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Journal articles on the topic 'FMOC'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Dolphin, C. T., E. A. Shephard, S. Povey, R. L. Smith, and I. R. Phillips. "Cloning, primary sequence and chromosomal localization of human FMO2, a new member of the flavin-containing mono-oxygenase family." Biochemical Journal 287, no. 1 (1992): 261–67. http://dx.doi.org/10.1042/bj2870261.

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We have previously reported the cloning of cDNAs for a flavin-containing mono-oxygenase (FMO) of man, designated FMO1 [Dolphin, Shephard, Povey, Palmer, Ziegler, Ayesh, Smith & Phillips (1991) J. Biol. Chem. 266, 12379-12385], that is the orthologue of pig and rabbit hepatic FMOs. We now describe the isolation and characterization of cDNA clones for a second human FMO, which we have designated FMO2. The polypeptide encoded by the cDNAs is 558 amino acid residues long, has a calculated M(r) of 63337, and contains putative FAD- and NADP-binding sites that align exactly with those described i

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2

Obkircher, Markus, Christian Stähelin та Fritz Dick. "Formation of Fmoc–β-alanine during Fmoc-protections with Fmoc–OSu". Journal of Peptide Science 14, № 6 (2008): 763–66. http://dx.doi.org/10.1002/psc.1001.

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3

Yoshino, Ryo, Yoshinori Tokairin, Mari Kikuchi, and Hiroyuki Konno. "Fmoc-OPhth, the reagent of Fmoc protection." Tetrahedron Letters 58, no. 16 (2017): 1600–1603. http://dx.doi.org/10.1016/j.tetlet.2017.03.021.

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4

Zou, Yi, Kasra Razmkhah, Nikola P. Chmel, Ian W. Hamley, and Alison Rodger. "Spectroscopic signatures of an Fmoc–tetrapeptide, Fmoc and fluorene." RSC Advances 3, no. 27 (2013): 10854. http://dx.doi.org/10.1039/c3ra41979g.

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5

Adamson, J. Gordon, Mark A. Blaskovich, Hester Groenevelt, and Gilles A. Lajoie. "Simple and convenient synthesis of tert-butyl ethers of Fmoc-serine, Fmoc-threonine, and Fmoc-tyrosine." Journal of Organic Chemistry 56, no. 10 (1991): 3447–49. http://dx.doi.org/10.1021/jo00010a050.

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6

Kumar, Ashish, Anamika Sharma, Elvira Haimov, Ayman El-Faham, Beatriz G. de la Torre, and Fernando Albericio. "Fmoc-Amox, A Suitable Reagent for the Introduction of Fmoc." Organic Process Research & Development 21, no. 10 (2017): 1533–41. http://dx.doi.org/10.1021/acs.oprd.7b00199.

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7

ADAMSON, J. G., M. A. BLASKOVICH, H. GROENEVELT, and G. A. LAJOIE. "ChemInform Abstract: Simple and Convenient Synthesis of tert-Butyl Ethers of Fmoc-Serine, Fmoc-Threonine, and Fmoc-Tyrosine." ChemInform 22, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.199138258.

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8

Wessig, Pablo, Sylvia Czapla, Kristian Möllnitz, and Jutta Schwarz. "Mio- and Dio-Fmoc - Two Modified Fmoc Protecting Groups Promoting Solubility." Synlett 2006, no. 14 (2006): 2235–38. http://dx.doi.org/10.1055/s-2006-949632.

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9

Szczepańska, Elżbieta, Beata Grobelna, Jacek Ryl, Amanda Kulpa, Tadeusz Ossowski, and Paweł Niedziałkowski. "Efficient Method for the Concentration Determination of Fmoc Groups Incorporated in the Core-Shell Materials by Fmoc–Glycine." Molecules 25, no. 17 (2020): 3983. http://dx.doi.org/10.3390/molecules25173983.

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In this paper, we described the synthesis procedure of TiO2@SiO2 core-shell modified with 3-(aminopropyl)trimethoxysilane (APTMS). The chemical attachment of Fmoc–glycine (Fmoc–Gly–OH) at the surface of the core-shell structure was performed to determine the amount of active amino groups on the basis of the amount of Fmoc group calculation. We characterized nanostructures using various methods: transmission electron microscope (TEM), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS) to

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10

Zanna, Nicola, Debora Iaculli, and Claudia Tomasini. "The effect ofl-DOPA hydroxyl groups on the formation of supramolecular hydrogels." Organic & Biomolecular Chemistry 15, no. 27 (2017): 5797–804. http://dx.doi.org/10.1039/c7ob01026e.

