Synthesis of symmetric diester-functionalised Tröger's base analogues

M. Delower H Bhuiyan; Kai Xian Zhu; Paul Jensen; Andrew C. Try

doi:10.1002/ejoc.201000086

Synthesis of symmetric diester-functionalised Tröger's base analogues

M. Delower H Bhuiyan, Kai Xian Zhu, Paul Jensen, Andrew C. Try

Department of Molecular Sciences

Research output: Contribution to journal › Article

11 Citations (Scopus)

Abstract

The yields of ester-functionalised Tröger'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 Tröger's base analogues have been prepared for the first time.

Original language	English
Pages (from-to)	4662-4670
Number of pages	9
Journal	European Journal of Organic Chemistry
Issue number	24
DOIs	https://doi.org/10.1002/ejoc.201000086
Publication status	Published - Aug 2010

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abstract = "The yields of ester-functionalised Tr{\"o}ger'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 Tr{\"o}ger's base analogues have been prepared for the first time.",

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