TY - JOUR
T1 - Two-Component Redox Organocatalyst for Peptide Bond Formation
AU - Handoko,
AU - Panigrahi, Nihar R.
AU - Arora, Paramjit S.
N1 - Funding Information:
The authors would like to thank the National Science Foundation for financial support of this work (CHE- 2108150). The authors would also like to thank Alexander Radosevich (MIT) for a generous gift of 1,2,2,3,4,4-hexamethylphosphetane oxide.
Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/3/2
Y1 - 2022/3/2
N2 - Peptides are fundamental therapeutic modalities whose sequence-specific synthesis can be automated. Yet, modern peptide synthesis remains atom uneconomical and requires an excess of coupling agents and protected amino acids for efficient amide bond formation. We recently described the rational design of an organocatalyst that can operate on Fmoc amino acids─the standard monomers in automated peptide synthesis (J. Am. Chem. Soc. 2019, 141, 15977). The catalytic cycle centered on the conversion of the carboxylic acid to selenoester, which was activated by a hydrogen bonding scaffold for amine coupling. The selenoester was generated in situ from a diselenide catalyst and stoichiometric amounts of phosphine. Although the prior system catalyzed oligopeptide synthesis on solid phase, it had two significant requirements that limited its utility as an alternative to coupling agents─it depended on stoichiometric amounts of phosphine and required molecular sieves as dehydrating agent. Here, we address these limitations with an optimized method that requires only catalytic amounts of phosphine and no dehydrating agent. The new method utilizes a two-component organoreductant/organooxidant-recycling strategy to catalyze amide bond formation.
AB - Peptides are fundamental therapeutic modalities whose sequence-specific synthesis can be automated. Yet, modern peptide synthesis remains atom uneconomical and requires an excess of coupling agents and protected amino acids for efficient amide bond formation. We recently described the rational design of an organocatalyst that can operate on Fmoc amino acids─the standard monomers in automated peptide synthesis (J. Am. Chem. Soc. 2019, 141, 15977). The catalytic cycle centered on the conversion of the carboxylic acid to selenoester, which was activated by a hydrogen bonding scaffold for amine coupling. The selenoester was generated in situ from a diselenide catalyst and stoichiometric amounts of phosphine. Although the prior system catalyzed oligopeptide synthesis on solid phase, it had two significant requirements that limited its utility as an alternative to coupling agents─it depended on stoichiometric amounts of phosphine and required molecular sieves as dehydrating agent. Here, we address these limitations with an optimized method that requires only catalytic amounts of phosphine and no dehydrating agent. The new method utilizes a two-component organoreductant/organooxidant-recycling strategy to catalyze amide bond formation.
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U2 - 10.1021/jacs.1c12798
DO - 10.1021/jacs.1c12798
M3 - Article
C2 - 35188383
AN - SCOPUS:85125554062
SN - 0002-7863
VL - 144
SP - 3637
EP - 3643
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 8
ER -