European Journal of Organic Chemistry p. 4662 - 4670 (2010)
Update date:2022-08-03
Topics:
Bhuiyan, M. Delower H.
Zhu, Kai-Xian
Jensen, Paul
Try, Andrew C.
The yields of ester-functionalised Troeger's base analogues are dramatically improved by incorporating an electron-donating group on the aromatic ring and/or enhancing solubil- ity of the aniline unit. In addition to 2,8-diester compounds, 1,7-, 3,9- and 4,10-diester-functionalised Troeger's base analogues have been prepared for the first time.
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