References analysis of the Wikipedia article "Peptide synthesis" in the English version

doi.org

Isidro-Llobet A, Alvarez M, Albericio F (June 2009). "Amino acid-protecting groups". Chemical Reviews. 109 (6): 2455–2504. doi:10.1021/cr800323s. hdl:2445/69570. PMID 19364121. S2CID 90409290.

Jaradat DM (January 2018). "Thirteen decades of peptide synthesis: key developments in solid phase peptide synthesis and amide bond formation utilized in peptide ligation". Amino Acids. 50 (1): 39–68. doi:10.1007/s00726-017-2516-0. PMID 29185032. S2CID 3680612.

Merrifield RB (1963). "Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide". J. Am. Chem. Soc. 85 (14): 2149–2154. doi:10.1021/ja00897a025.

Mitchell AR (2008). "Bruce Merrifield and solid-phase peptide synthesis: a historical assessment". Biopolymers. 90 (3): 175–184. doi:10.1002/bip.20925. PMID 18213693. S2CID 30382016.

Mant CT, Chen Y, Yan Z, Popa TV, Kovacs JM, Mills JB, et al. (2007). "HPLC analysis and purification of peptides". Peptide Characterization and Application Protocols. Methods in Molecular Biology. Vol. 386. Humana Press. pp. 3–55. doi:10.1007/978-1-59745-430-8_1. ISBN 978-1-59745-430-8. PMC 7119934. PMID 18604941.

Tickler AK, Clippingdale AB, Wade JD (August 2004). "Amyloid-beta as a "difficult sequence" in solid phase peptide synthesis". Protein and Peptide Letters. 11 (4): 377–384. doi:10.2174/0929866043406986. PMID 15327371.

El-Faham A, Albericio F (November 2011). "Peptide coupling reagents, more than a letter soup". Chemical Reviews. 111 (11): 6557–6602. doi:10.1021/cr100048w. PMID 21866984.

Montalbetti CA, Falque V (2005). "Amide bond formation and peptide coupling". Tetrahedron. 61 (46): 10827–10852. doi:10.1016/j.tet.2005.08.031.

Valeur E, Bradley M (February 2009). "Amide bond formation: beyond the myth of coupling reagents". Chemical Society Reviews. 38 (2): 606–631. doi:10.1039/B701677H. PMID 19169468.

El-Faham A, Albericio F (November 2011). "Peptide coupling reagents, more than a letter soup". Chemical Reviews. 111 (11): 6557–6602. doi:10.1021/cr100048w. PMID 21866984.

Joullié MM, Lassen KM (2010). "Evolution of Amide Bond Formation". Arkivoc. viii (8): 189–250. doi:10.3998/ark.5550190.0011.816. hdl:2027/spo.5550190.0011.816.

Subirós-Funosas R, Prohens R, Barbas R, El-Faham A, Albericio F (September 2009). "Oxyma: an efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosion". Chemistry: A European Journal. 15 (37): 9394–9403. doi:10.1002/chem.200900614. PMID 19575348.

Carpino, Louis A.; Imazumi, Hideko; El-Faham, Ayman; Ferrer, Fernando J.; Zhang, Chongwu; Lee, Yunsub; Foxman, Bruce M.; Henklein, Peter; Hanay, Christiane; Mügge, Clemens; Wenschuh, Holger; Klose, Jana; Beyermann, Michael; Bienert, Michael (1 February 2002). "The Uronium/Guanidinium Peptide Coupling Reagents: Finally the True Uronium Salts". Angewandte Chemie International Edition. 41 (3): 441–445. doi:10.1002/1521-3773(20020201)41:3<441::AID-ANIE441>3.0.CO;2-N.

Mansour, Tarek; Bardhan, Sujata; Wan, Zhao-Kui (2010). "Phosphonium- and Benzotriazolyloxy-Mediated Bond-Forming Reactions and Their Synthetic Applications". Synlett (8): 1143–1169. doi:10.1055/s-0029-1219820. ISSN 0936-5214.

Albericio F, Bofill JM, El-Faham A, Kates SA (1998). "Use of Onium Salt-Based Coupling Reagents in Peptide Synthesis". J. Org. Chem. 63 (26): 9678–9683. doi:10.1021/jo980807y.

Albericio, Fernando; Cases, Marta; Alsina, Jordi; Triolo, Salvatore A.; Carpino, Louis A.; Kates, Steven A. (7 July 1997). "On the use of PyAOP, a phosphonium salt derived from HOAt, in solid-phase peptide synthesis". Tetrahedron Letters. 38 (27): 4853–4856. doi:10.1016/S0040-4039(97)01011-3. ISSN 0040-4039.

Hiebl, J.; Baumgartner, H.; Bernwieser, I.; Blanka, M.; Bodenteich, M.; Leitner, K.; Rio, A.; Rovenszky, F.; Alberts, D.P.; Bhatnagar, P.K.; Banyard, A.F.; Baresch, K.; Esch, P.M.; Kollmann, H.; Mayrhofer, G. (1999). "Large‐scale synthesis of hematoregulatory nonapeptide SK&F 107647 by fragment coupling". The Journal of Peptide Research. 54 (1): 54–65. doi:10.1034/j.1399-3011.1999.00089.x. ISSN 1397-002X.

