Tetrahedron Letters p. 2427 - 2430 (1997)
Update date:2022-08-03
Topics:
Ghosh, Arun K.
Mathivanan, Packiarajan
Cappiello, John
The C3-C14 segment of the novel antitumor agent laulimalide has been constructed enantioselectively by utilizing a catalytic asymmetric hetero Diels-Alder reaction of benzyloxyacetaldehyde and Danishefsky's diene followed by Ferrier rearrangement and asymmetric conjugate reaction as the key steps.
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Doi:10.1021/jm00309a003
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(2020)Doi:10.1016/S0022-1139(01)00372-4
(2001)Doi:10.1021/ja01550a047
(1958)Doi:10.1016/S0040-4020(01)92573-6
(1967)Doi:10.1139/v97-037
(1997)
