Tetrahedron Letters p. 4815 - 4818 (1997)
Update date:2022-08-03
Topics:
Ito, Hisanaka
Sato, Azusa
Taguchi, Takeo
The development of a highly enantioselective aromatic Claisen rearrangement was achieved by the reaction of catechol motto allylic ethers with chiral boron reagent 1. This system was also shown to avoid the formation of para rearrangement and abnormal Claisen rearrangement products.
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Doi:10.1016/j.jorganchem.2010.08.054
(2011)Doi:10.1021/ja963261a
(1997)Doi:10.1016/S0040-4039(01)98896-3
(1968)Doi:10.1021/ja01846a048
(1941)Doi:10.1016/S0040-4039(97)01358-0
(1997)Doi:10.1021/om9704197
(1997)
