Log in

Relevant bibliographies by topics / Cyclodehydration / Journal articles

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

Journal articles on the topic 'Cyclodehydration'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 February 2022

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 'Cyclodehydration.'

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

Sun, Yufeng, Yatao Huang, Minmin Li, Jia Lu, Nuo Jin, and Bei Fan. "Synthesis of cyclic ethers by cyclodehydration of 1, n -diols using heteropoly acids as catalysts." Royal Society Open Science 5, no. 9 (September 2018): 180740. http://dx.doi.org/10.1098/rsos.180740.

Full text

Abstract:

Heteropoly acids were used as catalysts for cyclodehydration of various 1, n -diols. Cyclodehydration of butane-1,4-diol, pentane-1,5-diol and hexane-1,6-diol catalysed by H 3 PW 12 O 40 gave tetrahydrofuran, tetrahydropyran and oxepane, respectively. Cyclodehydration of diethylene glycol, triethylene glycol, diethylene glycol monomethyl ether and polyethylene glycol 200 catalysed by H 3 PW 12 O 40 gave 1,4-dioxane. In particular, cyclodehydration of hexane-1,6-diol gave an excellent yield of oxepane (80%). The selectivity exhibited by the H 3 PW 12 O 40 catalyst was even better than that exhibited by other reported catalyst systems for similar cyclodehydration reactions.

APA, Harvard, Vancouver, ISO, and other styles

2

Ausekle, E., A. Priksane, and A. Zicmanis. "Cyclodehydration of Diols in Acidic Ionic Liquids." Latvian Journal of Chemistry 50, no. 1-2 (January 1, 2011): 139–44. http://dx.doi.org/10.2478/v10161-011-0059-3.

Full text

Abstract:

Cyclodehydration of Diols in Acidic Ionic Liquids In the presence of sulfonic acid group functionalized Bronsted-acidic ionic liquids, cyclodehydration of 1,2-ethanediol and 1,4-butanediol is investigated. The role of structure and catalytic activity of ionic liquids on the formation of cyclic ethers: 1,4-dioxane and tetrahydrofuran - is determined.

APA, Harvard, Vancouver, ISO, and other styles

3

Costa, A., and J. M. Riego. "AlPO4-Al2O3Promoted Cyclodehydration of Diols." Synthetic Communications 17, no. 11 (August 1987): 1373–76. http://dx.doi.org/10.1080/00397918708057759.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Kelly, Brendan D., and Tristan H. Lambert. "Cyclopropenium-Activated Cyclodehydration of Diols." Organic Letters 13, no. 4 (February 18, 2011): 740–43. http://dx.doi.org/10.1021/ol102980t.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Wali, Anil, and S. Muthukumaru Pillai. "Cyclodehydration of Some 1,n-Diols Catalysed by Sulfated Zirconia." Journal of Chemical Research 23, no. 5 (May 1999): 326–27. http://dx.doi.org/10.1177/174751989902300515.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Gruber, Nadia, Jimena E. Díaz, and Liliana R. Orelli. "Synthesis of dihydroquinazolines from 2-aminobenzylamine: N 3 -aryl derivatives with electron-withdrawing groups." Beilstein Journal of Organic Chemistry 14 (September 26, 2018): 2510–19. http://dx.doi.org/10.3762/bjoc.14.227.

Full text

Abstract:

The sequential N-functionalization of 2-aminobenzylamine (2-ABA) followed by cyclodehydration allowed for a straightforward and efficient synthesis of 3,4-dihydroquinazolines with N-aryl substituents bearing electron-withdrawing groups. The sequence involves an initial SNAr displacement, N-acylation and MW-assisted ring closure. Remarkably, the uncatalyzed N-arylation of 2-ABA led to the monosubstitution product using equimolar amounts of both reagents. The individual steps were optimized achieving good to excellent overall yields of the desired heterocycles, avoiding additional protection and deprotection steps. A mechanistic interpretation for the cyclodehydration reaction promoted by trimethylsilyl polyphosphate (PPSE) is also proposed on the basis of literature data and our experimental observations.

