Log in

Relevant bibliographies by topics / Furans Conversion / Journal articles

To see the other types of publications on this topic, follow the link: Furans Conversion.

Journal articles on the topic 'Furans Conversion'

Author: Grafiati

Published: 6 September 2023

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Furans Conversion.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Rivas, Sandra, María Jesús González-Muñoz, Valentín Santos, and Juan Carlos Parajó. "Production of furans from hemicellulosic saccharides in biphasic reaction systems." Holzforschung 67, no. 8 (2013): 923–29. http://dx.doi.org/10.1515/hf-2013-0017.

Full text

Abstract:

Abstract Furans (furfural and hydroxymethylfurfural) are the results of dehydration of monosaccharides, which can be obtained by acid hydrolysis of wood or other lignocellulosic materials. In this work, Pinus pinaster wood was subjected to aqueous autohydrolysis processing to obtain dissolved hemicellulose-derived polymeric or oligomeric saccharides made up of mannosyl, glucosyl, galactosyl, xylosyl, and arabinosyl structural units. The aqueous liquors were then heated in the presence of sulfuric acid and methyl isobutyl ketone to obtain furans. The effects of selected operational variables, s

APA, Harvard, Vancouver, ISO, and other styles

2

Yuliati, Frita, Peter J. Deuss, Hero J. Heeres, and Francesco Picchioni. "Towards Thermally Reversible Networks Based on Furan-Functionalization of Jatropha Oil." Molecules 25, no. 16 (2020): 3641. http://dx.doi.org/10.3390/molecules25163641.

Full text

Abstract:

A novel biobased monomer for the preparation of thermally reversible networks based on the Diels-Alder reaction was synthesized from jatropha oil. The oil was epoxidized and subsequently reacted with furfurylamine to attach furan groups via an epoxide ring opening reaction. However, furfurylamine also reacted with the ester groups of the triglycerides via aminolysis, thus resulting in short-chain molecules that ultimately yielded brittle thermally reversible polymers upon cross-linking via a Diels-Alder reaction. A full-factorial experimental design was used in finding the optimum conditions t

APA, Harvard, Vancouver, ISO, and other styles

3

Yang, Yanliang, Dongsheng Deng, Dong Sui, Yanfu Xie, Dongmi Li, and Ying Duan. "Facile Preparation of Pd/UiO-66-v for the Conversion of Furfuryl Alcohol to Tetrahydrofurfuryl Alcohol under Mild Conditions in Water." Nanomaterials 9, no. 12 (2019): 1698. http://dx.doi.org/10.3390/nano9121698.

Full text

Abstract:

The hydrogenation of furan ring in the biomass-derived furans is of great importance for the conversion of biomass to valuable chemicals. Fabrication of high activity and selectivity catalyst for this hydrogenation under mild conditions was one of the focuses of this research. In this manuscript, UiO-66-v, in which vinyl bonded to the benzene ring, was first prepared. Then, the uniformly distributed vinyl was used as the reductant for the preparation of Pd/UiO-66-v. The catalyst was characterized by X-ray diffraction, thermogravimetric, N2 physical adsorption/desorption, X-ray photoelectron sp

