (LABTAM, UFRN), was able to treat the glycerine produced by transesterification of castor oil and used as raw material for production of allyl alcohol, with a yield of 80%, of alcohol, the same is of great importance in the manufacture of polymers, pharmaceuticals, organic compounds, herbicides, pesticides and other chemicals
Neste trabalho o biodiesel foi produzido a partir de ?leo de mamona que teve como subproduto a glicerina. A raz?o molar entre ?leo e ?lcool, bem como o uso do (KOH) como catalisador qu?mico para proporcionar a rea??o, foi baseada em dados da literatura. Os melhores resultados foram obtidos, utilizando 1 mol de ?leo de mamona (260g) para 3 mols de ?lcool met?lico (138g). O ?leo utilizado foi adquirido comercialmente, o processo de transesterifica??o envolve a rea??o do ?leo vegetal com um ?lcool met?lico. O produto dessa rea??o ? um ?ster, sendo o biodiesel o seu principal produto e a glicerina o sub-produto a qual foi submetida a tratamento para uso como mat?ria-prima para a obten??o do ?lcool al?lico. A grande vantagem do uso da glicerina para obten??o de ?lcool al?lico ? que sua utiliza??o elimina a grande quantidade de res?duos do biodiesel e v?rias formas de agress?o ao meio ambiente. As rea??es para forma??o do ?lcool alilico foram conduzidas a partir de ?cido f?rmico e glicerina, em uma raz?o 1/1, sob temperatura de 260oC, em uma manta aquecedora, sendo vaporizado por um condensador em espiral por um per?odo de 2 horas, e o produto obtido contem em sua grande maioria o ?lcool al?lico. O acompanhamento das rea??es foi realizado por Espectrofot?metro UV-Vis?vel: FTIR com transformada de Fourier, a an?lise revelou que estas altera??es espectrom?tricas ocorrem indicando a forma??o do produto ?lcool al?lico (prop-2-en-1-ol), em presen?a de ?gua, este ?lcool foi nomeado de ?lcool GL. As bandas de absor??o que confirmam a rea??o foram observadas em (? C=C) em 1470 -1600 cm-1 e em (? C-O), 3610 3670 atribu?das aos grupos C=C e O-H respectivamente. A analise t?rmica foi realizada em um analisador Termogravim?trico SDT Q600, onde a massa e a temperatura ser?o exibidos em fun??o do tempo, isto permite a verifica??o aproximada da taxa de aquecimento. A metodologia inovadora desenvolvida no laborat?rio (LABTAM, UFRN), foi capaz de tratar a glicerina produzida, atrav?s da transesterifica??o de ?leo de mamona e utilizar como mat?ria prima para produ??o do ?lcool al?lico, apresentando um rendimento de 80%, deste ?lcool, o mesmo ? de grande import?ncia na fabrica??o de pol?meros, medicamentos, compostos org?nicos, herbicidas, pesticidas e outros produtos qu?micos
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Huang, Yeun-Chih, and 黃允志. "Effects of GPEUC ( 1-[(4-allyl-2-methoxy-) phenoxy]-3-[(2- methoxy phenoxyethyl)-amino]-propanol ) on cardiovascular system." Thesis, 1995. http://ndltd.ncl.edu.tw/handle/90560911198536886108.

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Book chapters on the topic "1-Allyl-2"

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Winkelmann, J. "Diffusion of carbon dioxide (1); 4-allyl-2-methoxy-phenol (2)." In Gases in Gases, Liquids and their Mixtures, 1918. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1465.

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Wohlfarth, Ch. "Refractive index of the mixture (1) methanol; (2) allyl acetate." In Refractive Indices of Pure Liquids and Binary Liquid Mixtures (Supplement to III/38), 744. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75291-2_475.

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Wohlfarth, Ch. "Refractive index of the mixture (1) vinyl acetate; (2) allyl acetate." In Refractive Indices of Pure Liquids and Binary Liquid Mixtures (Supplement to III/38), 1330. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75291-2_842.

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Holze, Rudolf. "Ionic conductivities of 1-ally-2-methyl-3-allyl-imidazolium bis(trifluoromethylsulfonyl)imide." In Electrochemistry, 120. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-02723-9_94.

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Trattnig, N., P. Kosma, and A. Ni Cheallaigh. "Synthesis of Allyl α-(1→2)-Linked α-Mannobioside from a Common 1,2-Orthoacetate Precursor." In Carbohydrate Chemistry, 99–108. Boca Raton : CRC Press, 2020. | Series: Proven synthetic methods ; volume 5: CRC Press, 2021. http://dx.doi.org/10.1201/9781351256087-13.

