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Journal articles on the topic 'N'-dicyclohexylcarbodiimide'

Author: Grafiati

Published: 28 May 2022

Last updated: 31 July 2025

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1

Hritzová, Oľga. "Reactions of vinylene diisothiocyanate with aniline, N-benzylidenemethylamine and N,N'-dicyclohexylcarbodiimide." Collection of Czechoslovak Chemical Communications 50, no. 10 (1985): 2170–73. http://dx.doi.org/10.1135/cccc19852170.

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Reaction of vinylene diisothiocyanate with aniline, N-benzylidenemethylamine and N,N'-dicyclohexylcarbodiimide affords the stable 1-(anilinothiocarbonyl)-4-imidazoline-2-thione and 1,3,5-thiadiazine derivatives, respectively.

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2

Grotmol, T., T. Buanes, and M. G. Ræder. "DCCD (N, N′-Dicyclohexylcarbodiimide) Inhibits Biliary Secretion of HCO3." Scandinavian Journal of Gastroenterology 22, no. 2 (1987): 207–13. http://dx.doi.org/10.3109/00365528708991881.

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3

Chowdhry, Babur Z., Trevor J. Dines, Stephen A. Leharne, John P. Ryall, Iqbal T. Shadi, and Robert Withnall. "Vibrational spectroscopy and DFT calculations of N,N′-dicyclohexylcarbodiimide." Journal of Raman Spectroscopy 42, no. 2 (2011): 230–38. http://dx.doi.org/10.1002/jrs.2674.

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4

Chawla, Pooja A., Arshdeep Singh, and Anjali Sharma. "The Catalyst’s Companion: N,N′-Dicyclohexylcarbodiimide (DCC) in Action." SynOpen 07, no. 04 (2023): 562–65. http://dx.doi.org/10.1055/s-0042-1751500.

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5

Sparling, Richard, Michael Blaut, and Gerhard Gottschalk. "Bioenergetic studies of Methanosphaera stadtmanae, an obligate H2–methanol utilising methanogen." Canadian Journal of Microbiology 39, no. 8 (1993): 742–48. http://dx.doi.org/10.1139/m93-109.

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In Methanosphaera stadtmanae producing methane from the reduction of methanol with H2, sodium (> 0.3 mM Na+) was not required for methanogenesis or ATP synthesis. The ATPase inhibitor N,N′-dicyclohexylcarbodiimide inhibited both ATP synthesis and methanogenesis, but was only effective in the presence of low Na+ (< 1 mM). The observed N,N′ -dicyclohexylcarbodiimide inhibition of methanogenesis was relieved by the addition of the protonophore 3,3′,4′,5-tetrachlorosalicylanilide. 3,3′,4′,5-Tetrachlorosalicylanilide itself caused a rapid decrease in the intracellular ATP concentration and st

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6

Vas’kevich, R. I., P. V. Savitskii, Yu L. Zborovskii, and V. I. Staninets. "Reaction of 1-hetaryl-4-phenylthiosemicarbazides with N,N′-dicyclohexylcarbodiimide." Russian Journal of Organic Chemistry 45, no. 9 (2009): 1386–89. http://dx.doi.org/10.1134/s1070428009090127.

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7

Suchi, Raul, Yael Stern-Bach, Tal Gabay, and Shimon Schuldiner. "Covalent modification of the amine transporter with N,N'-dicyclohexylcarbodiimide." Biochemistry 30, no. 26 (1991): 6490–94. http://dx.doi.org/10.1021/bi00240a020.

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8

Geffken, Detlef, and Knuth Strohauer. "3-Substituierte 1-AIkoxyindolin-2-one aus N-Alkoxy-2-phenylgIycoIamiden und Dicyclohexylcarbodiimid / 3-Substituted 1-Alkoxyindolin-2-ones from N-Alkoxy-2-phenylglycolamides and Dicyclohexylcarbodiimide." Zeitschrift für Naturforschung B 40, no. 3 (1985): 398–401. http://dx.doi.org/10.1515/znb-1985-0315.

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9

Rimpiläinen, Marja A. "Properties of the N,N'-dicyclohexylcarbodiimide resistant ATPase OF Streptococcus cremoris." International Journal of Biochemistry 19, no. 8 (1987): 729–32. http://dx.doi.org/10.1016/0020-711x(87)90089-9.

