Tetrahedron Letters p. 1713 - 1716 (1999)
Update date:2022-07-29
Topics:
Moro-Oka, Yoshihiro
Fukuda, Tsutomu
Iwao, Masatomo
The first total synthesis of veiutamine, a new type of pyrroroiminoquinone marine alkaloid bearing a p-hydroxybenzyl substituent at C-6, has been achieved. The key step of the synthesis is 6-selective functionalization of the 1,3,4,5-tetrahydropyrrolo[4,3,2-de]quinoline nucleus via N-Boc-directed lithiation.
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Doi:10.1021/ja9817141
(1999)Doi:10.1016/S0040-4039(99)00127-6
(1999)Doi:10.1021/ja9842114
(1999)Doi:10.1021/acs.orglett.0c00503
(2020)Doi:10.1021/jo991430e
(2000)Doi:10.1039/c5ra21801b
(2015)
