Abstract A convenient and modular synthesis involving diastereoselective Michael addition followed by regioselective Huisgen 1, 3-dipolar cycloaddition reaction was carried out to furnish 1, 4-disubstituted-1, 2, 3-triazoles of Ludartin. This reaction scheme involving Michael addition followed by regioselective Huisgen 1, 3-dipolar cycloaddition reaction leading to the formation of triazolyl analogs is being reported for the first time. All the ...