Copper-catalyzed substitution of allylic carbonates with diboron: A new approach to allylboronate synthesis

2008 ◽  
Vol 80 (5) ◽  
pp. 1039-1045 ◽  
Author(s):  
Hajime Ito ◽  
Shinichiro Ito ◽  
Yusuke Sasaki ◽  
Kou Matsuura ◽  
Masaya Sawamura

Copper-catalyzed γ-selective substitution of allylic carbonates with diboron provides a new method for the efficient synthesis of allylboronates. Optically active α-chiral allylboronates were synthesized through the reaction of chiral allylic carbonates with bis(pinacolato)diboron in the presence of achiral Cu(I)-catalyst with highly efficient chirality transfer. Additionally, in the presence of a chiral Cu(I) catalyst, optically active α-chiral allylboronates were obtained with >90 % ee through the reaction of prochiral substrates with the diboron.

1969 ◽  
Vol 47 (21) ◽  
pp. 4073-4076 ◽  
Author(s):  
K. G. Rutherford ◽  
J. L. H. Batiste ◽  
J. M. Prokipcak

A new method for the resolution of potentially optically active trityl alcohols is reported. Three trityl alcohols as pilot compounds were converted to hydracrylic acid derivatives. Esterification with diazo-methane was followed by degradation (reverse Michael reaction) to the original alcohols with sodium hydride. The resolution of phenyl-α-naphthyl-p-tolylcarbinol was effected conveniently by this route.


ChemInform ◽  
2003 ◽  
Vol 34 (5) ◽  
Author(s):  
Jose Villamizar ◽  
Angel L. Orcajo ◽  
Juan Fuentes ◽  
Eleonora Tropper ◽  
Randolph Alonso

2013 ◽  
Vol 31 (8) ◽  
pp. 992-996 ◽  
Author(s):  
Hengyu Qian ◽  
Shihai Yan ◽  
Xiuling Cui ◽  
Chao Pi ◽  
Cheng Liu ◽  
...  

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