APA, Harvard, Vancouver, ISO, and other styles

7

Morris, Joel, Donn G. Wishka, and Yue Fang. "A Cyclodehydration Route to 2-Aminochromones." Synthetic Communications 24, no. 6 (March 1994): 849–58. http://dx.doi.org/10.1080/00397919408011307.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Chan, Hardy Sze On, and J. R. Lusty. "Acid-Catalyzed Cyclodehydration of Quinazolone Prepolymers." Journal of Macromolecular Science, Part A 23, no. 9 (September 1, 1986): 1057–78. http://dx.doi.org/10.1080/00222338608081112.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Ivanov, Daniela, and Mircea Constantinescu. "Computational study of maleamic acid cyclodehydration." Journal of Physical Organic Chemistry 16, no. 6 (2003): 348–54. http://dx.doi.org/10.1002/poc.639.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Bagley, Mark C., Christian Glover, and Duncan Chevis. "Iodine-Catalysed Bohlmann-Rahtz Cyclodehydration Reactions." Synlett, no. 4 (2005): 649–51. http://dx.doi.org/10.1055/s-2005-863712.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

ONO, MACHIKO, REIKO TODORIKI, and SHINZO TAMURA. "Preparation and cyclodehydration of .BETA.-arylaminocrotonaldehyde." CHEMICAL & PHARMACEUTICAL BULLETIN 34, no. 2 (1986): 463–70. http://dx.doi.org/10.1248/cpb.34.463.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Kwon, Yongseok, Junqi Li, Jolene P. Reid, Jennifer M. Crawford, Roxane Jacob, Matthew S. Sigman, F. Dean Toste, and Scott J. Miller. "Disparate Catalytic Scaffolds for Atroposelective Cyclodehydration." Journal of the American Chemical Society 141, no. 16 (March 28, 2019): 6698–705. http://dx.doi.org/10.1021/jacs.9b01911.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Bezouhanova, C. P., and F. A. Jabur. "Selective cyclodehydration of diols on zeolites." Reaction Kinetics & Catalysis Letters 51, no. 1 (November 1993): 177–81. http://dx.doi.org/10.1007/bf02062493.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Ho, Tse-Lok, Wen-Lung Yeh, John Yule, and Hsing-Jang Liu. "Diels–Alder approach to (±)-longifolene: A formal synthesis." Canadian Journal of Chemistry 70, no. 5 (May 1, 1992): 1375–84. http://dx.doi.org/10.1139/v92-176.

Full text

Abstract:

A formal synthesis of longifolene in racemic form is concluded starting from the Diels–Alder reaction of 6,6-di-methylfulvene and maleic anhydride. Key steps are cyclodehydration, conjugate methylation, and ring expansion.