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10

Schneider, Wolfgang, Andreas Bauer, and Hubert Schmidbaur. "[(N, N’, N”-Tricyclohexyl)-N”- cyclohexylcarbamoylguanidinium] Tetrachloroaurate(III) as a Product of the Reaction of Dicyclohexylcarbo- diimide with HAuCl4 . aq." Zeitschrift für Naturforschung B 52, no. 9 (1997): 1152–54. http://dx.doi.org/10.1515/znb-1997-0922.

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Reaction of tetrachloroauric(III) acid hydrate with dicyclohexylcarbodiimide (dcc) in dichloromethane in the presence of equimolar amounts of triethylamine leads to a complex reaction mixture. One of the components was shown by X-ray crystallography to be [(N, N’, N”-tricyclohexyl)- N”-cyclohexylcarbamoylguanidinium] tetrachloroaurate( III) (1) which contains as a cation the addition product of dcc with the corresponding urea.

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11

Fairushina, A. I., S. F. Petrova, and L. A. Baltina. "Selective Synthesis of Amino Acid Conjugates of Glycyrrhizic Acid Using N-Oxyphthalimide and N,N′-Dicyclohexylcarbodiimide." Žurnal obŝej himii 94, no. 7 (2024): 815–22. https://doi.org/10.31857/s0044460x24070035.

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A selective synthesis of amino acid conjugates of glycyrrhizic acid containing amino acid residues in the carbohydrate part of the glycoside was proposed using N-oxyphthalimide (HOPt) and N,N′-dicyclohexylcarbodiimide (DCC), tert-butyl and benzyl/4-nitrobenzyl esters of L-amino acids with yields of 55–60%. Free conjugates of glycyrrhizic acid with valine, isoleucine, methionine, phenylalanine, leucine, tyrosine and glutamic acid were obtained by deblocking the ester groups.

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12

Manolov, Stanimir, Iliyan Ivanov, and Dimitar Bojilov. "N-(2-(1H-indol-3-yl)ethyl)-2-(6-chloro-9H-carbazol-2-yl)propanamide." Molbank 2020, no. 4 (2020): M1171. http://dx.doi.org/10.3390/m1171.

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The titular compound was prepared by a reaction between tryptamine and carprofen, applying, as a “dehydrating” reagent, N,N’-dicyclohexylcarbodiimide. The newly synthesized compound was fully analyzed and characterized via 1H, 13C-NMR, UV, IR, and mass spectral data.

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13

Sokol, P. P., P. D. Holohan, and C. R. Ross. "N,N'-dicyclohexylcarbodiimide inactivates organic cation transport in renal brush border membranes." Journal of Pharmacology and Experimental Therapeutics 243, no. 2 (1987): 455–59. https://doi.org/10.1016/s0022-3565(25)11005-7.

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14

Igarashi, P., and P. S. Aronson. "Covalent modification of the renal Na+/H+ exchanger by N,N'-dicyclohexylcarbodiimide." Journal of Biological Chemistry 262, no. 2 (1987): 860–68. http://dx.doi.org/10.1016/s0021-9258(19)75866-9.

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15

PALMER, Tracy, Ross WILLIAMS, Nick P. J. COTTON, Christopher M. THOMAS, and J. Baz JACKSON. "Inhibition of proton-translocating transhydrogenase from photosynthetic bacteria by N,N'-dicyclohexylcarbodiimide." European Journal of Biochemistry 211, no. 3 (1993): 663–69. http://dx.doi.org/10.1111/j.1432-1033.1993.tb17594.x.

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16

Takahashi, Takayuki, та Kenji Takahashi. "N,N′-dicyclohexylcarbodiimide is a specific, reversible inhibitor of proline-β-naphthylamidase". Biochemical and Biophysical Research Communications 168, № 3 (1990): 1001–6. http://dx.doi.org/10.1016/0006-291x(90)91128-f.

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17

Soldatova, N. S., K. V. Orlova, and T. A. Sarycheva. "One-Pot Amide Synthesis via Thermal Decomposition N-Acylureas under Microwave Irradiation." Key Engineering Materials 685 (February 2016): 785–88. http://dx.doi.org/10.4028/www.scientific.net/kem.685.785.

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A simple one-pot amidation of carboxylic acids promoted by microwave irradiation is described. Reaction includes formation N-acylureas via interaction carboxylic acids and N,N-dicyclohexylcarbodiimide followed thermal decomposition N-acylureas in microwave reactor. This method allows carrying out the reaction in a short time with good yields.

