Enantioselective Synthesis of 3,4-Dihydropyran Derivatives via Organocatalytic Michael Reaction of α,β-Unsaturated Enones

2012 ◽  
Vol 77 (8) ◽  
pp. 4136-4142 ◽  
Author(s):  
Yangbin Liu ◽  
Xiaohua Liu ◽  
Min Wang ◽  
Peng He ◽  
Lili Lin ◽  
...  
2006 ◽  
Vol 17 (6) ◽  
pp. 908-915 ◽  
Author(s):  
Henryk Krawczyk ◽  
Marcin Śliwiński ◽  
Jacek Kędzia ◽  
Jakub Wojciechowski ◽  
Wojciech M. Wolf

Tetrahedron ◽  
2010 ◽  
Vol 66 (51) ◽  
pp. 9708-9713 ◽  
Author(s):  
Hua-Meng Yang ◽  
Li Li ◽  
Ke-Zhi Jiang ◽  
Jian-Xiong Jiang ◽  
Guo-Qiao Lai ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 23 (40) ◽  
pp. no-no
Author(s):  
M. IHARA ◽  
A. HIRABAYASHI ◽  
N. TANIGUCHI ◽  
K. FUKUMOTO

Heterocycles ◽  
1989 ◽  
Vol 28 (1) ◽  
pp. 63 ◽  
Author(s):  
Keiichiro Fukumoto ◽  
Tetsuji Kametani ◽  
Masataka Ihara ◽  
Yoshinobu Takino

Tetrahedron ◽  
1994 ◽  
Vol 50 (8) ◽  
pp. 2583-2590 ◽  
Author(s):  
Achille Barco ◽  
Simonetta Benetti ◽  
Carmela De Risi ◽  
Gian P. Pollini ◽  
Romeo Romagnoli ◽  
...  

Author(s):  
Paul S. Riehl ◽  
Alistair D. Richardson ◽  
Tatsuhiro Sakamoto ◽  
Corinna Schindler

<div> <div> <p>An 8-step enantioselective synthesis of lingzhiol is described herein. The sense of an asymmetric Michael reaction is reversed by the choice of metal source, enabling facile access to both enantiomers. A spontaneous semipinacol ring contraction enables mild construction of the lingzhiol core, and radical-mediated benzylic oxidation proceeds in the presence of an unprotected secondary alcohol. This represents the shortest enantioselective synthesis of lingzhiol to date, and the only enantiodivergent approach to both enantiomers of this meroterpenoid natural product.</p> </div> </div>


2012 ◽  
Vol 77 (19) ◽  
pp. 8802-8808 ◽  
Author(s):  
Sumit K. Ray ◽  
Pradeep K. Singh ◽  
Nagaraju Molleti ◽  
Vinod K. Singh

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