APA, Harvard, Vancouver, ISO, and other styles

15

Ji, Xiao-Ming, Shu-Juan Zhou, Chen-Liang Deng, Fan Chen, and Ri-Yuan Tang. "NH4PF6-promoted cyclodehydration of α-amino carbonyl compounds: efficient synthesis of pyrrolo[3,2,1-ij]quinoline and indole derivatives." RSC Adv. 4, no. 96 (2014): 53837–41. http://dx.doi.org/10.1039/c4ra11168k.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Chen, Zitao, Xiaoyan Wang, Wanfang Lu, and Jian Yu. "Facile Cyclodehydration of α-Aryloxyketones with Zeolites." Synlett 1991, no. 02 (1991): 121–22. http://dx.doi.org/10.1055/s-1991-20651.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Niyogi, Sobhan, Sukumar Maiti, and Basudam Adhikari. "Cyclodehydration of Poly (amic acid) to Polyimide." International Journal of Polymeric Materials 49, no. 3 (May 2001): 323–30. http://dx.doi.org/10.1080/00914030108039783.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Kelly, Brendan D., and Tristan H. Lambert. "ChemInform Abstract: Cyclopropenium-Activated Cyclodehydration of Diols." ChemInform 42, no. 22 (May 5, 2011): no. http://dx.doi.org/10.1002/chin.201122090.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Andrew Hedley, K., and Stephen P. Stanforth. "Cyclodehydration ofN-(2-nitroaryl)-1,2,3,4-tetrahydroisoquinoline derivatives." Journal of Heterocyclic Chemistry 32, no. 2 (March 1995): 529–30. http://dx.doi.org/10.1002/jhet.5570320226.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Onorato, Amber, Christopher Pavlik, Michael A. Invernale, Ian D. Berghorn, Gregory A. Sotzing, Martha D. Morton, and Michael B. Smith. "Polymer-mediated cyclodehydration of alditols and ketohexoses." Carbohydrate Research 346, no. 13 (September 2011): 1662–70. http://dx.doi.org/10.1016/j.carres.2011.04.017.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Likhatchev, D., L. Valle, M. Canseco, R. Salcedo, R. Gaviño, A. Martinez-Richa, L. Alexandrova, and R. Vera-Graziano. "Spontaneous cyclodehydration ofN-(o-aminophenyl) amic acids." Journal of Applied Polymer Science 67, no. 4 (January 24, 1998): 609–19. http://dx.doi.org/10.1002/(sici)1097-4628(19980124)67:4<609::aid-app3>3.0.co;2-c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Kudelko, Agnieszka, Anna Kędzia, and Karolina Jasiak. "An Efficient Synthesis of New 2-Aryl-5-phenylazenyl-1,3,4-oxadiazole Derivatives from N,N'-Diarylcarbonohydrazides." Synlett 29, no. 13 (June 19, 2018): 1745–48. http://dx.doi.org/10.1055/s-0037-1610105.

Full text

Abstract:

A series of new 1,3,4-oxadiazoles conjugated to aromatic substituents by an azo linker was synthesized in a four-step reaction sequence, involving cyclodehydration of a N,N'-diacylhydrazine fragment and dehydrogenation of the neighboring hydrazine fragment of the intermediate N,N'-diarylcarbonohydrazide.

APA, Harvard, Vancouver, ISO, and other styles

23

Yang, Sai, Liu-lan Shen, Yoon-Jung Kim, and Jin-Hyun Jeong. "Effective and novel enantioselective preparation of pyranopyrazoles and pyranocoumarins that is catalyzed by a quinine-derived primary amine." Organic & Biomolecular Chemistry 14, no. 2 (2016): 623–30. http://dx.doi.org/10.1039/c5ob01656h.

Full text

Abstract:

In this study, we executed an effective and novel enantioselective Michael/cyclodehydration sequential reaction between pyrazolin-5-one (or 4-hydroxy-2-pyrone) and chalcones that is catalyzed by a quinine-derived primary amine L7 in the presence of Boc-d-Phg-OH.

APA, Harvard, Vancouver, ISO, and other styles

24

Veeraraghavan Ramachandran, P., and Barnabas Otoo. "Facile synthesis of 1-trifluoromethylalkenes via the decarboxylation of α-trifluoromethyl-β-lactones." Chemical Communications 51, no. 62 (2015): 12388–90. http://dx.doi.org/10.1039/c5cc03230j.

Full text

Abstract:

DCC-mediated cyclodehydration of α-trifluoromethyl-β-hydroxy acids provides α-trifluoromethylated β-lactone intermediates, without loss of stereoselectivity. These lactones undergo facile decarboxylation providing a simple route to obtain both alkyl and aryl 1-trifluoromethyl alkenes in excellent yields and stereoselectivity.

