Recent updates on vinyl cyclopropanes, aziridines and oxiranes: access to heterocyclic scaffolds
Kiruthika Nachimuthu1, Jothi Lakshmi Nallasivam1
1Department of Chemistry, National Institute of Technology, Tiruchirappalli, Tiruchirappalli-620 015, Tamil Nadu, India. jothi@nitt.edu.
Abstract:
This present review delineates the repertoire of vinyl cyclopropanes and their stuctural analogues to accomplish a wide array of oxa-cycles, aza-cycles, and thia-cycles under transition metal catalysis and metal-free approaches from early 2019 to the present date. The generation of electrophilic π-allyl intermediates and 1-3/1-5-dipolarophile chemistry originating from VCPs are always green, step- and atom-economical and sustainable strategies in comparsion with prefunctionalized and/or C-H activation protocols. Here, the strained ring-system extends its applicability by relieving the strain to undergo a ring-expansion reaction to accomplish 5-9 membered carbo- and heterocyclic systems. The availability of chiral ligands in the ring-expansion reaction of VCPs and their analogues has paved the way to realizing asymmetric synthetic transformations.
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