Synfacts 2022; 18(09): 1051
DOI: 10.1055/s-0041-1738549
Peptide Chemistry

1H-Fluoren-9-ylmethyl Chloroformate as a Coupling Reagent for Peptide Synthesis

Contributor(s):
Hisashi Yamamoto
,
Isai Ramakrishna
Tantry SJ, Vasanthakumar G.-R, Sureshbabu VV. * Bangalore University, India
Synthesis of Peptides Employing 9-Fluorenylmethyl Chloroformate as a Coupling Agent.

Lett. Pept. Sci. 2003;
10: 51-55
DOI: 10.1023/B:LIPS.0000014009.88440.14.
 

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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