“…Brassinosteroids (BRs) are considered as a novel candidate of steroids that play a crucial role in antiviral activities in the recovery of patients suffering with herpetic and viral diseases [91]. Four analogues of 28-homocastasterone such as (22R,23R,24S)-3β-acetoxy-22, 23-dihydroxy-5α-stigmastan-6-one (1), (22R,23R,24S)-3β-bromo-22,23-dihydroxy-5α-stigmastan-6-one (2), (22R,23R,24S)-3β-acetoxy-5, 22, 23-trihydroxy-5α-stigmastan-6-one (3), and (22R,23R,24S) 3β-bromo-5,22,23-trihydroxy-5α-stigmastan-6-one [4] have been formed via an artificial pathway dependent upon regioselective ∆ 5 epoxidation and characterization was done from stigmasterol. Compounds 1 and 2 having a 5αH moiety were synthesized by a reductive opening of the 5β, 6β epoxy precursor, and compounds 3 and 4 having 5αOH moiety were attained through hydrolytic opening of a mixture of 5α, 6α and 5β, 6β epoxy precursors.…”