| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5227312 | Tetrahedron | 2008 | 7 Pages | 
Abstract
												An efficient and rapid synthesis of furo[3,2-b]pyridine 1 is described using a one-pot Sonogashira coupling/heteroannulation sequence. Regioselective lithiation of this synthon was performed leading to various 2-substituted furo[3,2-b]pyridines. Some of them were used as substrates for short functional synthesis of polyheterocycles.
Graphical abstractDownload full-size image
Related Topics
												
													Physical Sciences and Engineering
													Chemistry
													Organic Chemistry
												
											Authors
												Anthony Chartoire, Corinne Comoy, Yves Fort, 
											![First Page Preview: Furo[3,2-b]pyridine: a convenient unit for the synthesis of polyheterocycles Furo[3,2-b]pyridine: a convenient unit for the synthesis of polyheterocycles](/preview/png/5227312.png)