107967-52-2Relevant academic research and scientific papers
Synthesis and Consecutive Double Diels-Alder Cycloadditions of 3-Methylene-5-phenylsulfinyl-1-pentene as a Synthetic Equivalent of Parent Cross-conjugated Triene, 3-Methylene-1,4-pentadiene
Wada, Eiji,Nagasaki, Noritaka,Kanemasa, Shuji,Tsuge, Otohiko
, p. 1491 - 1494 (2007/10/02)
3-Methylene-5-phenylsulfinyl-1-pentene undergoes stepwise double Diels-Alder cycloadditions with two different dienophiles to afford hydronaphthalene skeletons.This sequence corresponds to cross type of diene-transmissive Diels-Alder cycloaddition of pare