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18

ŚLEBIODA, MAREK, ZBIGNIEW WODECKI, and ALEKSANDER M. KOŁODZIEJCZYK. "Formation of optically pure N-acyl-N,N′-dicyclohexylurea in N,N′-dicyclohexylcarbodiimide-mediated peptide synthesis." International Journal of Peptide and Protein Research 35, no. 6 (2009): 539–41. http://dx.doi.org/10.1111/j.1399-3011.1990.tb00258.x.

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19

Geffken, Detlef, and Knuth Strohauer. "Synthese und Eigenschaften von 4-Alkoxy-4,5-dihydro-2H-thieno[3.2-b]pyrrol-5-onen Synthesis and Properties of 4-Alkoxy-4,5-dihydro-2H-thieno[3.2-b]pyrrole-5-ones / Synthesis and Properties of 4-Alkoxy-4,5-dihydro-2H-thieno[3.2-b]pyrrole-5-ones." Zeitschrift für Naturforschung B 41, no. 1 (1986): 89–92. http://dx.doi.org/10.1515/znb-1986-0119.

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The reaction of (2-thienyl)substituted N-alkoxyglycolam ides (4) with dicyclohexylcarbodiimide at ambient temperature gives 4-alkoxy-4,5-dihydro-2H -thieno[3.2-b]pyrrole-5-ones (5) in moderate yields.

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20

Manolov, Stanimir, Iliyan Ivanov, and Yulian Voynikov. "N-[2-(1H-Indol-3-yl)ethyl]-2-(4-isobutylphenyl)propanamide." Molbank 2018, no. 4 (2018): M1031. http://dx.doi.org/10.3390/m1031.

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The compound in the title was prepared by reaction between tryptamine and ibuprofen using N,N′-dicyclohexylcarbodiimide as a “dehydrating” reagent. The structure of the newly synthesized compound was determined by nuclear magnetic resonance (NMR) (1H-NMR and 13C-NMR), UV, IR, and mass spectral data.

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21

Kaestner, K. H., S. K. Randall, and H. Sze. "N,N'-dicyclohexylcarbodiimide-binding proteolipid of the vacuolar H+-ATPase from oat roots." Journal of Biological Chemistry 263, no. 3 (1988): 1282–87. http://dx.doi.org/10.1016/s0021-9258(19)57297-0.

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22

Aviram, A., and I. Aviram. "Activation of guinea-pig and bovine neutrophil NADPH oxidase by N,N′-dicyclohexylcarbodiimide." Biochimica et Biophysica Acta (BBA) - Molecular Cell Research 844, no. 2 (1985): 224–32. http://dx.doi.org/10.1016/0167-4889(85)90094-1.

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23

Baltina, L. A., A. I. Fairushina, and L. A. Baltina. "Synthesis of amino acid conjugates of glycyrrhizic acid using N-hydroxyphthalimide and N,N'-dicyclohexylcarbodiimide." Russian Journal of General Chemistry 85, no. 12 (2015): 2735–38. http://dx.doi.org/10.1134/s1070363215120129.

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24

Fang, Weihuan, Henrik Siegumfeldt, Birgitte Bjørn Budde, and Mogens Jakobsen. "Osmotic Stress Leads to Decreased Intracellular pH of Listeria monocytogenes as Determined by Fluorescence Ratio-Imaging Microscopy." Applied and Environmental Microbiology 70, no. 5 (2004): 3176–79. http://dx.doi.org/10.1128/aem.70.5.3176-3179.2004.

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ABSTRACT Intracellular pH (pHi) of Listeria monocytogenes was determined after exposure to NaCl or sorbitol in liquid and solid media (agar). Both compounds decreased pHi, and recovery on solid medium was impaired compared to that in liquid medium. N,N′-dicyclohexylcarbodiimide abolished pHi recovery, and lowering aw with glycerol showed no effect on pHi.

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25

Wang, Yan Mei, Atsushi Ikeda, Naruhito Hori, et al. "N,N-dicyclohexylcarbodiimide assisted synthesis and characterization of poly(vinyl alcohol-co-vinyl levulinate)." Polymer 46, no. 23 (2005): 9793–802. http://dx.doi.org/10.1016/j.polymer.2005.07.088.