APA, Harvard, Vancouver, ISO, and other styles

25

Wilkerson, Phillip D., Andrew C. Bean, and Chad E. Stephens. "Synthesis of 4H-3-aryl-2-cyano-1,4-benzothiazine 1,1-dioxides for antiviral studies." Heterocyclic Communications 23, no. 2 (April 1, 2017): 101–3. http://dx.doi.org/10.1515/hc-2017-0028.

Full text

Abstract:

Abstract2-Cyano-substituted 1,4-benzothiazine 1,1-dioxides, required for antiviral studies, were prepared by a reductive cyclodehydration of an ortho-nitro sulfone precursor containing a pendant aryl ketone group. The ring-forming reaction also furnishes a non-cyclized benzamide as a major byproduct via an unexpected acyl transfer reaction.

APA, Harvard, Vancouver, ISO, and other styles

26

Kelly, Jeffery W., and Slayton A. Evans. "Regioselective phosphoranylation and cyclodehydration of triols with diethoxytriphenylphosphorane." Journal of the American Chemical Society 108, no. 24 (November 1986): 7681–85. http://dx.doi.org/10.1021/ja00284a036.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Kantin, Grigory, Evgeny Chupakhin, Dmitry Dar'in, and Mikhail Krasavin. "Efficient cyclodehydration of dicarboxylic acids with oxalyl chloride." Tetrahedron Letters 58, no. 32 (August 2017): 3160–63. http://dx.doi.org/10.1016/j.tetlet.2017.06.089.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Faisal, Muhammad, Nobuaki Sato, Armando T. Quitain, Hiroyuki Daimon, and Koichi Fujie. "Hydrolysis and Cyclodehydration of Dipeptide under Hydrothermal Conditions." Industrial & Engineering Chemistry Research 44, no. 15 (July 2005): 5472–77. http://dx.doi.org/10.1021/ie0500568.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Sun, Qi, Run-Tao Li, Shuo Zhao, You Wu, and Tie-Ming Cheng. "Triphenylphosphine–N-Bromosuccinimide Mediated Chemoselective Cyclodehydration of Diols." Synthesis 47, no. 08 (February 10, 2015): 1154–62. http://dx.doi.org/10.1055/s-0034-1380132.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Gebben, B., M. H. V. Mulder, and C. A. Smolders. "The kinetics of the cyclodehydration reaction of polyhydrazides." Makromolekulare Chemie. Macromolecular Symposia 20-21, no. 1 (July 1988): 37–48. http://dx.doi.org/10.1002/masy.19880200109.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Patel, Jagdish M., and Shubhangi S. Soman. "Regioselective cyclodehydration ofortho-hydroxy acetyl aryloxyketones to benzofuran." Journal of Heterocyclic Chemistry 44, no. 4 (July 2007): 945–49. http://dx.doi.org/10.1002/jhet.5570440434.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

MORRIS, J., D. G. WISHKA, and Y. FANG. "ChemInform Abstract: A Cyclodehydration Route to 2-Aminochromones." ChemInform 25, no. 47 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199447159.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Quek, Xian-Yang, Yejun Guan, Rutger A. van Santen, and Emiel J. M. Hensen. "Ionic-Liquid-Stabilized Rhodium Nanoparticles for Citral Cyclodehydration." ChemSusChem 3, no. 11 (August 30, 2010): 1264–67. http://dx.doi.org/10.1002/cssc.201000188.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Kelly, Jeffery W., and Slayton A. Evans. "Bis(neopentyloxy)triphenylphosphorane: a versatile, nonalkylating cyclodehydration reagent." Journal of Organic Chemistry 51, no. 26 (December 1986): 5490–92. http://dx.doi.org/10.1021/jo00376a103.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Nayak, Maloy, Youngeun Jung, and Ikyon Kim. "Syntheses of pterocarpenes and coumestans via regioselective cyclodehydration." Organic & Biomolecular Chemistry 14, no. 34 (2016): 8074–87. http://dx.doi.org/10.1039/c6ob01451h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Likhatchev, D., L. Valle, M. Canseco, R. Salcedo, R. Gaviño, A. Martinez-Richa, L. Alexandrova, and R. Vera-Graziano. "Spontaneous cyclodehydration of N-(o-aminophenyl) amic acids." Journal of Applied Polymer Science 67, no. 4 (January 24, 1998): 609–19. http://dx.doi.org/10.1002/(sici)1097-4628(19980124)67:4<609::aid-app3>3.0.co;2-u.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Kurzer, Frederick, and Jayantilal N. Patel. "Diisophorone and Related Compounds, Part 29. 3-Aminodiisophorane Derivatives." Zeitschrift für Naturforschung B 46, no. 4 (April 1, 1991): 530–40. http://dx.doi.org/10.1515/znb-1991-0416.

