Author's Organization：The Institute of Physical and Chemical Research (RIKEN) The Institute of Physical and Chemical Research (RIKEN) The Institute of Physical and Chemical Research (RIKEN)
Published: March 15, 1996Received: January 16, 1996Available on J-STAGE: March 31, 2008Accepted: January 31, 1996
Advance online publication: -
Revised: -
The seven-membered S- and Y-ring systems of maitotoxin (1) were stereoselectively synthesized based on the rearrangement-ring expansion of the six-membered ethers having the mesylate group on the α-side chain.
