Nevertheless, with the key building block 8 in hand, we envisioned the synthesis of novel hymenialdisine analogues following standard Suzuki coupling protocols. [¹6] Treatment of 8 with 4-methoxyphenyl boronic acid (1.1 equiv) in the presence of Pd(PPh 3 ) 4 (1 mol%) and aqueous sodium carbonate (2 M) as base in a mixture of toluene and ethanol (1:1) at 70 ˚C for 12-16 h, gave the desired product along with minor amounts of the deprotected compound 9a (R = ...