Full text

Abstract:

3-Aminodiisophor-2(7)-en-1-ol and homologues are obtained from the readily accessible 3-ketones by reduction of their respective ketoximes, and are characterized as suitable derivatives. The 3-(ω-phenylthioureido) compound undergoes cyclodehydration to a substituted 8,11a-methanocycloocta[d,e][3.1]benzthiazine. The structures of the individual compounds are correlated with their assigned 13C NMR spectra.

APA, Harvard, Vancouver, ISO, and other styles

38

Francis, Raju, Pallepogu Raghavaiah, and Kuruvilla Pius. "Unusual crystal structure ofN-substituted maleamic acid – very strong effect of intramolecular hydrogen bonds." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 70, no. 6 (December 1, 2014): 942–47. http://dx.doi.org/10.1107/s2052520614018952.

Full text

Abstract:

N-Carbamylmaleamic acid (malur) undergoes cyclodehydration under favourable conditions, as expected, to giveN-carbamyl maleimide.N-(Carboxymethyl) maleamic acid (malgly), however, does not undergo a similar cyclization reaction. Strong π bonding between the C and N of the amide group as well as two intramolecular hydrogen bonds makesmalglya planar molecule, as revealed by single-crystal X-ray studies.

APA, Harvard, Vancouver, ISO, and other styles

39

Jacobsen, NW, and AE Philippides. "Heterocyclic Variants of the Purine System. III. Derivatives of Oxazolo[5,4-e]-1,2,4-Triazine and Oxazolo[4,5-e]-1,2,4-Triazine, Two New Heterocyclic Ring Systems." Australian Journal of Chemistry 40, no. 5 (1987): 977. http://dx.doi.org/10.1071/ch9870977.

Full text

Abstract:

Representative derivatives of the [5,4-e] and [4,5-e] oxazolo-1,2,4-triazine ring systems were prepared by cyclodehydration of the respective 5-acylaminotriazin-6-ones and 6-acylaminotriazin-5-ones. 5-Methylthio-3-phenyltriazin-6-amine also gave a 6-anilino derivative of the [5,4-e] series when treated with phenyl isocyanate, but the method was not a successful route to the [4,5-e] series.

APA, Harvard, Vancouver, ISO, and other styles

40

Loughlin, Wendy A., I. Wayan Muderawan, Michelle A. McCleary, Katie E. Volter, and Malcolm D. King. "Studies Towards the Synthesis of Phorbazoles A - D: Formation of the Pyrrole Oxazole Skeleton." Australian Journal of Chemistry 52, no. 3 (1999): 231. http://dx.doi.org/10.1071/c98169.

Full text

Abstract:

Synthetic approaches towards the synthesis of the pyrrole oxazole skeleton of phorbazoles A–D are described. An efficient synthesis of the pyrrole oxazole skeleton (19) from pyrrole and 4- methoxyacetophenone was developed. In the key step, cyclodehydration of the amide (16) resulted in formation of the diprotected pyrrole oxazole (17). Subsequent deprotection of the diprotected pyrrole oxazole (17) gave the target phorbazole skeleton (19).

