84391-90-2Relevant academic research and scientific papers
Alkyl transfer from C-C cleavage: Replacing the nitro group of nitro-olefins
Li, Guangxun,Wu, Lei,Lv, Gang,Liu, Hongxin,Fu, Qingquan,Zhang, Xiaomei,Tang, Zhuo
, p. 6246 - 6248 (2014)
Alkyl substituted Hantzsch esters are rationally used as alkylation reagents to replace the nitro groups of nitro olefins to give excellent yields of trans-olefins. The reaction mechanism is considered to proceed through a free radical mechanism, which is different from the corresponding transfer alkylation of imines. This journal is the Partner Organisations 2014.
A VERSATILE TOTAL SYNTHESIS OF XENOGNOSIN
Kamat,, Vinayak S.,Graden, David W.,Lynn, David G.,Steffens, John C.,Riopel, James L.
, p. 1541 - 1544 (2007/10/02)
Xenognosin, 4, the first identified host recognition substance for parasitic angiosperms has been synthesized by a route efficient for the preparation of several structural analoques.
