Synlett p. 713 - 715 (1997)
Update date:2022-08-03
Topics:
Tsuboi, Katsunori
Ichikawa, Yoshiyasu
Isobe, Minoru
One of the three spiro-segments in the synthesis of okadaic acid was synthesized under a new heteroconjugate addition strategy. Successive coupling of this spiro-segment with two tautomycin-synthetic segments afforded a hybrid molecule between okadaic acid and tautomycin.
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Doi:10.1002/chem.200305297
(2004)Doi:10.1021/om970408d
(1997)Doi:10.1016/j.bmcl.2006.07.014
(2006)Doi:10.1016/S0040-4020(97)00354-2
(1997)Doi:10.1021/ol016175a
(2001)Doi:10.1007/BF02495423
(1997)