APA, Harvard, Vancouver, ISO, and other styles

41

Tka, Najeh, Mohamed Adnene Hadj Ayed, Mourad Ben Braiek, Mahjoub Jabli, and Peter Langer. "Synthesis and investigation on optical and electrochemical properties of 2,4-diaryl-9-chloro-5,6,7,8-tetrahydroacridines." Beilstein Journal of Organic Chemistry 17 (September 20, 2021): 2450–61. http://dx.doi.org/10.3762/bjoc.17.162.

Full text

Abstract:

A facile synthesis of 2,4-diaryl-9-chloro-5,6,7,8-tetrahydroacridine derivatives is reported which is based on POCl3-mediated cyclodehydration followed by double Suzuki–Miyaura cross-coupling. The absorption and fluorescence properties of the obtained products were investigated and their HOMO/LUMO energy levels were estimated by cyclic voltammetry measurements. Besides, density functional theory calculations were carried out for further exploration of their electronic properties.

APA, Harvard, Vancouver, ISO, and other styles

42

Weissman, Steven A., Kai Rossen, and Paul J. Reider. "Stereoselective Synthesis of Styrene Oxides via a Mitsunobu Cyclodehydration." Organic Letters 7, no. 13 (June 2005): 2803. http://dx.doi.org/10.1021/ol051014i.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Gamedze, Makhosazana P., and Comfort M. Nkambule. "Dibutyltin oxide mediated diastereoselective cyclodehydration/sulfonylation of 1,2,4-triols." Tetrahedron Letters 56, no. 14 (April 2015): 1825–29. http://dx.doi.org/10.1016/j.tetlet.2015.02.083.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Filippi, Jean-Jacques, Elisabet Duñach, Xavier Fernandez, and Uwe J. Meierhenrich. "Stereospecific cyclodehydration of 1,4-sulfanylalcohols to thiolanes: mechanistic insights." Tetrahedron 64, no. 42 (October 2008): 9999–10003. http://dx.doi.org/10.1016/j.tet.2008.07.088.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Klimenkovs, Igors, Eduards Bakis, and Anda Priksane. "Propanephosphonic Acid Anhydride–Mediated Cyclodehydration of Maleic Acid Monoamides." Synthetic Communications 43, no. 19 (June 26, 2013): 2634–40. http://dx.doi.org/10.1080/00397911.2012.727060.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Constantinescu, Mircea, and Daniela Ivanov. "Computational study of maleamic acid cyclodehydration with acetic anhydride." International Journal of Quantum Chemistry 106, no. 6 (2006): 1330–37. http://dx.doi.org/10.1002/qua.20889.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

ONO, MACHIKO, REIKO TODORIKI, and SHINZO TAMURA. "A kinetic study of cyclodehydration of .BETA.-arylaminocrotonaldehyde derivatives." CHEMICAL & PHARMACEUTICAL BULLETIN 34, no. 4 (1986): 1468–72. http://dx.doi.org/10.1248/cpb.34.1468.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Weissman, Steven A., Kai Rossen, and Paul J. Reider. "Stereoselective Synthesis of Styrene Oxides via a Mitsunobu Cyclodehydration." Organic Letters 3, no. 16 (August 2001): 2513–15. http://dx.doi.org/10.1021/ol016167u.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Hwang, Soonho, Heemin Park, Yongseok Kwon, and Sanghee Kim. "Acid promoted cyclodehydration of amino alcohols with amide acetal." RSC Adv. 4, no. 104 (2014): 60017–24. http://dx.doi.org/10.1039/c4ra10625c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Sun, Daolai, Junjie Wang, Yasuhiro Yamada, and Satoshi Sato. "Cyclodehydration of diethylene glycol over Ag-modified Al2O3 catalyst." Applied Catalysis A: General 505 (September 2015): 422–30. http://dx.doi.org/10.1016/j.apcata.2015.03.047.

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!