Tetrahedron Letters p. 535 - 538 (1992)
Update date:2022-08-04
Topics:
O'Sullivan, Patrick J.
Moreno, Rafael
Murphy, William S.
The new bromoquinone-enamine annulation was successfully extended to acyclic enamino ketones resulting in a new synthesis of the ABC framework 7 of kinamycins and when applied to cyclic enamino ketones 8a-c the first synthesis of their ABCD ring system.Smooth aromatisation of compounds 4b,d to 9a,b respectively was effected with DDQ. - Key Words: regiospecific annulation, metal catalysed; kinamycin; tetrahydrobenzocarbazole
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Doi:10.1126/science.aao0270
(2017)Doi:10.1016/j.ejmech.2012.07.013
(2012)Doi:10.1039/c8nj04867c
(2018)Doi:10.1021/acs.orglett.0c03529
(2020)Doi:10.1246/bcsj.65.66
(1992)Doi:10.1016/0022-328X(92)83137-7
(1992)
