Abstract
The reactions of internal propargyl esters with B(C6F5)(3) provide access to stable zwitterionic 1,3-dioxolium compounds which are characterised by X-ray diffraction. These 6 pi-electron systems show no significant aromatic stabilisation.
- Title
- B(C6F5)(3) promoted cyclisation of internal propargyl esters: structural characterisation of 1,3-dioxolium compounds
- Creators - without role
- Max M. Hansmann - Heidelberg UniversityRebecca L. Melen - University of TorontoFrank Rominger - Heidelberg UniversityA. Stephen K. Hashmi - King Abdulaziz UniversityDouglas W. Stephan - King Abdulaziz University
- Publication Details
- Chemical communications (Cambridge, England), Vol.50(55), pp.7243-7245
- Publisher
- Royal Soc Chemistry
- Number of pages
- 3
- Grant note
- Fonds der Chemischen Industrie for a Chemiefonds scholarship; Fonds der Chemischen Industrie NSERC of Canada; Natural Sciences and Engineering Research Council of Canada (NSERC) award of a Canada Research Chair Studienstiftung des deutschen Volkes
- Identifiers
- 9936053708331
- Academic Unit
- King Abdulaziz University
- Language
- English
- Resource Type
- Journal article