SUBSTITUTED TRI-PEPTIDE DERIVATIVES SYNTHESIS, CHARACTERIZATION
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Abrar Alzaydi, Rahul Islam Barbhuiya, Winny Routray, Abdallah Elsayed, Ashutosh Singh. Bioactive peptides: Synthesis, applications, and associated challenges. Food Bioengineering 2023, 12 https://doi.org/10.1002/fbe2.12057
Hisashi Masui, Shinichiro Fuse. Recent Advances in the Solid- and Solution-Phase Synthesis of Peptides and Proteins Using Microflow Technology. Organic Process Research & Development 2022, 26 (6) , 1751-1765. https://doi.org/10.1021/acs.oprd.2c00074
Yuma Otake, Kyohei Adachi, Yoshiaki Yamashita, Natsumi Iwanaga, Hirokatsu Sunakawa, Taiki Shamoto, Jun-ichi Ogawa, Atsushi Ito, Yutaka Kobayashi, Keiichi Masuya, Shinichiro Fuse, Daisuke Kubo, Hidenosuke Itoh. A liquid-phase continuous-flow peptide synthesizer for preparing C-terminal free peptides. Reaction Chemistry & Engineering 2023, 20 https://doi.org/10.1039/D2RE00453D
Kaminski, Z.J.; Paneth, P.; Rudzinski, J.A. Study on the activation of carboxylic acids by means of 2-chloro-4,6-dimethoxy-1,3,5-triazine and 2-chloro-4,6-diphenoxy-1.3.5-triazine. J. Org. Chem. 1998, 63, 4248–4225.
Hisashi Masui, Shinichiro Fuse. Recent Advances in the Solid- and Solution-Phase Synthesis of Peptides and Proteins Using Microflow Technology. Organic Process Research & Development 2022, 26 (6) , 1751-1765. https://doi.org/10.1021/acs.oprd.2c00074
Ayman El‐Faham, Fernando Albericio. Carpino's protecting groups, beyond the Boc and the Fmoc. Peptide Science 2020, 112 (4) https://doi.org/10.1002/pep2.24164
Yeon Sun Lee. Gram‐Scale Preparation of C‐Terminal‐Modified Enkephalin Analogues by Typical Liquid‐Phase Peptide Synthesis. Current Protocols in Protein Science 2019, 98 (1) https://doi.org/10.1002/cpps.97
Manashjyoti Konwar, Nageshwar D Khupse, Prakash J Saikia, Diganta Sarma. A potential greener protocol for peptide coupling reactions using recyclable/reusable ionic liquid [ $$hbox {C}_{4}hbox {-DABCO}][hbox {N(CN)}_{2}$$ C 4 -DABCO ] [ N(CN) 2 ]. Journal of Chemical Sciences 2018, 130 (5) https://doi.org/10.1007/s12039-018-1461-0
Decoene K.W., Vannecke W., Passioura T., Suga H., Madder A. PyrroleMediated Peptide Cyclization Identified through Genetically Reprogrammed Peptide Synthesis. Biomedicines. 2018;6:99
Caspar A, Reichert J. Future directions for peptide therapeutics development. Drug DiscovToday 2013;18:807–817.
Atherton E, Sheppard RC. The fluorenylmethoxycarbonyl amino protecting group. In: Udenfriend S, Meienhofer J, editors. The Peptides. Academic Press; New York: 1987. Pp. 1–38.
R.B. Merrifield, Automated synthesis of peptides; Science, 150 (1965), pp. 178-185, 10.1126/science.150.3693.178
Adam Přibylka, Viktor Krchňák, Eva Schütznerová. Environmentally Friendly SPPS II: Scope of Green Fmoc Removal Protocol Using NaOH and Its Application for Synthesis of Commercial Drug Triptorelin. The Journal of Organic Chemistry 2020, 85 (14) , 8798-8811.
Subirós-Funosas R, Prohens R, Barbas R, El-Faham A, Albericio F. Oxyma: an efficient additive for peptide synthesis to replace benzotriazole-based HOBt and HOAt with a lower risk of explosion. ChemEur J 2009;15:9394 – 9403.
B S. Patil, G R Vasanthakumar, V Suresh babu; Microwave assisted wolff rearrangement: A facile method for the synthesis of Fmoc –β-amino acids Letters in peptide science, 9; 2002, 231-233.
N S Sudarshan & V Suresh babu; Microwave accelerated high speed solution synthesis of peptides employing HATU/HOAt; Indian j.of chem, 44B, 2005, 1509-1511.
James ESheppeck, HeidiKar, HuiHong; A convenient and scaleable procedure For removing the Fmoc group in solution; Tetrahedron Letters; 2000; 41[28]; 5329-5333
Nishita Singh, Roohi Kesherwani, Arun Kumar Tiwari and Dilip Kumar Patel; A review on diabetes mellitus; The Pharma Innovation Journal 2016; 5(7): 36-40
Henninot, A.; Collins, J. C.; Nuss, J. M. The Current State of Peptide Drug Discovery: Back to the Future?. J. Med. Chem. 2018, 61, 1382, DOI: 10.1021/acs.jmedchem.7b00318
Hojo, K.; Ichikawa, H.; Onishi, M.; Fukumori, Y.; Kawasaki, K. Peptide synthesis “in water” by a solution-phase method using water-dispersible nanoparticle Boc-amino acids. J. Pept. Sci. 2011, 17, 487–492.
DOI: https://doi.org/10.37591/rrjodfdp.v10i1.1309
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