National Changhua University of Education Institutional Repository : Item 987654321/14947
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 6458/11630
Visitors : 13914331      Online Users : 73
RC Version 3.2 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Adv. Search
LoginUploadHelpAboutAdminister

Please use this identifier to cite or link to this item: http://ir.ncue.edu.tw/ir/handle/987654321/14947

Title: Synthesis of Cyclo-2,2' :4',4'':2'',2''':4''',4'''':2'''',2'''':4''''',4-sexipyridine
Authors: Kelly, T. R.;Lee, Yean-Jang;Mears, R. J.
Contributors: 化學系
Date: 1997-05
Issue Date: 2012-12-10T02:51:25Z
Publisher: American Chemical Society
Abstract: Preparation of the title compound (2) by use of Stille couplings and a Kröhnke pyridine synthesis is described. By application of the Stille coupling reaction, preparation and functionalization of quater- and quinquepyridines 26, 27, and 28 were achieved. Elaboration of quinquepyridine 27 to the pyridinium salt 30 bearing a protected enal allowed for the synthesis of 2 by a one-pot deprotection/Kröhnke reaction in nine steps from 4,4‘-bipyridine. Use of the Kröhnke pyridine synthesis has been applied to prepare sexipyridine dibromide 19, but attempts to induce a macrocyclization via metal-mediated (Pd/Ni/Cu) aryl−aryl coupling procedures proved unsuccessful. Acetylene-bridged sexipyridines 3a and 3b incorporating 2,2‘-bipyridine units proved to be inaccessible via sp−sp2 or sp−sp coupling protocols.
Relation: J. Org. Chem., 62(9): 2774-2781
Appears in Collections:[Department of Chemistry] Periodical Articles

Files in This Item:

File SizeFormat
index.html0KbHTML299View/Open


All items in NCUEIR are protected by copyright, with all rights reserved.

 


DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback