126266-12-4Relevant academic research and scientific papers
The organocatalytic enantioselective [3+2] cycloaddition reaction of α,β-unsaturated aldehydes with azomethine ylides applied to the asymmetric synthesis of densely substituted pyrroloisoquinolines
Iza, Ainara,Ugarriza, Iratxe,Uria, Uxue,Reyes, Efraím,Carrillo, Luisa,Vicario, Jose L.
, p. 8878 - 8884 (2013/09/23)
The synthesis of densely functionalized pyrrolo[2,1-a]isoquinolines was accomplished using the organocatalytic [3+2] cycloaddition between enals and azomethine ylides under iminium catalysis developed in our group some years ago as the key step. The cyclo
Two interrelated strategies for cephalotaxine synthesis
Lin, Xiaodong,Kavash, Robert W.,Mariano, Patrick S.
, p. 7335 - 7347 (2007/10/03)
Studies of two interrelated strategies for the synthesis of members of the cephalotaxus alkaloid family have culminated in a concise route for the preparation of the parent member cephalotaxine (1). As part of efforts exploring the use of an SET-promoted
