B. Jyothirmai

TL;DR: In this paper, a ring opening with sodium azide in a [bmim]BF 4 /H 2 O or [bimim]PF 6 /H2 O (2:1) solvent system, under mild and neutral reaction conditions to afford the corresponding 2-azidoalcohols in high to quantitative yields.

TL;DR: In this article, a variety of N-tosylaziridines undergo ring opening with aromatic amines using a catalytic amount of lithium perchlorate in acetonitrile at ambient temperature to afford the corresponding 1,2-diamines in excellent yields.

TL;DR: Zinc metal mediated simple and efficient alkylation of cyclic secondary amines e.g., piperazines and morpholine with allyl bromide was described in this paper.

TL;DR: Aziridines react smoothly with potassium thiocyanate in the presence of a catalytic amount of lithium perchlorate in acetonitrile under mild reaction conditions to afford the corresponding β-aminothiocynates in high yields and with high regioselectivity as discussed by the authors.

TL;DR: Aziridines react smoothly with potassium thiocyanate in the presence of a catalytic amount of lithium perchlorate in acetonitrile under mild reaction conditions to afford the corresponding β-aminothiocynates in high yields and with high regioselectivity as mentioned in this paper.