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Fmoc-l-DOPA-d-Oxd-OH was prepared starting from commercially availablel-DOPA. Its gelation ability was tested by comparison with Fmoc-l-Tyr-d-Oxd-OH and Fmoc-l-Phe-d-Oxd-OH using ten different triggers.

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11

Haiouani, Kheira, Xingpeng Chen, and Jiaxi Xu. "Expeditious Preparation of N-Fmoc 2-Aminoethanesulfonyl Chlorides with Functionalized 1-Substituents." Current Organic Synthesis 15, no. 2 (2018): 246–55. http://dx.doi.org/10.2174/1570179414666170821120705.

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Aim and Objective: [(9H-Fluoren-9-yl)methoxy]carbonyl (Fmoc)-protected 2-aminoethanesulfonyl chlorides with various functionalized 1-substituents may be of use as building blocks for the Fmoc strategic synthesis of sulfonopeptides. Materials and Method: Fmoc-protected 2-aminoethanesulfonyl chlorides with different functionalized 1- substituents were synthesized via radical addition of N-Fmoc allylamine and xanthates with functionalized Ssubstituents, and subsequent oxidative chlorination with N-chlorosuccimide/HCl. Results: Fmoc-protected 2-aminoethanesulfonyl chlorides with different function

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12

Milton, R. C. deL, E. Becker, S. C. F. Milton, J. E. J. Baxter, and J. F. Elsworth. "Letter to the editor. Improved purities for Fmoc-amino acids from Fmoc-ONSu." International Journal of Peptide and Protein Research 30, no. 3 (2009): 431–32. http://dx.doi.org/10.1111/j.1399-3011.1987.tb03351.x.

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13

Di Gioia, Maria Luisa, Antonella Leggio, Adolfo Le Pera, et al. "Synthesis of Chiral Nitrones from N‐Fmoc Amino Acids and N‐Fmoc Dipeptides." Synthetic Communications 34, no. 18 (2004): 3325–34. http://dx.doi.org/10.1081/scc-200030575.

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14

Lobo-Ruiz, Ariadna, and Judit Tulla-Puche. "General Fmoc-Based Solid-Phase Synthesis of Complex Depsipeptides Circumventing Problematic Fmoc Removal." European Journal of Organic Chemistry 2020, no. 2 (2020): 183–92. http://dx.doi.org/10.1002/ejoc.201901459.

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15

Henczi, Maria, та Donald F. Weaver. "AN IMPROVED SYNTHESIS OF N∊-FMOC-L-LYSINE AND Nδ-FMOC-L-ORNITHINE". Organic Preparations and Procedures International 26, № 5 (1994): 578–80. http://dx.doi.org/10.1080/00304949409458061.

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16

BARLOS, KLEOMENIS, DIMITRIOS GATOS, and SOFIA KOUTSOGIANNI. "Fmoc/Trt-amino acids: comparison to Fmoc/tBu-amino acids in peptide synthesis." Journal of Peptide Research 51, no. 3 (2009): 194–200. http://dx.doi.org/10.1111/j.1399-3011.1998.tb01216.x.

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17

Hasegawa, Koki, Yin Lin Sha, Jeong Kyu Bang, Toru Kawakami, Kenichi Akaji, and Saburo Aimoto. "Preparation of phosphopeptide thioesters by Fmoc-and Fmoc(2-F)-solid phase synthesis." Letters in Peptide Science 8, no. 3-5 (2001): 277–84. http://dx.doi.org/10.1007/bf02446529.

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18

Mourtas, Spyridon, Christina Katakalou, Dimitrios Gatos, and Kleomenis Barlos. "Convergent Synthesis of Thioether Containing Peptides." Molecules 25, no. 1 (2020): 218. http://dx.doi.org/10.3390/molecules25010218.

