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DOI: 10.1055/s-0041-1738549
1H-Fluoren-9-ylmethyl Chloroformate as a Coupling Reagent for Peptide Synthesis
Significance
The development of a rapid, racemization-free, practically simple, and cost-effective methods for the synthesis of peptides is an important process in peptide drug discovery. In 2003, Sureshbabu and co-workers developed 1H-fluoren-9-ylmethyl chloroformate (Fmoc-Cl) as an effective coupling reagent for the synthesis of peptides.
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Comment
N-Protected amino acids smoothly reacted with a series of amino acid esters to provide various peptides in good yields with the help of Fmoc-Cl as a coupling reagent. This method is practically simple, rapid, and racemization-free; moreover, Fmoc-Cl is a commercially available, crystalline, bench-stable solid.
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Publication History
Article published online:
18 August 2022
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