Tandem one-pot synthesis of α-(aminomethylene)-γ-butyrolactones via regioselective epoxide ring-opening with the Blaise reaction intermediate

2010 ◽  
Vol 51 (52) ◽  
pp. 6893-6896 ◽  
Author(s):  
Young Ok Ko ◽  
Yu Sung Chun ◽  
Youngmee Kim ◽  
Sung Jin Kim ◽  
Hyunik Shin ◽  
...  
ChemInform ◽  
2011 ◽  
Vol 42 (13) ◽  
pp. no-no
Author(s):  
Young Ok Ko ◽  
Yu Sung Chun ◽  
Youngmee Kim ◽  
Sung Jin Kim ◽  
Hyunik Shin ◽  
...  

ChemInform ◽  
2015 ◽  
Vol 46 (9) ◽  
pp. no-no
Author(s):  
Azim Ziyaei Halimehjani ◽  
Seyyed Emad Hooshmand ◽  
Elham Vali Shamiri

ChemInform ◽  
2011 ◽  
Vol 42 (15) ◽  
pp. no-no
Author(s):  
Thirupathi Boningari ◽  
Andrea Olmos ◽  
Benjaram M. Reddy ◽  
Jean Sommer ◽  
Patrick Pale

2010 ◽  
Vol 2010 (33) ◽  
pp. 6338-6347 ◽  
Author(s):  
Thirupathi Boningari ◽  
Andrea Olmos ◽  
Benjaram M. Reddy ◽  
Jean Sommer ◽  
Patrick Pale

2014 ◽  
Vol 55 (40) ◽  
pp. 5454-5457 ◽  
Author(s):  
Azim Ziyaei Halimehjani ◽  
Seyyed Emad Hooshmand ◽  
Elham Vali Shamiri

Synthesis ◽  
2021 ◽  
Author(s):  
Marcus M. Sá ◽  
Adrielle P. Maximiano ◽  
Giovana S. Ramos ◽  
Marcelo V. Marques

AbstractA two-step procedure for the preparation of cyclopropanecarboxaldehyde-1,1-diester from a γ,δ-epoxyester and its synthetic versatility are described herein. The epoxide ring-opening/cyclopropanation process occurs in the presence of Mg(ClO4)2 under heating, resulting in cyclopropanemethanol-1,1-diester in 65% yield. A mild TEMPO-mediated oxidation of this substrate readily generated the corresponding aldehyde in 75% yield, which was applied in the one-pot synthesis of four cyclopropylidene-γ-lactams and three δ-lactams. In addition, vinylcyclopropanes were obtained through the Wittig reaction of the aldehyde with phosphonium salts and used as precursors for tetrahydrofurans.


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