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Larsen, R. D., and D. Cai. "From 1-(2-Haloaryl)allyl Acetates." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-00705.

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lvarez, M., and J. A. Joule. "Synthesis of Phenyl 1-Allyl-1,2-dihydroisoquinoline-2-carboxylates." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01309.

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Nelson, A. "Synthesis of 2-1-Benzothiopyran-2-thiones by Rearrangement of Allyl Phenyl Sulfides and Oxidation." In Six-Membered Hetarenes with One Chalcogen, 1. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-014-00972.

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Taber, Douglass. "The Keck Synthesis of Epothilone B." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0101.

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The total synthesis of Epothilone B 4, the first natural product (with Epothilone A) to show the same microtubule-stabilizing activity as paclitaxel (Taxol®), has attracted a great deal of attention since that activity was first reported in 1995. The total synthesis of 4 devised (J. Org. Chem. 2008, 73, 9675) by Gary E. Keck of the University of Utah was based in large part on the stereoselective allyl stannane additions (e.g. 1 + 2 → 3 ) that his group originated. The allyl stannane 2 was prepared from the acid chloride 5. Exposure of 5 to Et3N generated the ketene, that was homologated with the phosphorane 6 to give the allene ester 7. Cu-mediated conjugate addition of the stannylmethyl anion 8 then delivered 2. The silyloxy aldehyde 1 was prepared from the ester 9 by reduction with Dibal. Felkincontrolled 1,2-addition of the allyl stannane 2 established the relative configuration of the secondary alcohol of 3, that was then used to control the relative configuration of the new alcohol in 10. Addition of the crotyl borane 12 to the derived aldehyde 11 also proceeded with high diastereocontrol. The other component of 4 was prepared from the aldehyde 14. Enantioselective allylation, by the method the authors developed, delivered the alcohol 16. The Z trisubstituted alkene was then assembled by condensing the aldehyde 17 with the phosphorane 18. Dibal reduction of the product lactone 19 gave a diol, the allylic alcohol of which was selectively converted to the chloride with the Corey-Kim reagent. Hydride reduction then delivered the desired homoallylic alcohol, that was converted to the phosphonium salt 21. Condensation of 21 with 13 gave the diene, that was carried on to Epothilone B 4. The synthesis of Epothilone B 4 as originally conceived by the authors depended on ring-closing metathesis of the triene 22. They prepared 22, but on exposure to the second-generation Grubbs catalyst it was converted only to 23. The authors concluded that the trans acetonide kept 22 in a conformation that did not allow the desired macrocyclization.
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Mikami, K., Y. Matsumoto, and T. Shiono. "(η-Allyl)bis(η-cyclopentadienyl)halotitanium(IV) Complexes by Reaction of (η-Allyl)bis(η-cyclopentadienyl)titanium(III) Complexes with 1-Halobut-2-enes." In Compounds of Groups 7-3 (Mn..., Cr..., V..., Ti..., Sc..., La..., Ac...), 1. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-002-00654.

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Conference papers on the topic "1-Allyl-2"

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Reza, Md, Jinjun Liu, Jahangir Alam, Anam Paul, and Hamzeh Telfah. "CAVITY RING-DOWN SPECTROSCOPY OF 1-, 2- AND 3-METHYL ALLYL PEROXY RADICALS." In 73rd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2018. http://dx.doi.org/10.15278/isms.2018.mj11.

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Mirghani, Mohamed, Adeeb Hayyan, Hanee Hizaddin, Mahar Diana Hamid, Jehad Saleh, M. Y. Zulkifli, Waleed Al Abdulmonem, Fahad Alhumaydhi, and Abdullah Aljohani. "Novel Encapsulated Ionic Liquid Analogous for Free Fatty Acid Conversion to Fatty Acid Methyl Ester." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/vapq5899.

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The development of an efficient and green catalyst can be considered as a major contribution for the esterification of free fatty acid (FFA) in non-edible oil feedstocks. The DES was encapsulated in medical capsules for esterification of free fatty acid. The DES was synthesized from allyltriphenylphosphonium bromide (Allyl) and p-toluenesulfonic acid (PTSA). The FFA content was reduced to < 2 % under optimum conditions (catalyst dosage 2% (wt/wt) catalyst to oil, 10:1 molar ratio of oil to methanol at 60 °C for 60 min reaction time). The formation of a eutectic mixture endows the catalyst with advantages for esterification reaction such as improvements in recyclability and hygroscopicity of PTSA.
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