The Juliá-Colonna Type Asymmetric Epoxidation Reaction Catalyzed by Soluble Oligo-L-leucines Containing an α-Aminoisobutyric Acid Residue: Importance of Helical Structure of the Catalyst on Asymmetric Induction

2000 ◽  
Vol 29 (4) ◽  
pp. 366-367 ◽  
Author(s):  
Ryukichi Takagi ◽  
Akiko Shiraki ◽  
Toshiki Manabe ◽  
Satoshi Kojima ◽  
Katsuo Ohkata
1984 ◽  
Vol 62 (11) ◽  
pp. 2148-2154 ◽  
Author(s):  
B. D. Johnston ◽  
A. C. Oehlschlager

S-(−)- and R-(+)-frontalin (1,5-dimethyl-6,8-dioxabicyclo[3.2.1]octane) were prepared from (E)-2-methyl-2,6-heptadiene-1-ol utilizing the Sharpless asymmetric epoxidation reaction to induce chirality. The six-step synthetic sequence proceeded in approximately 50% overall yield and was found to be suitable for the preparation of multi-gram quantities of either enantiomer with ≥ 90% ee.


2016 ◽  
Vol 20 (06) ◽  
pp. 730-737 ◽  
Author(s):  
Pachiannan Sakthipriya ◽  
Nallamuthu Ananthi

Novel chiral porphyrin ligands were synthesized from four different chiral aldehydes. In situ transition metal complexes of these novel chiral porphyrin ligands were found to catalyze asymmetric epoxidation reaction of styrene possessing various substituents. The chiral epoxides were formed in excellent yield and ee.


2003 ◽  
Vol 7 (4) ◽  
pp. 509-513 ◽  
Author(s):  
Sylvia Baars ◽  
Karl-Heinz Drauz ◽  
Hans-Peter Krimmer ◽  
Stanley M. Roberts ◽  
Jörg Sander ◽  
...  

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