Desymmetrisation of readily available symmetrical polyamines is an imp
ortant first step in the synthesis of many polyamine containing natura
l products. Likewise in the synthesis of polyamine amides which are po
tentially useful for gene delivery and as neuroprotectants, based upon
channel blocking toxins found in certain wasp and spider venoms. The
application of trifluoroacetyl as a protecting group allows unsymmetri
cal polyamine amides to be easily prepared on a gram scale. (C) 1997 E
lsevier Science Ltd. All rights reserved.