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Thioether containing peptides were obtained following three synthetic routes. In route A, halo acids esterified on 2-chlorotrityl(Cltr) resin were reacted with N-fluorenylmethoxycarbonyl (Fmoc) aminothiols. These were either cleaved from the resin to the corresponding (Fmoc-aminothiol)carboxylic acids, which were used as key building blocks in solid phase peptide synthesis (SPPS), or the N-Fmoc group was deprotected and peptide chains were elongated by standard SPPS. The obtained N-Fmoc protected thioether containing peptides were then condensed either in solution, or on solid support, with th

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19

Choe, Ranjoo, and Seok Il Yun. "Fmoc-diphenylalanine-based hydrogels as a potential carrier for drug delivery." e-Polymers 20, no. 1 (2020): 458–68. http://dx.doi.org/10.1515/epoly-2020-0050.

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AbstractSelf-assembled hydrogels from 9-fluorenylmethoxycarbonyl-modified diphenylalanine (Fmoc-FF) peptides were evaluated as potential vehicles for drug delivery. During self-assembly of Fmoc-FF, high concentrations of indomethacin (IDM) drugs were shown to be incorporated into the hydrogels. The β-sheet arrangement of peptides was found to be predominant in Fmoc-FF–IDM hydrogels regardless of the IDM content. The release mechanism for IDM displayed a biphasic profile comprising an initial hydrogel erosion-dominated stage followed by the diffusion-controlled stage. Small amounts of polyamido

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20

Fichman, Galit, Tom Guterman, Lihi Adler-Abramovich, and Ehud Gazit. "Synergetic functional properties of two-component single amino acid-based hydrogels." CrystEngComm 17, no. 42 (2015): 8105–12. http://dx.doi.org/10.1039/c5ce01051a.

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21

Hlebowicz, E., A. J. Andersen, L. Andersson та B. A. Moss. "Identification of Fmoc-β-Ala-OH and Fmoc-β-Ala-amino acid-OH as new impurities in Fmoc-protected amino acid derivatives*". Journal of Peptide Research 65, № 1 (2008): 90–97. http://dx.doi.org/10.1111/j.1399-3011.2004.00201.x.

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22

Roy, Karabi, Suvankar Ghosh, Monikha Chetia, Priyadarshi Satpati, and Sunanda Chatterjee. "Dicyclohexylurea derivatives of amino acids as dye absorbent organogels and anion sensors." Organic & Biomolecular Chemistry 17, no. 11 (2019): 3026–39. http://dx.doi.org/10.1039/c9ob00014c.

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Dicyclohexyl urea (DCU) derivatives of amino acids Fmoc-Phe-DCU (M1), Fmoc-Phg-DCU (M2) and Fmoc-Gaba-DCU (M3) have been shown to form phase selective, thermoreversible and mechanically robust gels in a large range of organic solvents. Organogels act as dye adsorbants and M1–M3 act as selective anion sensors for F<sup>−</sup>, OH<sup>−</sup> and OAc<sup>−</sup>.

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23

Liyanage, Wathsala, Kanika Vats, Annada Rajbhandary, Danielle S. W. Benoit, and Bradley L. Nilsson. "Multicomponent dipeptide hydrogels as extracellular matrix-mimetic scaffolds for cell culture applications." Chemical Communications 51, no. 56 (2015): 11260–63. http://dx.doi.org/10.1039/c5cc03162a.

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24

Gahane, Avinash Yashwant, Virender Singh, Ashok Kumar, and Ashwani Kumar Thakur. "Development of mechanism-based antibacterial synergy between Fmoc-phenylalanine hydrogel and aztreonam." Biomaterials Science 8, no. 7 (2020): 1996–2006. http://dx.doi.org/10.1039/c9bm01978b.

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25

J. Stephenson, Rachel, Paul G. Plieger, and David R.K. Harding. "Improved Fmoc Synthesis of Bradykinin." Protein & Peptide Letters 18, no. 9 (2011): 952–55. http://dx.doi.org/10.2174/092986611796011509.

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26

WELLINGS, D. A., and E. ATHERTON. "ChemInform Abstract: Standard Fmoc Protocols." ChemInform 29, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.199812282.

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27

Indra, Radek, Petr Pompach, Václav Martínek, et al. "Identification of Human Enzymes Oxidizing the Anti-Thyroid-Cancer Drug Vandetanib and Explanation of the High Efficiency of Cytochrome P450 3A4 in its Oxidation." International Journal of Molecular Sciences 20, no. 14 (2019): 3392. http://dx.doi.org/10.3390/ijms20143392.

