Synthetic electrochemistry for peptides

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2. Electrifying organic synthesis10.1002/anie.201711060 ↗

3. Modern electrochemical aspects for the synthesis of value-added organic products10.1002/anie.201712732 ↗

4. Electrochemical strategies for C−H functionalization and C−N bond formation10.1039/C7CS00619E ↗

5. Organic electrochemistry: molecular syntheses with potential10.1021/acscentsci.0c01532 ↗

6. Liquid-phase peptide synthesis (LPPS): a third wave for the preparation of peptides10.1021/acs.chemrev.2c00132 ↗

7. Advances in solid-phase peptide synthesis in aqueous media (ASPPS)10.1039/D2GC02319A ↗

8. Sustainability in peptide chemistry: current synthesis and purification technologies and future challenges10.1039/D1GC04387K ↗

9. Greening Fmoc/tBu solid-phase peptide synthesis10.1039/C9GC03982A ↗

10. Sustainability challenges in peptide synthesis and purification: from R&D to production10.1021/acs.joc.8b03001 ↗

11. Electrochemistry for the chemoselective modification of peptides and proteins10.1021/jacs.1c11185 ↗

12. Electrochemical late-stage functionalization10.1021/acs.chemrev.3c00158 ↗

13. Electrochemical-induced cross-coupling for organic and bioorganic synthesis

14. Electrogenerated cationic reactive intermediates: the pool method and further advances10.1021/acs.chemrev.7b00475 ↗

15. Modern strategies in electroorganic synthesis10.1021/cr0680843 ↗

16. Redox catalysis in organic electrosynthesis: basic principles and recent developments10.1039/c3cs60464k ↗

17. Tunable electrochemical peptide modifications: unlocking new levels of orthogonality for side-chain functionalization10.1002/anie.202215470 ↗

18. Fine-tuning electroauxiliary-mediated peptide modifications using second-generation electroactive amino acids10.1021/acs.orglett.3c00988 ↗

19. On the use of triarylsilanols as catalysts for direct amidation of carboxylic acids10.1021/acs.joc.3c00585 ↗

20. Heterocyclic boron acid catalyzed dehydrative amidation of aliphatic/aromatic carboxylic acids with amines10.1021/acs.joc.2c02515 ↗

21. Less is more: N(BOH)2 configuration exhibits higher reactivity than the B3NO2 heterocycle in catalytic dehydrative amide formation10.1021/acs.orglett.2c04382 ↗

22. Organocatalytic activation of inert hydrosilane for peptide bond formation10.1021/acs.orglett.2c02947 ↗

23. Diboronic acid anhydride-catalyzed direct peptide bond formation enabled by hydroxy-directed dehydrative condensation10.1021/acs.orglett.0c03252 ↗

24. Catalytic dehydrative peptide synthesis with gem-diboronic acids10.1021/acscatal.9b03894 ↗

25. A novel protecting group for constructing combinatorial peptide libraries10.1246/bcsj.74.733 ↗

26. A practical solution-phase synthesis of an antagonistic peptide of TNF-α based on hydrophobic tag strategy10.1039/c0cc03090b ↗

27. Tag-assisted liquid-phase peptide synthesis using hydrophobic benzyl alcohols as supports10.1021/jo302127d ↗

28. Acid-triggered colorimetric hydrophobic benzyl alcohols for soluble tag-assisted liquid-phase synthesis10.1021/acs.orglett.5b02057 ↗

29. Photo-triggered fluorometric hydrophobic benzyl alcohol for soluble tag-assisted liquid-phase peptide synthesis10.1002/ajoc.201700401 ↗

30. AJIPHASE®: a highly efficient synthetic method for one-pot peptide elongation in the solution phase by an Fmoc strategy10.1002/anie.201702931 ↗

31. Silylated tag-assisted peptide synthesis: continuous one-pot elongation for the production of difficult peptides under environmentally friendly conditions10.3390/molecules26123497 ↗

32. Silicon-based hydrophobic tags applied in liquid-phase peptide synthesis: protected DRGN-1 and poly alanine chain synthesis10.1039/D2OB01795D ↗

33. (Non-)Kolbe electrolysis in biomass valorization – a discussion of potential applications10.1039/C9GC03264A ↗

34. Advances in electrochemical decarboxylative transformation reactions10.1002/chem.202001764 ↗

35. Electrosynthesis using carboxylic acid derivatives: new tricks for old reactions10.1021/acs.accounts.9b00586 ↗

36. Electrochemical oxidation induced selective C–C bond cleavage10.1021/acs.chemrev.0c00335 ↗

37. Total synthesis of biseokeaniamides A−C and late-stage electrochemically-enabled peptide analogue synthesis10.1039/D0SC03701J ↗

38. An electrochemical approach to designer peptide α-amides inspired by α-amidating monooxygenase enzymes10.1021/jacs.1c05718 ↗

39. Electrochemistry of phosphorus and sulfur compounds: a unique tool for organic synthesis10.1021/ar970329y ↗

40. Comparative study of the N-isobutyl-(2E,6Z)-dodecadienamide chemical and electrochemical syntheses10.1039/B815745F ↗

41. [We note that it is debatable to consider triphenylphosphine as a true mediator in electrochemical reactions. Normally, a mediator is activated electrochemically and returns to its inactive state after conversion of the substrate. It is then electrochemically re-generated, either in situ (in-cell mediation) or in a separate step (ex-cell mediation). Here, the term mediator simply means that the method is indirect].

42. Biphasic electrochemical peptide synthesis10.1039/D1SC03023J ↗

43. Site-selective photocatalytic functionalization of peptides and proteins at selenocysteine10.1038/s41467-022-34530-z ↗

44. An umpolung approach for the chemoselective arylation of selenocysteine in unprotected peptides10.1021/jacs.5b05447 ↗

45. A chemoselective strategy for late-stage functionalization of complex small molecules with polypeptides and proteins10.1038/s41557-018-0154-0 ↗

46. Chemoselective copper-mediated modification of selenocysteines in peptides and proteins10.1021/jacs.1c06101 ↗

47. Assessment of reagents for selenocysteine conjugation and the stability of selenocysteine adducts10.1039/C6OB00775A ↗

48. Utilizing selenocysteine for expressed protein ligation and bioconjugations10.1021/jacs.6b10991 ↗

49. Stable and potent selenomab-drug conjugates10.1016/j.chembiol.2017.02.012 ↗

50. Electrochemical modification of polypeptides at selenocysteine10.1002/anie.202313037 ↗