916982-61-1Relevant academic research and scientific papers
From acyclic to cyclic α-amino vinylphosphonates by using ring-closing metathesis
Adler, Pauline,Fadel, Antoine,Prunet, Jo?lle,Rabasso, Nicolas
supporting information, p. 387 - 395 (2017/01/13)
Acyclic α-amino vinylphosphonates were alkylated through the Mitsunobu reaction then diolefinic compounds hence formed were subjected to RCM. Studies on the scope and limitations of RCM with these sterically hindered α-amino vinylphosphonates are detailed
Gold-catalyzed cycloisomerizations of ene-ynamides
Couty, Sylvain,Meyer, Christophe,Cossy, Janine
body text, p. 1809 - 1832 (2009/06/28)
The gold-catalyzed cycloisomerizations of 1,6-ene-ynamides proceed under mild conditions and lead to cyclobutanones from terminal or trimethylsilyl substituted ynamides, or to carbonyl compounds bearing a 2,3-methanopyrrolidine subunit from substrates pos