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The metabolism of vandetanib, a tyrosine kinase inhibitor used for treatment of symptomatic/progressive medullary thyroid cancer, was studied using human hepatic microsomes, recombinant cytochromes P450 (CYPs) and flavin-containing monooxygenases (FMOs). The role of CYPs and FMOs in the microsomal metabolism of vandetanib to N-desmethylvandetanib and vandetanib-N-oxide was investigated by examining the effects of CYP/FMO inhibitors and by correlating CYP-/FMO-catalytic activities in each microsomal sample with the amounts of N-desmethylvandetanib/vandetanib-N-oxide formed by these samples. CYP

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28

Kaiser, T., G. J. Nicholson, H. J. Kohlbau, and W. Voelter. "Racemization studies of Fmoc-Cys(Trt)-OH during stepwise Fmoc-Solid phase peptide synthesis." Tetrahedron Letters 37, no. 8 (1996): 1187–90. http://dx.doi.org/10.1016/0040-4039(95)02406-9.

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29

Fan, Erkang, and Somnath Mondal. "Mild and Efficient Synthesis of Fmoc-Protected Amino Azides from Fmoc-Protected Amino Alcohols." Synlett, no. 2 (2006): 306–8. http://dx.doi.org/10.1055/s-2005-923589.

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30

Isidro-Llobet, Albert, Xavier Just-Baringo, Ariel Ewenson, Mercedes Álvarez, and Fernando Albericio. "Fmoc-2-mercaptobenzothiazole, for the introduction of the Fmoc moiety free of side-reactions." Biopolymers 88, no. 5 (2007): 733–37. http://dx.doi.org/10.1002/bip.20732.

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31

Kumar, Ashish, Anamika Sharma, Beatriz G. de la Torre та Fernando Albericio. "Scope and Limitations of γ-Valerolactone (GVL) as a Green Solvent to be Used with Base for Fmoc Removal in Solid Phase Peptide Synthesis". Molecules 24, № 21 (2019): 4004. http://dx.doi.org/10.3390/molecules24214004.

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GVL is a green solvent used in Fmoc-based solid-phase peptide synthesis. It is susceptible to ring opening in the presence of bases such as piperidines, which are used to remove the Fmoc protecting group. Here we studied the formation of the corresponding acyl piperidides by time-dependent monitoring using NMR. The results, corroborated by theoretical calculations, indicate that a solution of piperidines in GVL should be prepared daily for a better Fmoc removal.

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32

Mayans, Enric, and Carlos Alemán. "Revisiting the Self-Assembly of Highly Aromatic Phenylalanine Homopeptides." Molecules 25, no. 24 (2020): 6037. http://dx.doi.org/10.3390/molecules25246037.

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Diphenylalanine peptide (FF), which self-assembles into rigid tubular nanostructures, is a very short core recognition motif in Alzheimer’s disease β-amyloid (Aβ) polypeptide. Moreover, the ability of the phenylalanine (F or Phe)-homopeptides to self-assemble into ordered nanostructures has been proved. Within this context it was shown that the assembly preferences of this family of compounds is altered by capping both the N- and C-termini using highly aromatic fluorenyl groups (i.e., fluorenyl-9-methoxycarbonyl and 9-fluorenylmethyl ester, named Fmoc and OFm, respectively). In this article th

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33

Bojarska, Joanna, Milan Remko, Izabela D. Madura, Krzysztof Kaczmarek, Janusz Zabrocki, and Wojciech M. Wolf. "Synthesis, experimental and in silico studies of N-fluorenylmethoxycarbonyl-O-tert-butyl-N-methyltyrosine, coupled with CSD data: a survey of interactions in the crystal structures of Fmoc–amino acids." Acta Crystallographica Section C Structural Chemistry 76, no. 4 (2020): 328–45. http://dx.doi.org/10.1107/s2053229620003009.

