871979-80-5Relevant articles and documents
Divergent total synthesis of the tricyclic marine alkaloids lepadiformine, fasicularin, and isomers of polycitorols by reagent-controlled diastereoselective reductive amination
In, Jinkyung,Lee, Seokwoo,Kwon, Yongseok,Kim, Sanghee
supporting information, p. 17433 - 17442 (2015/02/19)
We describe a flexible and divergent route to the pyrrolo-/pyrido[1,2-j]quinoline frameworks of tricyclic marine alkaloids via a common intermediate formed by the ester-enolate Claisen rearrangement of a cyclic amino acid allylic ester. We have synthesize
Formal total synthesis of (-)-lepadiformine
Lee, Minhee,Lee, Taeho,Kim, Eun-Young,Ko, Hyojin,Kim, Deukjoon,Kim, Sanghee
, p. 745 - 748 (2007/10/03)
A stereocontrolled approach to the preparation of the Weinreb intermediate 3 has been developed. The important features of this approach are the creation of stereogenic centers through a cyclic amino acid ester-enolate Claisen rearrangement and the use of