II For example, the reaction of 1.2-epoxyindan (I) with aziridine (111) afforded 1-aziridipyl-2-indanol (IV) which was readily converted to 1,4-bis(2-hy- droxy-1-indany1)piperazine (V). The latter also was prepared by the direct action of piperazine with 1.2-epoxyindan as deb 4 by Mousseron (6). The indanamines derived from 1,2- epoxyindan are listed in Table I. The nitrogen mustards (1711) were prepared by the chlorination of the corresponding alcohol (VI) Received ...