Pd-Catalyzed Three-Component Reaction of 3-(Pinacolatoboryl)ally Acetates, Aldehydes, and Organoboranes: A New Entry to Stereoselective Synthesis of (Z)-anti-Homoallylic Alcohols

2015 ◽  
Vol 17 (11) ◽  
pp. 2824-2827 ◽  
Author(s):  
Yoshikazu Horino ◽  
Ataru Aimono ◽  
Hitoshi Abe
2017 ◽  
Vol 19 (21) ◽  
pp. 5968-5971 ◽  
Author(s):  
Yoshikazu Horino ◽  
Miki Sugata ◽  
Itaru Mutsuura ◽  
Keisuke Tomohara ◽  
Hitoshi Abe

2021 ◽  
Vol 08 ◽  
Author(s):  
Chithaluri Sudhakar ◽  
Pochamoni Ramudu

: An efficient stereoselective synthesis of 2,6-disubstituted-4-thiocyanatotetrahydropyrans has been developed through a one pot three-component reaction of aldehydes, trimethyl allylsilane and NH4SCN in the presence of BF3.Et2O at room temperature. The products are formed rapidly (10-30 min) in excellent yields (78-98%).


ChemInform ◽  
2003 ◽  
Vol 34 (1) ◽  
pp. no-no
Author(s):  
Marco Lombardo ◽  
Stefano Morganti ◽  
Massimo Tozzi ◽  
Claudio Trombini

2019 ◽  
Vol 55 (75) ◽  
pp. 11199-11202 ◽  
Author(s):  
Shang Gao ◽  
Ming Chen

A Cu-catalyzed stereoselective carboboration of dienylboronate for the synthesis of (E)-γ′,δ-bisboryl-anti-homoallylic alcohols was developed.


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