Cyclopropanol derivatives as intermediates for organochemical synthesis
E Wenkert, RA Mueller, EJ Reardon Jr…
Index: Wenkert,E. et al. Journal of the American Chemical Society, 1970 , vol. 92, p. 7428 - 7436
Full Text: HTML
Citation Number: 77
Abstract
Abstract: A design of terpene synthesis based on the acid-induced transformations of cyclopropyl ethers and p-methoxycyclopropylcarbinols into quaternary a-methyl and a-vinyl carbonyl compounds, respectively, is described. Similar reactions with gem- dimethoxycyclopropanes are portrayed. A cyclopropylamine is shown to be inert. p- Methoxycyclopropanecarboxylic esters are converted into y-ketocarboxylic acid ...
Related Articles:
[Ono, Fumiaki; Inatomi, Yoshiko; Tada, Yuusuke; Mori, Masaki; Sato, Tsuneo Chemistry Letters, 2009 , vol. 38, # 1 p. 96 - 97]
IPy2BF4??Mediated Rearrangements of 1, 2??Difunctionalized Compounds and Olefins
[Fananas, Francisco J.; Alvarez-Perez, Monica; Rodriguez, Felix Chemistry - A European Journal, 2005 , vol. 11, # 20 p. 5938 - 5944]
IPy2BF4??Mediated Rearrangements of 1, 2??Difunctionalized Compounds and Olefins
[Fananas, Francisco J.; Alvarez-Perez, Monica; Rodriguez, Felix Chemistry - A European Journal, 2005 , vol. 11, # 20 p. 5938 - 5944]
[Khan, Shoeb R.; Bhanage, Bhalchandra M. Tetrahedron Letters, 2013 , vol. 54, # 45 p. 5998 - 6001]
Stereoselective hydrosilylation of enals and enones catalysed by palladium nanoparticles
[Benohoud, Meryem; Tuokko, Sakari; Pihko, Petri M. Chemistry - A European Journal, 2011 , vol. 17, # 30 p. 8404 - 8413]