From Lewis acids to peptide chemistry

Keywords

Peptides / protection free / non-racemization

References

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[2] Yamamoto H.“Designer acids”: combined acid catalysis for asymmetric synthesis.Angew Chem Int Ed Engl2005;44:1924-42

[3] Bhadra S.Substrate directed asymmetric reactions.Chem Rev2018;118:3391-446

[4] Sawano T.Substrate-directed catalytic selective chemical reactions.J Org Chem2018;83:4889-904

[5] Isidro-Llobet A,Mukherjee S.Sustainability challenges in peptide synthesis and purification: from R&D to production.J Org Chem2019;84:4615-28

[6] Tsuji H.Hydroxy-directed amidation of carboxylic acid esters using a tantalum alkoxide catalyst.J Am Chem Soc2016;138:14218-21

[7] Muramatsu W,Yamamoto H.Substrate-directed lewis-acid catalysis for peptide synthesis.J Am Chem Soc2019;141:12288-95

[8] Muramatsu W.Peptide bond formation of amino acids by transient masking with silylating reagents.J Am Chem Soc2021;143:6792-7

[9] Hattori T.Synthesis of silacyclic dipeptides: peptide elongation at both N- and C-termini of dipeptide.J Am Chem Soc2022;144:1758-65

[10] Yamamoto H. Unpublished