Abstract
The number of applications that use halogen bonding in the fields of self-assembly, supramolecular aggregation, and catalysis is growing. However, the accessibility of chiral halotriazoles shows that there is still a lot more to explore. The simple click-chemistry is applied for the straightforward synthesis of enantiomerically pure mono- and bidentate as well as multifunctional iodotriazole-based XB donors. The methodology is characterized by a wide variability due to easy access of chiral azides.
Original language | English |
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Pages (from-to) | 2128-2135 |
Number of pages | 8 |
Journal | Synthesis (Germany) |
Volume | 51 |
Issue number | 10 |
DOIs | |
Publication status | Published - 2019 |
MoE publication type | A1 Journal article-refereed |
Keywords
- chiral compounds
- click chemistry
- halogen bonds
- hydrogen bonds
- nitrogen heterocycles