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Recently, fluorenylmethoxycarbonyl (Fmoc) amino acids (e.g. Fmoc–tyrosine or Fmoc–phenylalanine) have attracted growing interest in biomedical research and industry, with special emphasis directed towards the design and development of novel effective hydrogelators, biomaterials or therapeutics. With this in mind, a systematic knowledge of the structural and supramolecular features in recognition of those properties is essential. This work is the first comprehensive summary of noncovalent interactions combined with a library of supramolecular synthon patterns in all crystal structures of amino

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34

Zanuy, David, Jordi Poater, Miquel Solà, Ian W. Hamley, and Carlos Alemán. "Fmoc–RGDS based fibrils: atomistic details of their hierarchical assembly." Physical Chemistry Chemical Physics 18, no. 2 (2016): 1265–78. http://dx.doi.org/10.1039/c5cp04269k.

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We describe the 3D supramolecular structure of Fmoc–RGDS fibrils, where Fmoc and RGDS refer to the hydrophobic N-(fluorenyl-9-methoxycarbonyl) group and the hydrophilic Arg-Gly-Asp-Ser peptide sequence, respectively.

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35

Murali, Dhanya Mahalakshmi, and Ganesh Shanmugam. "The aromaticity of the phenyl ring imparts thermal stability to a supramolecular hydrogel obtained from low molecular mass compound." New Journal of Chemistry 43, no. 31 (2019): 12396–409. http://dx.doi.org/10.1039/c9nj01781j.

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Using Fmoc-phenylalanine and Fmoc-cyclohexylalanine, we show that the aromaticity of the phenyl ring imparts significant thermal stability to a supramolecular hydrogel system and its significance depends on the method of inducing hydrogelation.

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36

Phillips, Ian R., and Elizabeth A. Shephard. "Endogenous Roles of Mammalian Flavin-Containing Monooxygenases." Catalysts 9, no. 12 (2019): 1001. http://dx.doi.org/10.3390/catal9121001.

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Flavin-containing monooxygenases (FMOs) catalyze the oxygenation of numerous foreign chemicals. This review considers the roles of FMOs in the metabolism of endogenous substrates and in physiological processes, and focuses on FMOs of human and mouse. Tyramine, phenethylamine, trimethylamine, cysteamine, methionine, lipoic acid and lipoamide have been identified as endogenous or dietary-derived substrates of FMOs in vitro. However, with the exception of trimethylamine, the role of FMOs in the metabolism of these compounds in vivo is unclear. The use, as experimental models, of knockout-mouse li

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37

Mehlmann, Heinz, Daniel Olschewski, Andrey Olschewski, and Martin Feigel. "Complexation of Organic Dyes by Peptides Built of Lysine and Glutamic Acid Amides." Zeitschrift für Naturforschung B 57, no. 3 (2002): 343–48. http://dx.doi.org/10.1515/znb-2002-0314.

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AbstractTwo amide libraries, Fmoc-[Lys(aci)]4-Gly-resin (1) (aci = 2-naphthylcarbonyl, 1-adamantylcarbonyl and benzyloxycarbonyl) and Fmoc-[δ-Glu(α-amidei)]4-Gly-resin (2) (amidei = morpholineamide, piperidineamide, (N´-phenyl)-piperazineamide), have been synthesized from the corresponding Fmoc-protected amino acid derivatives. Beads of the libraries complex organic dyes (crystal violet and Sudan black) differently according to the sequence of residues in 1 or 2. The results are considered a step towards artificial receptors for small organic molecules build from linear oligoamides.

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38

HENCZI, M., та D. F. WEAVER. "ChemInform Abstract: An Improved Synthesis of N.epsilon.-FMOC-L-lysine and Nδ-FMOC-L- ornithine." ChemInform 26, № 13 (2010): no. http://dx.doi.org/10.1002/chin.199513249.

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39

PERICH, JOHN W. "Efficient Fmoc/solid-phase synthesis of Abu(P)-containing peptides using Fmoc-Abu(PO3Me2)-OH." International Journal of Peptide and Protein Research 44, no. 3 (2009): 288–94. http://dx.doi.org/10.1111/j.1399-3011.1994.tb00172.x.

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40

Diaferia, Carlo, Giancarlo Morelli, and Antonella Accardo. "Fmoc-diphenylalanine as a suitable building block for the preparation of hybrid materials and their potential applications." Journal of Materials Chemistry B 7, no. 34 (2019): 5142–55. http://dx.doi.org/10.1039/c9tb01043b.

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Due to its capability to self-assemble in self-supporting hydrogels (HG) under physiological conditions, Fmoc-FF is one of the most studied ultra-short peptide. This feature pushed towards the development of novel Fmoc-FF multicomponent systems.

