Titelbild: Enantioselective Construction of Quaternary Stereogenic Centers from Tertiary Boronic Esters: Methodology and Applications (Angew. Chem. 16/2011)

2011 ◽  
Vol 123 (16) ◽  
pp. 3655-3655
Author(s):  
Ravindra P. Sonawane ◽  
Vishal Jheengut ◽  
Constantinos Rabalakos ◽  
Robin Larouche-Gauthier ◽  
Helen K. Scott ◽  
...  
2011 ◽  
Vol 123 (16) ◽  
pp. 3844-3847 ◽  
Author(s):  
Ravindra P. Sonawane ◽  
Vishal Jheengut ◽  
Constantinos Rabalakos ◽  
Robin Larouche-Gauthier ◽  
Helen K. Scott ◽  
...  

ChemInform ◽  
2011 ◽  
Vol 42 (34) ◽  
pp. no-no
Author(s):  
Ravindra P. Sonawane ◽  
Vishal Jheengut ◽  
Constantinos Rabalakos ◽  
Robin Larouche-Gauthier ◽  
Helen K. Scott ◽  
...  

2011 ◽  
Vol 50 (16) ◽  
pp. 3760-3763 ◽  
Author(s):  
Ravindra P. Sonawane ◽  
Vishal Jheengut ◽  
Constantinos Rabalakos ◽  
Robin Larouche-Gauthier ◽  
Helen K. Scott ◽  
...  

2011 ◽  
Vol 50 (16) ◽  
pp. 3575-3575 ◽  
Author(s):  
Ravindra P. Sonawane ◽  
Vishal Jheengut ◽  
Constantinos Rabalakos ◽  
Robin Larouche-Gauthier ◽  
Helen K. Scott ◽  
...  

2014 ◽  
Vol 136 (7) ◽  
pp. 2682-2694 ◽  
Author(s):  
Ilan Marek ◽  
Yury Minko ◽  
Morgane Pasco ◽  
Tom Mejuch ◽  
Noga Gilboa ◽  
...  

Synthesis ◽  
2019 ◽  
Vol 51 (15) ◽  
pp. 2959-2964 ◽  
Author(s):  
Yoshiyasu Ichikawa ◽  
Hirofumi Morimoto ◽  
Toshiya Masuda

A new approach was developed to construct quaternary stereogenic centers bearing nitrogen substituents in an enantioselective manner. The strategy takes advantage of [1,3]-chirality transfer from a chiral primary alcohol equivalent through an allyl cyanate-to-isocyanate rearrangement. This approach was employed in an efficient eight-step synthesis of the marine natural product, (+)-geranyllinaloisocyanide, in 43% overall yield.


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