SYNTHETIC STUDIES OF HALICHONDRIN-B, AN ANTITUMOR POLYETHER MACROLIDEISOLATED FROM A MARINE SPONGE .5. A HIGHLY CONCISE AND EFFICIENT SYNTHESIS OF THE C-37-APPROXIMATE-TO-C-54 TRICYCLIC JKL-RING PART
K. Horita et al., SYNTHETIC STUDIES OF HALICHONDRIN-B, AN ANTITUMOR POLYETHER MACROLIDEISOLATED FROM A MARINE SPONGE .5. A HIGHLY CONCISE AND EFFICIENT SYNTHESIS OF THE C-37-APPROXIMATE-TO-C-54 TRICYCLIC JKL-RING PART, Heterocycles, 42(1), 1996, pp. 99-104
A concise and efficient synthesis of C(37)similar to C-54 tricyclic JK
L-ring unit (2) of halichondrin B (1) utilizing C-2-symmetric spiroket
al derivative (5) as a synthetic key intermediate, easily provided fro
m dimethyl L-(+)-tartrate, is reported.