APA, Harvard, Vancouver, ISO, and other styles

4

Mao, Yanli, and François Mathey. "The Conversion of Furans into Phosphinines." Chemistry – A European Journal 17, no. 38 (2011): 10745–51. http://dx.doi.org/10.1002/chem.201100834.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Kumar, Hemant, and Marco Fraaije. "Conversion of Furans by Baeyer-Villiger Monooxygenases." Catalysts 7, no. 6 (2017): 179. http://dx.doi.org/10.3390/catal7060179.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Hu, Xun, Roel J. M. Westerhof, Liping Wu, Dehua Dong, and Chun-Zhu Li. "Upgrading biomass-derived furans via acid-catalysis/hydrogenation: the remarkable difference between water and methanol as the solvent." Green Chemistry 17, no. 1 (2015): 219–24. http://dx.doi.org/10.1039/c4gc01826e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Wang, Ting, Xianming Guo, Tao Chen, and Juan Li. "The Pd(0) and Pd(ii) cocatalyzed isomerization of alkynyl epoxides to furans: a mechanistic investigation using DFT calculations." Dalton Transactions 49, no. 27 (2020): 9223–30. http://dx.doi.org/10.1039/d0dt00965b.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Guillard, Jér̂ome, Otto Meth-Cohn, Charles W. Rees, Andrew J. P. White, and David J. Williams. "Direct conversion of macrocyclic furans into macrocyclic isothiazoles." Chemical Communications, no. 3 (January 17, 2002): 232–33. http://dx.doi.org/10.1039/b110287g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Pelter, Andrew, and Martin Rowlands. "The conversion of furans to 2(3H)-butenolides." Tetrahedron Letters 28, no. 11 (1987): 1203–6. http://dx.doi.org/10.1016/s0040-4039(00)95326-7.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Xu, Lujiang, Yuanye Jiang, Qian Yao, et al. "Direct production of indoles via thermo-catalytic conversion of bio-derived furans with ammonia over zeolites." Green Chemistry 17, no. 2 (2015): 1281–90. http://dx.doi.org/10.1039/c4gc02250e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

Laaman, Sean M., Otto Meth-Cohn, and Charles W. Rees. "The Ready Conversion of 2,5-Disubstituted Furans into Isothiazoles." Synthesis 1999, no. 05 (1999): 757–59. http://dx.doi.org/10.1055/s-1999-3480.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Parr, Brendan T., Samantha A. Green, and Huw M. L. Davies. "Rhodium-Catalyzed Conversion of Furans to Highly Functionalized Pyrroles." Journal of the American Chemical Society 135, no. 12 (2013): 4716–18. http://dx.doi.org/10.1021/ja401386z.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Matsagar, B. M., M. K. Munshi, A. A. Kelkar, and P. L. Dhepe. "Conversion of concentrated sugar solutions into 5-hydroxymethyl furfural and furfural using Brönsted acidic ionic liquids." Catalysis Science & Technology 5, no. 12 (2015): 5086–90. http://dx.doi.org/10.1039/c5cy00858a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Jaeger, M., and M. Mayer. "The Noell Conversion Process – a gasification process for the pollutant-free disposal of sewage sludge and the recovery of energy and materials." Water Science and Technology 41, no. 8 (2000): 37–44. http://dx.doi.org/10.2166/wst.2000.0140.

Full text

Abstract:

The Noell Conversion Process was developed to guarantee the safe disposal of sewage sludge and other waste materials by means of thermal treatment, evenwith very strict emission standards. The center piece of this process is a pressurized entrained flow gasifier. The reactin conditions in this gasifier does not only suppresses the formation of dioxins and furans, but also completely destroys any dioxins and furans contained in the waste materials. Another advantage of the Noell Conversion Process referring the thermal treatment of sewage sludge is the recovery of marketable substances such as

APA, Harvard, Vancouver, ISO, and other styles

15

Lang, Man, and Hao Li. "Value-added hydrodeoxygenation conversion of biomass." Biomass Science & Technology 1, no. 1 (2023): 1–8. http://dx.doi.org/10.61187/bst.v1i1.10.

Full text

Abstract:

Biomass hydrodeoxygenation conversion is an important technology for converting biomass waste into high-value-added chemicals and fuels. In this paper, the research progress of biomass hydrodeoxygenation conversion is reviewed, and the related catalysts and reactions are discussed. First, the background and significance of biomass hydrodeoxygenation conversion are introduced. Subsequently, the application of different catalysts in biomass hydrodeoxygenation conversion was discussed for different biomass feedstocks, such as phenols, ethers, acids, and furans. Finally, the challenges and future