Kent SB (1988). "Chemical synthesis of peptides and proteins". Annual Review of Biochemistry. 57 (1): 957–989. doi:10.1146/annurev.bi.57.070188.004521. PMID 3052294.

Feinberg RS, Merrifield RB (1974). "Zinc chloride-catalyzed chloromethylation of resins for solid phase peptide synthesis". Tetrahedron. 30 (17): 3209–3212. doi:10.1016/S0040-4020(01)97575-1.

Hermkens PH, Ottenheijm HC, Rees DC (1997). "Solid-phase organic reactions II: A review of the literature Nov 95 – Nov 96". Tetrahedron. 53 (16): 5643–5678. doi:10.1016/S0040-4020(97)00279-2.

Schnolzer MA, Jones A, Alewood D, Kent SB (2007). "In Situ Neutralization in Boc-chemistry Solid Phase Peptide Synthesis". Int. J. Peptide Res. Therap. 13 (1–2): 31–44. doi:10.1007/s10989-006-9059-7. S2CID 28922643.

Beyermann M, Bienert M (1992). "Synthesis of difficult peptide sequences: A comparison of Fmoc-and BOC-technique". Tetrahedron Letters. 33 (26): 3745–3748. doi:10.1016/0040-4039(92)80014-B.

Luna OF, Gomez J, Cárdenas C, Albericio F, Marshall SH, Guzmán F (November 2016). "Deprotection Reagents in Fmoc Solid Phase Peptide Synthesis: Moving Away from Piperidine?". Molecules. 21 (11): 1542. doi:10.3390/molecules21111542. PMC 6274427. PMID 27854291.

Huang H, Rabenstein DL (May 1999). "A cleavage cocktail for methionine-containing peptides". The Journal of Peptide Research. 53 (5): 548–553. doi:10.1034/j.1399-3011.1999.00059.x. PMID 10424350.

Dick F (1995). "Acid Cleavage/Deprotection in Fmoc/tBiu Solid-Phase Peptide Synthesis". In Pennington MW, Dunn BM (eds.). Peptide Synthesis Protocols. Methods in Molecular Biology. Vol. 35. Totowa, NJ: Humana Press. pp. 63–72. doi:10.1385/0-89603-273-6:63. ISBN 978-1-59259-522-8. PMID 7894609.

Katsoyannis PG, ed. (1973). The Chemistry of Polypeptides. New York: Plenum Press. doi:10.1007/978-1-4613-4571-8. ISBN 978-1-4613-4571-8. S2CID 35144893.

Bergmann M, Zervas L (1932). "Über ein allgemeines Verfahren der Peptid-Synthese". Berichte der deutschen chemischen Gesellschaft. 65 (7): 1192–1201. doi:10.1002/cber.19320650722.

Thieriet N, Alsina J, Giralt E, Guibé F, Albericio F (1997). "Use of Alloc-amino acids in solid-phase peptide synthesis. Tandem deprotection-coupling reactions using neutral conditions". Tetrahedron Letters. 38 (41): 7275–7278. doi:10.1016/S0040-4039(97)01690-0.

Shin DS, Kim DH, Chung WJ, Lee YS (September 2005). "Combinatorial solid phase peptide synthesis and bioassays". Journal of Biochemistry and Molecular Biology. 38 (5): 517–525. doi:10.5483/BMBRep.2005.38.5.517. PMID 16202229.

Price JV, Tangsombatvisit S, Xu G, Yu J, Levy D, Baechler EC, et al. (September 2012). "On silico peptide microarrays for high-resolution mapping of antibody epitopes and diverse protein-protein interactions". Nature Medicine. 18 (9): 1434–1440. doi:10.1038/nm.2913. PMC 3491111. PMID 22902875.

Hedberg-Dirk EL, Martinez UA (8 August 2010). "Large-Scale Protein Arrays Generated with Interferometric Lithography for Spatial Control of Cell-Material Interactions". Journal of Nanomaterials. 2010: e176750. doi:10.1155/2010/176750. ISSN 1687-4110.

Fodor SP, Read JL, Pirrung MC, Stryer L, Lu AT, Solas D (February 1991). "Light-directed, spatially addressable parallel chemical synthesis". Science. 251 (4995): 767–773. Bibcode:1991Sci...251..767F. doi:10.1126/science.1990438. PMID 1990438.

Tam JP, Wu CR, Liu W, Zhang JW (1991). "Disulfide bond formation in peptides by dimethyl sulfoxide. Scope and applications". J. Am. Chem. Soc. 113 (17): 6657–6662. doi:10.1021/ja00017a044.

Sieber P, Kamber B, Hartmann A, Jöhl A, Riniker B, Rittel W (January 1977). "[Total synthesis of human insulin. IV. Description of the final steps (author's transl)]". Helvetica Chimica Acta. 60 (1): 27–37. doi:10.1002/hlca.19770600105. PMID 838597.

