A versatile synthesis of oligocrown compounds with hydroxyl groups at the hinge
- 1 January 1987
- journal article
- Published by Institute of Organic Chemistry & Biochemistry in Collection of Czechoslovak Chemical Communications
- Vol. 52 (12) , 2961-2970
- https://doi.org/10.1135/cccc19872961
Abstract
Oxirane ring-opening reaction of N-(2,3-epoxy-1-propyl) azacrowns Ia-Ic and 4,5-epoxy-2-oxapentylcrowns IIa-IIe with mono- and diamines (including mono- and diazacrowns) afforded array of new di-, tri-, and tetracrown compounds with hydroxyl groups placed at the hinge.Keywords
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