APA, Harvard, Vancouver, ISO, and other styles

16

Hu, Xun, Sri Kadarwati, Yao Song, and Chun-Zhu Li. "Simultaneous hydrogenation and acid-catalyzed conversion of the biomass-derived furans in solvents with distinct polarities." RSC Advances 6, no. 6 (2016): 4647–56. http://dx.doi.org/10.1039/c5ra22414d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Briel, Detlef. "Synthesis and Conversion of 3-(2-Hydroxythiobenzamido)benzo[b]furans." HETEROCYCLES 65, no. 6 (2005): 1295. http://dx.doi.org/10.3987/com-04-10238.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Clive, Derrick L. J., Minaruzzaman та Ligong Ou. "Conversion of Furans into γ-Hydroxybutenolides: Use of Sodium Chlorite". Journal of Organic Chemistry 70, № 8 (2005): 3318–20. http://dx.doi.org/10.1021/jo0402935.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Zhou, Xuanmu, Zehui Zhang, Bing Liu, Quan Zhou, Shuguo Wang, and Kejian Deng. "Catalytic conversion of fructose into furans using FeCl3 as catalyst." Journal of Industrial and Engineering Chemistry 20, no. 2 (2014): 644–49. http://dx.doi.org/10.1016/j.jiec.2013.05.028.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Guillard, Jerome, Otto Meth-Cohn, Charles W. Rees, Andrew J. P. White, and David J. Williams. "ChemInform Abstract: Direct Conversion of Macrocyclic Furans into Macrocyclic Isothiazoles." ChemInform 33, no. 20 (2010): no. http://dx.doi.org/10.1002/chin.200220096.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Xia, Shengpeng, Chenyang Wang, Yu Chen, et al. "Sustainable Aromatic Production from Catalytic Fast Pyrolysis of 2-Methylfuran over Metal-Modified ZSM-5." Catalysts 12, no. 11 (2022): 1483. http://dx.doi.org/10.3390/catal12111483.

Full text

Abstract:

The catalytic fast pyrolysis (CFP) of bio-derived furans offers a promising approach for sustainable aromatic production. ZSM-5 modified by different metal species (Zn, Mo, Fe, and Ga) was employed in the CFP of bio-derived furans for enhancing aromatic production. The effects of metal species, metal loadings, and the weight hourly space velocity (WHSV) on the product distributions from the CFP of 2-methylfuran (MF) were systemically investigated. It is found that the introduction of Zn, Mo, Fe, and Ga on ZSM-5 significantly increases the MF conversion and aromatic yields. The maximum MF conve

APA, Harvard, Vancouver, ISO, and other styles

22

López, Mar, Carlos Vila, Valentín Santos, and Juan Carlos Parajó. "Manufacture of Platform Chemicals from Pine Wood Polysaccharides in Media Containing Acidic Ionic Liquids." Polymers 12, no. 6 (2020): 1215. http://dx.doi.org/10.3390/polym12061215.

Full text

Abstract:

Pinus pinaster wood samples were subjected to chemical processing for manufacturing furans and organic acids from the polysaccharide fractions (cellulose and hemicellulose). The operation was performed in a single reaction stage at 180 or 190 °C, using a microwave reactor. The reaction media contained wood, water, methyl isobutyl ketone, and an acidic ionic liquid, which acted as a catalyst. In media catalyzed with 1-butyl-3-methylimidazolium hydrogen sulfate, up to 60.5% pentosan conversion into furfural was achieved, but the conversions of cellulose and (galacto) glucomannan in levulinic aci