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41

Sebesta, Radovan, та Dieter Seebach. "Preparation of (S,S)-Fmoc-β2hIle-OH, (S)-Fmoc-β2hMet-OH, and (S)-Fmoc-β2hTyr(tBu)-OH for Solid-Phase Syntheses ofβ2- andβ2/β3-Peptides". Helvetica Chimica Acta 86, № 12 (2003): 4061–72. http://dx.doi.org/10.1002/hlca.200390337.

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42

Feagin, Trevor A., Nirmal I. Shah, and Jennifer M. Heemstra. "Convenient and Scalable Synthesis of Fmoc-Protected Peptide Nucleic Acid Backbone." Journal of Nucleic Acids 2012 (2012): 1–5. http://dx.doi.org/10.1155/2012/354549.

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The peptide nucleic acid backbone Fmoc-AEG-OBn has been synthesized via a scalable and cost-effective route. Ethylenediamine is mono-Boc protected, then alkylated with benzyl bromoacetate. The Boc group is removed and replaced with an Fmoc group. The synthesis was performed starting with 50 g of Boc anhydride to give 31 g of product in 32% overall yield. The Fmoc-protected PNA backbone is a key intermediate in the synthesis of nucleobase-modified PNA monomers. Thus, improved access to this molecule is anticipated to facilitate future investigations into the chemical properties and applications

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43

Shu, Lianhe, та Ping Wang. "Synthesis of Enantiopure Fmoc-α-Methylvaline". Organic Process Research & Development 12, № 2 (2008): 298–300. http://dx.doi.org/10.1021/op700286u.

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44

Zanna, Nicola, Andrea Merlettini, Giuseppina Tatulli, Lorenzo Milli, Maria Letizia Focarete, and Claudia Tomasini. "Hydrogelation Induced by Fmoc-Protected Peptidomimetics." Langmuir 31, no. 44 (2015): 12240–50. http://dx.doi.org/10.1021/acs.langmuir.5b02780.

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45

Fuentes, Edgar, Kamila Boháčová, Ana M. Fuentes‐Caparrós, et al. "PAINT‐ing Fluorenylmethoxycarbonyl (Fmoc)‐Diphenylalanine Hydrogels." Chemistry – A European Journal 26, no. 44 (2020): 9869–73. http://dx.doi.org/10.1002/chem.202001560.

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46

Lawrence, Stephen A. "N-(9-Fluorenylmethoxycarbonyl) Succinimide (Fmoc-ONSu)." ChemInform 34, no. 1 (2003): no. http://dx.doi.org/10.1002/chin.200301244.

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47

Draper, Emily R., Kyle L. Morris, Marc A. Little, et al. "Hydrogels formed from Fmoc amino acids." CrystEngComm 17, no. 42 (2015): 8047–57. http://dx.doi.org/10.1039/c5ce00801h.

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48

Nevalainen, Marta, Pasi M. Kauppinen, and Ari M. P. Koskinen. "Synthesis of Fmoc-Protectedtrans-4-Methylproline." Journal of Organic Chemistry 66, no. 6 (2001): 2061–66. http://dx.doi.org/10.1021/jo005726s.

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49

Meyer, Daniel, Roger Marti та Dieter Seebach. "Scalable Enantioselective Synthesis of Fmoc-β2-Serine and Fmoc-β2-Threonine by an Organocatalytic Mannich Reaction". European Journal of Organic Chemistry 2015, № 22 (2015): 4883–91. http://dx.doi.org/10.1002/ejoc.201500636.

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50

Browne, Elisse C., Steven J. Langford, and Belinda M. Abbott. "Peptide Nucleic Acid Monomers: A Convenient and Efficient Synthetic Approach to Fmoc/Boc Monomers." Australian Journal of Chemistry 65, no. 5 (2012): 539. http://dx.doi.org/10.1071/ch11471.

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A convenient and cost-effective method for the synthesis of Fmoc/Boc-protected peptide nucleic acid monomers is described. The Fmoc/Boc strategy was developed in order to eliminate the solubility issues during peptide nucleic acid solid-phase synthesis, in particular that of the cytosine monomer, that occurred when using the commercialized Bhoc chemistry approach.

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