dc.contributor.author | SENGE, MATHIAS | |
dc.date.accessioned | 2010-06-15T11:55:20Z | |
dc.date.available | 2010-06-15T11:55:20Z | |
dc.date.issued | 1994 | |
dc.date.submitted | 1994 | en |
dc.identifier.citation | H. Xie, D. A. Lee, M. O. Senge, K. M. Smith, Syntheses, Structure, Properties, and Chemistry of 1,1-Di(pyrrolyl)ethenes, Journal of the Chemical Society, Chemical Communications, 1994, 791 - 792 | en |
dc.identifier.other | Y | |
dc.description | PUBLISHED | en |
dc.description.abstract | Reaction of a 2-unsubstituted pyrrole with acetic anhydride and stannic chloride unexpectedly promotes
self-condensation to give symmetrical di( pyrroly1)ethene as a side-product in &lo% yield, but overall yields of
these 1,l-di(pyrro1yl)ethenes can be improved to 66% using a rational alternate route; structure and chemistry of
1 ,I-di(pyrroly1)ethenes 2 are discussed | en |
dc.description.sponsorship | This research was supported by grants from the National
Institutes of Health (HL 22252) and the Deutsche Forschungsgemeinschaft
(Se 5431 1-1). Mass spectrometric analyses were
performed by the UCSF Mass Spectrometry Facility (A. L.
Burlingame, Director) supported by the Biomedical Research
Technology Programme of the National Center for Research
Resources, NIH NCRR BRTP 01614. | en |
dc.format.extent | 791 | en |
dc.format.extent | 792 | en |
dc.language.iso | en | en |
dc.publisher | Royal Society of Chemistry | en |
dc.relation.ispartofseries | Journal of the Chemical Society, Chemical Communications; | |
dc.rights | Y | en |
dc.subject | Chemistry | en |
dc.title | Syntheses, Structure, Properties, and Chemistry of 1,1-Di(pyrrolyl)ethenes | en |
dc.type | Journal Article | en |
dc.type.supercollection | scholarly_publications | en |
dc.type.supercollection | refereed_publications | en |
dc.identifier.peoplefinderurl | http://people.tcd.ie/sengem | |
dc.identifier.rssinternalid | 29205 | |
dc.identifier.rssuri | http://dx.doi.org/10.1039/C39940000791 | en |
dc.identifier.uri | http://hdl.handle.net/2262/40141 | |