APA, Harvard, Vancouver, ISO, and other styles

23

Marshall, James A., and Gary S. Bartley. "Observations Regarding the Ag(I)-Catalyzed Conversion of Allenones to Furans." Journal of Organic Chemistry 59, no. 23 (1994): 7169–71. http://dx.doi.org/10.1021/jo00102a056.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Parr, Brendan T., Samantha A. Green, and Huw M. L. Davies. "ChemInform Abstract: Rhodium-Catalyzed Conversion of Furans to Highly Functionalized Pyrroles." ChemInform 44, no. 37 (2013): no. http://dx.doi.org/10.1002/chin.201337095.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Laaman, Sean M., Otto Meth-Cohn, and Charles W. Rees. "ChemInform Abstract: The Ready Conversion of 2,5-Disubstituted Furans into Isothiazoles." ChemInform 30, no. 35 (2010): no. http://dx.doi.org/10.1002/chin.199935147.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Zhu, Lijuan, Minghui Fan, Yulan Wang, Shengfei Wang, Yuting He, and Quanxin Li. "Selective conversion of furans to p ‐xylene with surface‐modified zeolites." Journal of Chemical Technology & Biotechnology 94, no. 9 (2019): 2876–87. http://dx.doi.org/10.1002/jctb.6090.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Zhang, Zehui, and Zongbao K. Zhao. "Microwave-assisted conversion of lignocellulosic biomass into furans in ionic liquid." Bioresource Technology 101, no. 3 (2010): 1111–14. http://dx.doi.org/10.1016/j.biortech.2009.09.010.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Barešić, Luka, Davor Margetić, and Zoran Glasovac. "Cycloaddition of Thiourea- and Guanidine-Substituted Furans to Dienophiles: A Comparison of the Environmentally-Friendly Methods." Chemistry Proceedings 3, no. 1 (2020): 57. http://dx.doi.org/10.3390/ecsoc-24-08380.

Full text

Abstract:

The cycloaddition strategy was employed in order to obtain a 7-oxanorbornene framework substituted with a guanidine moiety or its precursor functional groups: protected amine or thiourea. In order to optimize the conditions for the cycloaddition, several environmentally-friendly methods—microwave assisted organic synthesis, high pressure synthesis, high speed vibrational milling, and ultrasound assisted synthesis—were employed. The outcomes of the cycloaddition reactions were interpreted in terms of endo/exo selectivity, the conversion of the reactants to the product, and the isolated yields.

APA, Harvard, Vancouver, ISO, and other styles

29

El Arba, Marie, Sara E. Dibrell, Frederick Meece, and Doug E. Frantz. "Ru(II)-Catalyzed Synthesis of Substituted Furans and Their Conversion to Butenolides." Organic Letters 20, no. 18 (2018): 5886–88. http://dx.doi.org/10.1021/acs.orglett.8b02554.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Song, Zhi Zhong, Mei Sing Ho, and Henry N. C. Wong. "Regiospecific synthesis of 3,4-disubstituted furans. 7. Synthesis and reactions of 3,4-bis(trimethylsilyl)furan: Diels-Alder cycloaddition, Friedel-Crafts acylation, and regiospecific conversion to 3,4-disubstituted furans." Journal of Organic Chemistry 59, no. 14 (1994): 3917–26. http://dx.doi.org/10.1021/jo00093a025.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Song, Zhi Zhong, Zhong Yuan Zhou, Thomas C. W. Mak, and Henry N. C. Wong. "Regiospecific Conversion of 3,4-Bis(trimethylsilyl)furan to 3,4-Disubstituted Furans: A Novel Suzuki-Type Cross-Coupling of Boroxines." Angewandte Chemie International Edition in English 32, no. 3 (1993): 432–34. http://dx.doi.org/10.1002/anie.199304321.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Tao, Furong, Huanling Song, and Lingjun Chou. "Efficient conversion of cellulose into furans catalyzed by metal ions in ionic liquids." Journal of Molecular Catalysis A: Chemical 357 (May 2012): 11–18. http://dx.doi.org/10.1016/j.molcata.2012.01.010.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Luo, Jia, Yong Xu, Lingjie Zhao, et al. "Two-step hydrothermal conversion of Pubescens to obtain furans and phenol compounds separately." Bioresource Technology 101, no. 22 (2010): 8873–80. http://dx.doi.org/10.1016/j.biortech.2010.06.097.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

MARSHALL, J. A., and G. S. BARTLEY. "ChemInform Abstract: Observations Regarding the Ag(I)-Catalyzed Conversion of Allenones to Furans." ChemInform 26, no. 23 (2010): no. http://dx.doi.org/10.1002/chin.199523108.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Karod, Madeline, Zoe A. Pollard, Maisha T. Ahmad, Guolan Dou, Lihui Gao, and Jillian L. Goldfarb. "Impact of Bentonite Clay on In Situ Pyrolysis vs. Hydrothermal Carbonization of Avocado Pit Biomass." Catalysts 12, no. 6 (2022): 655. http://dx.doi.org/10.3390/catal12060655.

