Relevant bibliographies by topics / N,N'-dicyclohexylcarbodiimide

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'N,N'-dicyclohexylcarbodiimide'

Author: Grafiati
Published: 28 May 2022
Last updated: 31 July 2025

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Journal articles on the topic "N,N'-dicyclohexylcarbodiimide"

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

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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6

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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7

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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8

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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9

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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10

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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Dissertations / Theses on the topic "N,N'-dicyclohexylcarbodiimide"

1

Varvarenko, S. M., N. V. Puzko, A. S. Voronov, et al. "Colloidal and Chemical Properties of Polyesters Based on Glutamic Acid and Diols of Different Nature." Thesis, Sumy State University, 2012. http://essuir.sumdu.edu.ua/handle/123456789/35074.

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The paper describes synthesis method and colloid-chemical properties of novel α-amino acid based polyesters with controllable hydrophilic-lipophillic balance. Glutamic acid and diols of different nature based polyesters were obtained via low-temperature activated polyesterefication. Such polymers are able to form micellar structures in self-stabilized water dispersion. Solubilization of water insoluble dyes Sudan and toluene in polymer water solution was studied. Due to micelle forming ability and prognosticated biodegradability to non-toxic products, obtained polymers are promising mater
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Book chapters on the topic "N,N'-dicyclohexylcarbodiimide"

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Heyde, Sandra, and Peter Jahns. "The Influence of N,N’-Dicyclohexylcarbodiimide (DCCD) on the Kinetics and pH-Dependence of Zeaxanthin Formation in Isolated Pea (Pisum sativum) Thylakoids." In Photosynthesis: Mechanisms and Effects. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-3953-3_535.

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Nałȩcz, Maceij J., Robert P. Casey, and Angelo Azzi. "[7] Use of N,N′-dicyclohexylcarbodiimide to study membrane-bound enzymes." In Methods in Enzymology. Elsevier, 1986. http://dx.doi.org/10.1016/s0076-6879(86)25009-0.

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Ho, M. N., and T. H. Stevens. "VMA3." In Secretory Pathway. Oxford University PressOxford, 1994. http://dx.doi.org/10.1093/oso/9780198599425.003.0159.

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Abstract The sequence of the VMA3 gene (GenBank accession #X15155) contains an open reading frame encoding a hydrophobic protein of 160 amino acids with a predicted molecular mass of 16.3 kDa12 The amino acid sequence exhibits 58% identity to the proteolipid of bovine chromaffin granules V-type H+-ATPase and shows similar identity to vacuolar H+-ATPase proteolipids from other organisms. Vma3p is predicted to have four transmembrane spanning regions, however it does not appear to have a cleavable signal sequence12. In addition, Vma3p contains a putative N,N’-dicyclohexylcarbodiimide (DCCD)bindi
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4

Azzi, Angelo, Kristine Sigrist-Nelson, and Nathan Nelson. "[52] Extraction, purification, and reconstruction of the chloroplast N,N′-Dicyclohexylcarbodiimide-binding proteolipid." In Methods in Enzymology. Elsevier, 1986. http://dx.doi.org/10.1016/s0076-6879(86)26054-1.

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Journal articles
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