A New Method for Oxidation of Various Alcohols to the Corresponding Carbonyl Compounds by UsingN-t-Butylbenzenesulfinimidoyl Chloride

2002 ◽  
Vol 75 (2) ◽  
pp. 223-234 ◽  
Author(s):  
Jun-ichi Matsuo ◽  
Daisuke Iida ◽  
Kazuya Tatani ◽  
Teruaki Mukaiyama
2019 ◽  
Author(s):  
Zhen Liu ◽  
Xiaohan Li ◽  
Tian Zeng ◽  
Keary Engle

A substrate-directed enantioselective <i>anti</i>-carboboration reaction of alkenes has been developed, wherein a carbon based nucleophile and a boron moiety are installed across the C=C bond through a 5- or 6-membered palladacycle intermediate. The reaction is promoted by a palladium(II) catalyst and a mondentate oxzazoline ligand. A range of enantioenriched secondary alkylboronate products were obtained with moderate to high enantioselectivity that could be further upgraded by recrystallization. This work represents a new method to synthesize versatile and valuable alkylboronate building blocks. Building on an earlier mechanistic proposal by Peng, He, and Chen, a revised model is proposed to account for the stereoconvergent nature of this transformation.


1984 ◽  
Vol 15 (47) ◽  
Author(s):  
T. IMAMOTO ◽  
T. TAKEYAMA ◽  
M. YOKOYAMA

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