Full text

Abstract:

Biofuels produced via thermochemical conversions of waste biomass could be sustainable alternatives to fossil fuels but currently require costly downstream upgrading to be used in existing infrastructure. In this work, we explore how a low-cost, abundant clay mineral, bentonite, could serve as an in situ heterogeneous catalyst for two different thermochemical conversion processes: pyrolysis and hydrothermal carbonization (HTC). Avocado pits were combined with 20 wt% bentonite clay and were pyrolyzed at 600 °C and hydrothermally carbonized at 250 °C, commonly used conditions across the literatu

APA, Harvard, Vancouver, ISO, and other styles

36

SONG, Z. Z., M. S. HO, and H. N. C. WONG. "ChemInform Abstract: Regiospecific Synthesis of 3,4-Disubstituted Furans. Part 7. Synthesis and Reactions of 3,4-Bis(trimethylsilyl)furan: Diels-Alder Cycloaddition, Friedel-Crafts Acylation, and Regiospecific Conversion to 3,4-Disubstituted Furans." ChemInform 26, no. 1 (2010): no. http://dx.doi.org/10.1002/chin.199501136.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Wanjala, George W., Arnold N. Onyango, David Abuga, Calvin Onyango, and Moses Makayoto. "Does lysine drive the conversion of fatty acid hydroperoxides to aldehydes and alkyl-furans?" Scientific African 12 (July 2021): e00797. http://dx.doi.org/10.1016/j.sciaf.2021.e00797.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Tiecco, Marcello, Lorenzo Testaferri, Marco Tingoli та Francesca Marini. "Selenium Promoted Conversion of α-Substituted β,γ-Unsaturated Ketones into 2,3,5-Trisubstituted Furans". Synlett 1994, № 05 (1994): 373–74. http://dx.doi.org/10.1055/s-1994-22859.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Lee, Phil Ho, Jong Soon Kim, Youn Chul Kim, and Sunggak Kim. "A facile preparation of highly functionalized cyclopropanes and their conversion to cyclopentanones and furans." Tetrahedron Letters 34, no. 47 (1993): 7583–86. http://dx.doi.org/10.1016/s0040-4039(00)60406-9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Ronaghi, Nima, David M. Fialho, Christopher W. Jones, and Stefan France. "Conversion of Unprotected Aldose Sugars to Polyhydroxyalkyl and C-Glycosyl Furans via Zirconium Catalysis." Journal of Organic Chemistry 85, no. 23 (2020): 15337–46. http://dx.doi.org/10.1021/acs.joc.0c02176.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Mettler, Matthew S., Samir H. Mushrif, Alex D. Paulsen, Ashay D. Javadekar, Dionisios G. Vlachos, and Paul J. Dauenhauer. "Revealing pyrolysis chemistry for biofuels production: Conversion of cellulose to furans and small oxygenates." Energy Environ. Sci. 5, no. 1 (2012): 5414–24. http://dx.doi.org/10.1039/c1ee02743c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Patil, Santoshkumar N., and Fei Liu. "Base-Assisted Regio- and Diastereoselective Conversion of Functionalized Furans to Butenolides Using Singlet Oxygen." Organic Letters 9, no. 2 (2007): 195–98. http://dx.doi.org/10.1021/ol062551l.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Galadima, Ahmad, and Oki Muraza. "Zeolite catalyst design for the conversion of glucose to furans and other renewable fuels." Fuel 258 (December 2019): 115851. http://dx.doi.org/10.1016/j.fuel.2019.115851.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Romo, Joelle E., Nathan V. Bollar, Coy J. Zimmermann, and Stephanie G. Wettstein. "Conversion of Sugars and Biomass to Furans Using Heterogeneous Catalysts in Biphasic Solvent Systems." ChemCatChem 10, no. 21 (2018): 4805–16. http://dx.doi.org/10.1002/cctc.201800926.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Chang, Chu-An, Stefan Gürtzgen, Erik P. Johnson та K. Peter C. Vollhardt. "Stoichiometric and Catalytic (η 5-Cyclopentadienyl)cobalt-Mediated Cycloisomerizations of Ene-Yne-Ene Type Allyl Propargyl Ethers". Synthesis 52, № 03 (2019): 399–416. http://dx.doi.org/10.1055/s-0039-1690727.

