| Literature DB >> 26713861 |
Marc Liniger1, David G VanderVelde1, Michael K Takase1, Mona Shahgholi1, Brian M Stoltz1.
Abstract
Derivatives of the fully twisted bicyclic amide <span class="Chemical">7-hypoquinuclidone are synthesized using a Schmidt-Aubé reaction. Their structures were unambiguously confirmed by X-ray diffraction analysis and extensive spectroscopic characterization. Furthermore, the stability and chemical reactivity of these anti-Bredt amides are investigated. 7-Hypoquinuclidonium tetrafluoroborate is shown to decompose to a unique nitrogen bound amide-BF3 complex of 7-hypoquinuclidone under anhydrous conditions and to react instantaneously with water making it one of the most reactive amides known to date.Entities:
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Year: 2016 PMID: 26713861 PMCID: PMC4878439 DOI: 10.1021/jacs.5b11750
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419