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26

Belcheva, Nadya, Ivan M. Panayotov та Christo Tsvetanov. "The interaction of alkyl α-(S)-Malates with N,N′-dicyclohexylcarbodiimide under mild conditions". European Polymer Journal 27, № 6 (1991): 479–82. http://dx.doi.org/10.1016/0014-3057(91)90170-s.

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27

Jung, Hyun Jun, and Dong Gun Lee. "Synergistic antibacterial effect between silybin and N,N′-dicyclohexylcarbodiimide in clinical Pseudomonas aeruginosa isolates." Journal of Microbiology 46, no. 4 (2008): 462–67. http://dx.doi.org/10.1007/s12275-008-0138-7.

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28

Sheikhi, Ehsan, Mehdi Adib, Morteza Karajabad, and Seyed Gohari. "Sulfuric Acid-Promoted Oxidation of Benzylic Alcohols to Aromatic Aldehydes in Dimethyl Sulfoxide: An Efficient Metal-Free Oxidation Approach." Synlett 29, no. 07 (2018): 974–78. http://dx.doi.org/10.1055/s-0037-1609149.

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An efficient metal-free oxidation of benzylic alcohols to aromatic aldehydes is described. Heating a solution of the benzylic alcohol in DMSO in the presence of H2SO4 afforded the corresponding aldehyde in excellent yield. This oxidation reaction, which proceeds with a short reaction time and no side products, is akin to the Pfitzner–Moffatt oxidation, but without the need for N,N′-dicyclohexylcarbodiimide.

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29

KASTURl, LAL, LAL KOLEY PANNA, and RAY SUPRABHAT. "Amino Acid Esters of Norethindrone as Possible Acrosin Inhibitors." Journal of Indian Chemical Society Vol. 63, Apr 1986 (1986): 432–34. https://doi.org/10.5281/zenodo.6274516.

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Medicinal Chemistry Division, Central Drug Research Institute, Lucknow-226 001 Manuscript <em>received 10 October 1985, accepted 17 February 1986</em> A series of amino acid esters of norethindrone (I) have been synthesised as possible acrosin inhibitors by reacting different amino acids with I in the presence of equimolar amounts of 4-<em>N,N</em>-diaethylaminopyridine (DMAP) and dicyclohexylcarbodiimide (DCC).

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30

Toei, Masashi, and Hiroyuki Noji. "Single-molecule Analysis of F0F1-ATP Synthase Inhibited byN,N-Dicyclohexylcarbodiimide." Journal of Biological Chemistry 288, no. 36 (2013): 25717–26. http://dx.doi.org/10.1074/jbc.m113.482455.

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31

Manolov, Stanimir, Iliyan Ivanov, and Dimitar Bojilov. "N-(2-(1H-indol-3-yl)ethyl)-2-(2-fluoro-[1,1′-biphenyl]-4-yl)propanamide." Molbank 2021, no. 1 (2020): M1177. http://dx.doi.org/10.3390/m1177.

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N-(2-(1H-Indol-3-yl)ethyl)-2-(2-fluoro-[1,1′-biphenyl]-4-yl)propanamide was prepared by a reaction between tryptamine and flurbiprofen, applying N,N’-dicyclohexylcarbodiimide, as a coupling agent. The obtained new amide has a fragment similar to Brequinar, a compound used in SARS-CoV-2 treatment trials. The newly synthesized compound was fully analyzed and characterized via 1H, 13C-NMR, UV, IR, and mass spectral data.

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32

Dutta, Arpita, Suven Das, Purak Das, Suvendu Maity, and Prasanta Ghosh. "Fibril formation through self-assembly of a simple glycine derivative and X-ray diffraction study." Zeitschrift für Kristallographie - Crystalline Materials 235, no. 1-2 (2020): 47–51. http://dx.doi.org/10.1515/zkri-2019-0062.

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AbstractN-(N-benzoyl glycinyl)-N,N′-dicyclohexylurea was synthesised by conjugating N-benzoyl glycine and dicyclohexylcarbodiimide (DCC) using triethylamine as base catalyst. A single crystal X-ray diffraction study reveals that the compound self-assembles into a supramolecular sheet structure by intermolecular N–H · · · O, C–H · · · O hydrogen bonding and non-bonding van der Waals interactions. A high resolution transmission electronic microscopic (HR-TEM) image of the compound exhibits formation of fibrils in the solid state.

