1,1-Divinylallene
| dc.contributor.author | Cergol, Katie | |
| dc.contributor.author | Newton, Christopher | |
| dc.contributor.author | Lawrence, Andrew | |
| dc.contributor.author | Willis, Anthony | |
| dc.contributor.author | Paddon-Row, Michael | |
| dc.contributor.author | Sherburn, Michael | |
| dc.date.accessioned | 2015-12-10T22:56:46Z | |
| dc.date.issued | 2011 | |
| dc.date.updated | 2016-02-24T10:24:34Z | |
| dc.description.abstract | How to hit a triple: The title hydrocarbon, one of the most π-bond-rich small molecules, has been synthesized and characterized for the first time. This highly reactive hydrocarbon undergoes a new diene-transmissive, triple Diels-Alder cycloaddition sequ | |
| dc.identifier.issn | 1433-7851 | |
| dc.identifier.uri | http://hdl.handle.net/1885/60369 | |
| dc.publisher | Wiley-VCH Verlag GMBH | |
| dc.source | Angewandte Chemie International Edition | |
| dc.subject | Keywords: 1,1-divinylallene; C-C bonds; Diels-Alder cycloadditions; Diels-Alder reactions; One step; Ring systems; Small molecules; Olefins; Organic compounds; Synthesis (chemical); Cycloaddition 1,1-divinylallene; cycloaddition; Diels-Alder reactions; hydrocarbons | |
| dc.title | 1,1-Divinylallene | |
| dc.type | Journal article | |
| local.bibliographicCitation.issue | 44 | |
| local.bibliographicCitation.lastpage | 10428 | |
| local.bibliographicCitation.startpage | 10425 | |
| local.contributor.affiliation | Cergol, Katie, College of Physical and Mathematical Sciences, ANU | |
| local.contributor.affiliation | Newton, Christopher, College of Physical and Mathematical Sciences, ANU | |
| local.contributor.affiliation | Lawrence, Andrew, College of Physical and Mathematical Sciences, ANU | |
| local.contributor.affiliation | Willis, Anthony, College of Physical and Mathematical Sciences, ANU | |
| local.contributor.affiliation | Paddon-Row, Michael, University of New South Wales | |
| local.contributor.affiliation | Sherburn, Michael, College of Physical and Mathematical Sciences, ANU | |
| local.contributor.authoruid | Cergol, Katie, u4656221 | |
| local.contributor.authoruid | Newton, Christopher, u4802207 | |
| local.contributor.authoruid | Lawrence, Andrew, u4568554 | |
| local.contributor.authoruid | Willis, Anthony, u8512028 | |
| local.contributor.authoruid | Sherburn, Michael, u4053118 | |
| local.description.embargo | 2037-12-31 | |
| local.description.notes | Imported from ARIES | |
| local.identifier.absfor | 030503 - Organic Chemical Synthesis | |
| local.identifier.absseo | 970103 - Expanding Knowledge in the Chemical Sciences | |
| local.identifier.ariespublication | u4005981xPUB536 | |
| local.identifier.citationvolume | 50 | |
| local.identifier.doi | 10.1002/anie.201105541 | |
| local.identifier.scopusID | 2-s2.0-80055012811 | |
| local.identifier.thomsonID | 000297049300033 | |
| local.type.status | Published Version |
Downloads
Original bundle
1 - 1 of 1
Loading...
- Name:
- 01_Cergol_1,1-Divinylallene_2011.pdf
- Size:
- 581.23 KB
- Format:
- Adobe Portable Document Format