I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
It is employed in the design, synthesis, and evaluation of a family of propargyl pyridinyl ethers as potential cytochrome p450 inhibitors.
K. Tsuda, et al. Notes - Reaction Between Acrolein and Ethyl β-Aminocrotonate.J. Org. Chem.,1956,21(7), 800-801.
Roel J. E. M. De Weerd, et al. A new class of chiral detergents. The formation of single micelles from N,N-dimethyl-1-dodecyl-2,4-dimethyl-3-carbamoylpyridinium bromide. A CD study.J. Org. Chem.,1984,49(18), 3413-3415.