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33

Hejsek, Miloslav, Jan Slouka, Vojtěch Bekárek, and Antonín Lyčka. "Cyclization Reactions of 2-(6-Azauracil-5-yl)benzoic Acid and Some Its Derivatives." Collection of Czechoslovak Chemical Communications 57, no. 1 (1992): 123–33. http://dx.doi.org/10.1135/cccc19920123.

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2-(6-Azauracil-5-yl)benzoic acid (Ib) and its thio analogue Ia give new heterocyclic compounds, 1,2-dihydro-1,2,4-triazino[5,6-c]isocoumarin-3-one (IVb) and analogous 3-thione IVa, respectively, on treatment with N,N'-dicyclohexylcarbodiimide. A series of substituted 1,2,4-triazino[5,6-c]isoquinolines V-XVI have been prepared from these compounds and from other functional derivatives (II, III) of the acids I.

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34

Li, Ning, Yuan Huang, Wan Xiao, Xian Li, Pingya Li, and Jinping Liu. "Synthesis and Cytotoxic Activities of New Fatty Acid Esters of 20(S)-Protopanaxadiol." Zeitschrift für Naturforschung C 66, no. 5-6 (2011): 199–204. http://dx.doi.org/10.1515/znc-2011-5-601.

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In order to find new lead compounds with antitumour activies, thirteen new fatty acid esters of 20(S)-protopanaxadiol (PPD) were synthesized using oleoyl chloride or fatty acids and N,N’-dicyclohexylcarbodiimide (DCC). Their cytotoxic activities were tested using the MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] method, and the structure- activity relationships between the fatty acid esters of PPD and their cytotoxic activities are discussed.

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35

Rea, P. A., C. J. Griffith, and D. Sanders. "Purification of the N,N'-dicyclohexylcarbodiimide-binding proteolipid of a higher plant tonoplast H+-ATPase." Journal of Biological Chemistry 262, no. 30 (1987): 14745–52. http://dx.doi.org/10.1016/s0021-9258(18)47858-1.

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36

Pringle, Michael J., and Magdalena Taber. "Fluorescent analogs of N,N'-dicyclohexylcarbodiimide as structural probes of the bovine mitochondrial proton channel." Biochemistry 24, no. 25 (1985): 7366–71. http://dx.doi.org/10.1021/bi00346a051.

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37

Huang, Chao, Zhi-Gang Qian, and Jian-Jiang Zhong. "Enhancement of ginsenoside biosynthesis in cell cultures of Panax ginseng by N,N′-dicyclohexylcarbodiimide elicitation." Journal of Biotechnology 165, no. 1 (2013): 30–36. http://dx.doi.org/10.1016/j.jbiotec.2013.02.012.

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38

Friedrich, Thomas, Jutta Sablotni, and Gerhard Burckhardt. "Identification of the renal Na+/H+ exchanger with N,N′-dicyclohexylcarbodiimide (DCCD) and amiloride analogues." Journal of Membrane Biology 94, no. 3 (1986): 253–66. http://dx.doi.org/10.1007/bf01869721.

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39

Nováková, Z., S. Šurín, J. Blaško, A. Majerník, and P. Šmigáň. "Membrane proteins and squalene-hydrosqualene profile in methanoarchaeon Methanothermobacter thermautotrophicus resistant to N,N′-dicyclohexylcarbodiimide." Folia Microbiologica 53, no. 3 (2008): 237–40. http://dx.doi.org/10.1007/s12223-008-0034-x.

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40

Tutacz, Peter, Ronny Syre, Cristian G. Hrib, et al. "The First Aziridinylguanidinates: New Precursors for Potentially Volatile Metal Guanidinates." Australian Journal of Chemistry 67, no. 7 (2014): 1110. http://dx.doi.org/10.1071/ch14228.

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The first lithium-aziridinylamidinates, Li[(C2H4N)C(NR)2]·THF (R = iPr (3), Cy (4); iPr = isopropyl, Cy = cyclohexyl), have been prepared by addition of N-aziridinyllithium, C2H4NLi (2), to either N,N′-diisopropylcarbodiimide or N,N′-dicyclohexylcarbodiimide. The cyclohexyl derivative 4 was crystallised from both diethyl ether (Et2O) and THF to afford the crystalline solvent adducts {Li[(C2H4N)C(NR)2]·S}2 (4: S = THF; 4a: S = Et2O) which were structurally characterised by X-ray diffraction. In the solid state, these lithium-aziridinylamidinates comprise ladder-type dimeric molecular structures

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41

Aly, A. A., H. M. Ammar, and A. A. Khalil. "Copolymerization Parameters of 2-(N-Phthalimido) ethyl Methacrylate with Different Vinyl Monomers." Material Science Research India 8, no. 1 (2011): 17–24. http://dx.doi.org/10.13005/msri/080103.

