Show simple item record

dc.contributor.authorLund, Kate-lyn A.R.
dc.contributor.authorThompson, Alison
dc.date.accessioned2018-11-14T18:30:36Z
dc.date.available2018-11-14T18:30:36Z
dc.date.issued2014
dc.identifier.citationLund, K. L. A., & Thompson, A. (2014). Synthesis of Symmetric meso-H-Dipyrrin Hydrobromides from 2-Formylpyrroles. Synlett, 25(08), 1142-1144. DOI: 10.1055/s-0033-1341066en_US
dc.identifier.urihttp://hdl.handle.net/10222/74956
dc.description- Post-print - Publisher copyright and source must be acknowledged - Link to Publisher version (www.thieme-connect.com) must be included if article has been published onlineen_US
dc.description.abstractThe reaction of 2-formyl pyrroles in acidic methanol gives the corresponding symmetric, meso-H 4,6-dipyrrin hydrobromides. This convenient strategy involves initial deformylation under the acidic conditions, followed by immediate in situ reaction of the resulting α-free pyrrole with the remaining 2-formyl pyrrole in solution to give the dipyrrin hydrobromide salt in good yield.en_US
dc.publisherSynletten_US
dc.titleSynthesis of symmetric meso-H dipyrrin hydrobromides from 2-formyl pyrrolesen_US
dc.typeArticleen_US
 Find Full text

Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record