| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5281269 | Tetrahedron Letters | 2007 | 4 Pages | 
Abstract
												A two-step convenient sequence for the synthesis of previously inaccessible mono-Boc-protected bis-N-heterocyclic alkyl substituted ether derivatives 4 is described. Mitsunobu protocol was applied to the preparation of pyridinyl ether precursor 5. The reduction of the electron rich pyridinyl system 5 has been achieved catalytically using the combination of PtO2-H2SO4 or PtO2-pTsOH under a hydrogen atmosphere maintained by a gas balloon at ambient temperature.
Graphical abstractDownload full-size image
Keywords
												
											Related Topics
												
													Physical Sciences and Engineering
													Chemistry
													Organic Chemistry
												
											Authors
												Jianhua Chao, Mariam Israiel, Junying Zheng, Cynthia Aki, 
											