Spears RJ, McMahon C, Chudasama V (October 2021). "Cysteine protecting groups: applications in peptide and protein science". Chemical Society Reviews. 50 (19): 11098–11155. doi:10.1039/D1CS00271F. PMID 34605832. S2CID 238258277.

Laps S, Atamleh F, Kamnesky G, Sun H, Brik A (February 2021). "General synthetic strategy for regioselective ultrafast formation of disulfide bonds in peptides and proteins". Nature Communications. 12 (1): 870. Bibcode:2021NatCo..12..870L. doi:10.1038/s41467-021-21209-0. PMC 7870662. PMID 33558523.

Ottl J, Battistuta R, Pieper M, Tschesche H, Bode W, Kühn K, Moroder L (November 1996). "Design and synthesis of heterotrimeric collagen peptides with a built-in cystine-knot. Models for collagen catabolism by matrix-metalloproteases". FEBS Letters. 398 (1): 31–36. doi:10.1016/S0014-5793(96)01212-4. PMID 8946948. S2CID 24688988.

Akaji K, Fujino K, Tatsumi T, Kiso Y (1993). "Total synthesis of human insulin by regioselective disulfide formation using the silyl chloride-sulfoxide method". Journal of the American Chemical Society. 115 (24): 11384–11392. doi:10.1021/ja00077a043.

Pedersen SL, Tofteng AP, Malik L, Jensen KJ (March 2012). "Microwave heating in solid-phase peptide synthesis". Chemical Society Reviews. 41 (5): 1826–1844. doi:10.1039/C1CS15214A. PMID 22012213.

Dryland A, Sheppard RC (1986). "Peptide synthesis. Part 8. A system for solid-phase synthesis under low pressure continuous flow conditions". Journal of the Chemical Society, Perkin Transactions 1: 125–137. doi:10.1039/p19860000125. ISSN 0300-922X.

Simon MD, Heider PL, Adamo A, Vinogradov AA, Mong SK, Li X, et al. (March 2014). "Rapid flow-based peptide synthesis". ChemBioChem. 15 (5): 713–720. doi:10.1002/cbic.201300796. PMC 4045704. PMID 24616230.

Spare LK, Laude V, Harman DG, Aldrich-Wright JR, Gordon CP (2018). "An optimised approach for continuous-flow solid-phase peptide synthesis utilising a rudimentary flow reactor". Reaction Chemistry & Engineering. 3 (6): 875–882. doi:10.1039/C8RE00190A. ISSN 2058-9883.

Gordon CP (January 2018). "The renascence of continuous-flow peptide synthesis - an abridged account of solid and solution-based approaches". Organic & Biomolecular Chemistry. 16 (2): 180–196. doi:10.1039/C7OB02759A. PMID 29255827.

Sletten ET, Nuño M, Guthrie D, Seeberger PH (December 2019). "Real-time monitoring of solid-phase peptide synthesis using a variable bed flow reactor". Chemical Communications. 55 (97): 14598–14601. doi:10.1039/C9CC08421E. hdl:21.11116/0000-0005-3E5F-D. PMID 31742308.

Muir TW, Sondhi D, Cole PA (June 1998). "Expressed protein ligation: a general method for protein engineering". Proceedings of the National Academy of Sciences of the United States of America. 95 (12): 6705–6710. Bibcode:1998PNAS...95.6705M. doi:10.1073/pnas.95.12.6705. PMC 22605. PMID 9618476.

Nilsson BL, Soellner MB, Raines RT (2005). "Chemical synthesis of proteins". Annual Review of Biophysics and Biomolecular Structure. 34: 91–118. doi:10.1146/annurev.biophys.34.040204.144700. PMC 2845543. PMID 15869385.

Kent SB (February 2009). "Total chemical synthesis of proteins". Chemical Society Reviews. 38 (2): 338–351. doi:10.1039/B700141J. PMID 19169452. S2CID 5432012.

Nyfeler R (7 November 1994). Peptide synthesis via fragment condensation. Methods in Molecular Biology. Vol. 35. New Jersey: Humana Press. pp. 303–316. doi:10.1385/0-89603-273-6:303. ISBN 978-0-89603-273-6. PMID 7894607.

Flood DT, Hintzen JC, Bird MJ, Cistrone PA, Chen JS, Dawson PE (September 2018). "Leveraging the Knorr Pyrazole Synthesis for the Facile Generation of Thioester Surrogates for use in Native Chemical Ligation". Angewandte Chemie International Edition in English. 57 (36): 11634–11639. doi:10.1002/anie.201805191. PMC 6126375. PMID 29908104.

"Peptide Thioesters for Native Chemical Ligation". Chemistry Views. 9 September 2018.
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handle.net

hdl.handle.net

Joullié MM, Lassen KM (2010). "Evolution of Amide Bond Formation". Arkivoc. viii (8): 189–250. doi:10.3998/ark.5550190.0011.816. hdl:2027/spo.5550190.0011.816.

nih.gov

pubmed.ncbi.nlm.nih.gov