Full text

Abstract:

The complexes CpCoL2 (Cp = C5H5; L = CO or CH2=CH2) mediate the cycloisomerizations of α,δ,ω-enynenes containing allylic ether linkages to 3-(oxacyclopentyl or cycloalkyl)furans via the intermediacy of isolable CpCo-η 4-dienes. A suggested mechanism comprises initial complexation of the triple bond and one of the double bonds, then oxidative coupling to a cobalt-2-cyclopentene, terminal double bond insertion to assemble a cobalta-4-cycloheptene, β-hydride elimination, and reductive elimination to furnish a CpCo-η 4-diene. When possible, the cascade continues through cobalt-mediated hydride shi

APA, Harvard, Vancouver, ISO, and other styles

46

Van Nguyen, Chi, Jing Rou Boo, Chia-Hung Liu, et al. "Oxidation of biomass-derived furans to maleic acid over nitrogen-doped carbon catalysts under acid-free conditions." Catalysis Science & Technology 10, no. 5 (2020): 1498–506. http://dx.doi.org/10.1039/c9cy02364j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Kannan, P., G. Lakshmanan, A. Al Shoaibi, and C. Srinivasakannan. "Equilibrium model analysis of waste plastics gasification using CO2 and steam." Waste Management & Research: The Journal for a Sustainable Circular Economy 35, no. 12 (2017): 1247–53. http://dx.doi.org/10.1177/0734242x17736946.

Full text

Abstract:

Utilization of carbon dioxide (CO2) in thermochemical treatment of waste plastics may significantly help to improve CO2 recycling, thus simultaneously curtailing dioxins/furans and CO2 emissions. Although CO2 is not such an effective gasifying agent as steam, a few investigations have explored the utilization of CO2 in conjunction with steam to achieve somewhat higher carbon conversion. This work presents a comparative evaluation study of CO2 and steam gasification of a typical post-consumer waste plastics mixture using an Aspen Plus equilibrium model. The effect of flow rate of gasifying medi

APA, Harvard, Vancouver, ISO, and other styles

48

Patil, Santoshkumar N., та Fei Liu. "Fluoride-Assisted Regioselective Conversion of Functionalized Furans to α-Substituted γ-Hydroxybutenolides Using Singlet Oxygen". Journal of Organic Chemistry 72, № 16 (2007): 6305–8. http://dx.doi.org/10.1021/jo070666c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Nikbin, Nima, Stavros Caratzoulas, and Dionisios G. Vlachos. "On the oligomerization mechanism of Brønsted acid-catalyzed conversion of furans to diesel-range fuels." Applied Catalysis A: General 485 (September 2014): 118–22. http://dx.doi.org/10.1016/j.apcata.2014.07.035.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Kopytko, Ya F. "Quantitative Determination of Total Carbohydrates (Recalculated for Fructose After Conversion to Furans) in Burdock Juice." Pharmaceutical Chemistry Journal 51, no. 4 (2017): 285–87. http://dx.doi.org/10.1007/s11094-017-1599-y.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!