Coupling of Fmoc-amino acid chlorides mediated by activated commercial zinc
dust for the synthesis of peptides is described. The reaction is carried o
ut in an organic medium. The necessity of using an inorganic base like NaHC
O3/Na2CO3 or an organic base like DIEA/NMM/TEA/pyridine is circumvented. Th
e coupling is reasonably fast, clean, racemization free and high yielding.
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