| Literature DB >> 19548691 |
John T Henssler1, Adam J Matzger.
Abstract
An optimized synthetic methodology which allows for efficient and scalable access to the important fused-ring heterocycle thieno[3,2-b]thiophene and the first reported isolation of thieno[3,2-b]furan is presented. The properties of thieno[3,2-b]furan were assessed through a detailed analysis of the NMR data and an investigation of the chemical reactivity. Thieno[3,2-b]furan is chemically robust and offers good selectivity toward functionalization at the 2-position via bromination and the 5-position via deprotonation.Entities:
Year: 2009 PMID: 19548691 DOI: 10.1021/ol9010745
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005