SYNTHESIS OF HOMOLOGATED HALOVINYL DERIVATIVES FROM ARISTEROMYCIN ANDTHEIR INHIBITION OF HUMAN PLACENTAL S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE

Moffatt oxidation of 2',3'-O-isopropylidenearisteromycin (la) and trea tment of the 5'-carboxaldehyde with [(p-tolylsulfonyl)methylene] triph enylphosphorane gave the homologated vinylsulfone 2. Treatment of 2 wi th tributylstannane/AIBN gave the (E/Z)-vinylstannanes which were conv erted into the E and Z fluoro-and iodovinyl analogs. Chain extension v ia the 5'-cyano-5'-deoxy derivative 10a gave the 6'-carboxaldehyde of homoaristeromycin. S-Adenosyl-L-homocysteine hydrolase was strongly in hibited by the fluorovinyl, 5b, and iodovinyl, 4b and 7b, compounds, a nd time-dependent kinetics were observed [1-2 mu M (K-i) and 0.1-0.2 m in(-1) (k(inact))]. The mechanism of inactivation was shown to involve addition of water at the vinyl 5' or 6' carbons with elimination of h alide.