4.8 Article

Catalytic Oligopeptide Synthesis

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ORGANIC LETTERS
卷 20, 期 3, 页码 612-615

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b03735

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资金

  1. KAKENHI from JSPS [25713002, 17H03025, JP16H01043]
  2. MEXT
  3. Shorai Foundation For Science and Technology
  4. Grants-in-Aid for Scientific Research [16K18856] Funding Source: KAKEN

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Waste-free catalytic assembly of alpha-amino acids is fueled by a multiboron catalyst that features a characteristic B3NO2 heterocycle, providing a versatile catalytic protocol wherein functionalized natural alpha-amino acid units are accommodated and commonly used protecting groups are tolerated. The facile dehydrative conditions eliminate the use of engineered peptide coupling reagents, exemplifying a greener catalytic alternative for peptide coupling. The catalysis is sufficiently robust to enable pentapeptide synthesis, constructing all four amide bond linkages in a catalytic fashion.

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