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2-(N-phthalimido)ethyl methacrylate was prepared by the reaction of methacrylic acid with N-(2-hydroxyethyl)phthalimide in presence of N,N?-dicyclohexylcarbodiimide. The monomer reactivity ratios for copolymerization reactions of 2-(N-phthalimido)ethyl methacrylate with methyl acrylate, ethyl acrylate, butyl acrylate and styrene, respectively, in solution with azobisisobutyronitrile (AIBN) as initiator, were estimated by nitrogen analysis. The structure of the copolymers was investigated by IR spectroscopy. The Q and e values for 2-(N-phthalimido)ethyl methacrylate were calculated. Some of the

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42

Nasrabadi, Fatemeh Zeinali, Ali Ramazani, and Yavar Ahmadi. "Synthesis of sterically congested 1,3,4-oxadiazole derivatives from aromatic carboxylic acids, N,N-dicyclohexylcarbodiimide and (N-isocyanimino)triphenylphosphorane." Molecular Diversity 15, no. 3 (2011): 791–98. http://dx.doi.org/10.1007/s11030-011-9310-9.

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43

Terpstra, W., J. W. J. Lambers, and Y. K. Levine. "Studies on chlorophyllase. II. Interaction of the enzyme with concanavalin A and with N, N'-dicyclohexylcarbodiimide." Photobiochemistry and Photobiophysics 11, no. 4 (1986): 249–55. http://dx.doi.org/10.1016/s0165-8646(24)00540-3.

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44

Mizutani, K., M. Yamamoto, K. Suzuki, et al. "Structure of the rotor ring modified with N,N'-dicyclohexylcarbodiimide of the Na+-transporting vacuolar ATPase." Proceedings of the National Academy of Sciences 108, no. 33 (2011): 13474–79. http://dx.doi.org/10.1073/pnas.1103287108.

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45

Friedrich, Thomas, Jutta Sablotni, and Gerhard Burckhardt. "Inhibition of sodium-dependent transport systems in rat renal brush-border membranes with N,N′-dicyclohexylcarbodiimide." Biochemical and Biophysical Research Communications 147, no. 1 (1987): 375–81. http://dx.doi.org/10.1016/s0006-291x(87)80132-8.

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46

Nyren, Paal, Beston F. Nore, and Aake Strid. "Proton-pumping N,N'-dicyclohexylcarbodiimide-sensitive inorganic: pyrophosphate synthase from Rhodospirillum rubrum: purification, characterization, and reconstitution." Biochemistry 30, no. 11 (1991): 2883–87. http://dx.doi.org/10.1021/bi00225a022.

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47

TRCHOUNIAN, ARMEN A., and ANAIT V. VASSILIAN. "Potassium-Stimulated N,N'-Dicyclohexylcarbodiimide-Sensitive ATPase Activity in the Membranes of Anaerobically Grown Escherichia coli." Annals of the New York Academy of Sciences 671, no. 1 Ion-Motive AT (1992): 490–92. http://dx.doi.org/10.1111/j.1749-6632.1992.tb43838.x.

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48

Griffiths, David, Armelle Buzy, Keith Jennings, Alan Millar, Edward Ryan, and David Palmer. "Electrospray ionisation studies of the interaction of N,N′- dicyclohexylcarbodiimide with ceroid lipofuscinosis protein (subunit c)." European Journal of Mass Spectrometry 3, no. 1 (1997): 81. http://dx.doi.org/10.1255/ejms.5.

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Popova, L. G., D. A. Matalin, and Yu V. Balnokin. "Electrogenesis in Plasma Membrane Fraction of Halotolerant Microalga Dunaliella maritima and Effects of N,N′-Dicyclohexylcarbodiimide." Biochemistry (Moscow) 85, no. 8 (2020): 930–37. http://dx.doi.org/10.1134/s0006297920080088.

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Masuda, K. "Cleavage and isolation of the outer sheath of Treponema phagedenis by treatment with N,N′-dicyclohexylcarbodiimide." FEMS Microbiology Letters 41, no. 1 (1987): 73–78. http://dx.doi.org/10.1016/0378-1097(87)90286-2.

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