Microwave-assisted ring-closing metathesis of diallylamines: a rapid synthesis of pyrrole and pyrroline derivatives
Q Yang, XY Li, H Wu, WJ Xiao
Index: Yang, Qian; Li, Xin-Yong; Wu, Hong; Xiao, Wen-Jing Tetrahedron Letters, 2006 , vol. 47, # 23 p. 3893 - 3896
Full Text: HTML
Citation Number: 37
Abstract
The ring-closing metathesis (RCM) reactions of diallylamines occurred under controlled microwave irradiation. In addition to the high reaction rate, the key features of the reaction are that it can be carried out without deactivation of the substrates and without the use of Lewis acids.
Related Articles:
[Jafari; Mahmoudi; Mirjalili Journal of the Iranian Chemical Society, 2011 , vol. 8, # 3 p. 851 - 856]
C–N Bond Formation Catalysed by CuI Bonded to Polyaniline Nanofiber
[Arundhathi, Racha; Kumar, Desitti Chaitanya; Sreedhar, Bojja European Journal of Organic Chemistry, 2010 , # 19 p. 3621 - 3630]
[Reddy, V. Prakash; Kumar, A. Vijay; Rao, K. Rama Tetrahedron Letters, 2011 , vol. 52, # 7 p. 777 - 780]
[Amal Joseph; Priyadarshini; Lakshmi Kantam; Maheswaran Tetrahedron Letters, 2012 , vol. 53, # 12 p. 1511 - 1513]
[Kantam, M. Lakshmi; Ramani; Chakrapani Synthetic Communications, 2008 , vol. 38, # 4 p. 626 - 636]