Soaking Up Synthesis

Soaking Up Synthesis

Author: David Bradley

One of the most fascinating manzamine natural products is nakadomarin A, which was isolated by Kobayashi in 1997 from an Okinawan sponge Amphimedon sp. It has a complex 6/5/5/5/8/15 hexacyclic ring system and embodies a furan ring.

Kobayashi suggested a biosynthetic route to the structure, but now a concise synthesis that includes an enecarbamate Michael addition/furan-N-acyliminium ion cascade cyclization leads to the tetracyclic core. Mark Nilson and Raymond Funk, Pennsylvania State University, USA, then employed a ring-closing alkyne and alkene metatheses which allowed them to construct the fifteen- and eight-membered azacycles, respectively.


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