Stereocontrolled ring-opening of some enantiomerically enriched epoxy ketones and epoxy alcohols using trimethylaluminium: synthesis of (S )-2-arylpropanoic acids

2000 ◽  
pp. 2455-2463 ◽  
Author(s):  
Lydia Carde ◽  
D. Huw Davies ◽  
Stanley M. Roberts
Keyword(s):  
Ring Opening ◽  
Epoxy Ketones ◽  
Epoxy Alcohols

ChemInform Abstract: NEIGHBORING GROUP EFFECTS IN EPOXIDE RING OPENING, CIS-EPOXY-ALCOHOLS

1976 ◽  
Vol 7 (42) ◽  
pp. no-no
Author(s):  
ERWIN GLOTTER ◽  
PNINA KRINSKY ◽  
MIRIAM REJTOE ◽  
MARTIN WEISSENBERG
Keyword(s):  
Ring Opening ◽  
Epoxide Ring ◽  
Neighboring Group ◽  
Epoxide Ring Opening ◽  
Epoxy Alcohols ◽  
Group Effects

Boronic acid-catalysed C-3 selective ring opening of 3,4-epoxy alcohols with thiophenols and thiols

2019 ◽  
Vol 17 (7) ◽  
pp. 1901-1905 ◽  
Author(s):  
Hongqing Yao ◽  
Jiawei Liu ◽  
Chuan Wang
Keyword(s):  
Boronic Acid ◽  
Ring Opening ◽  
Selective Ring Opening ◽  
Epoxy Alcohols

A boronic acid-catalysed C-3 selective ring opening of 3,4-epoxy alcohols with thiophenols and thiols as nucleophiles has been accomplished.

Base- and Co(II)-Catalyzed Ring-Opening Reactions of Perhydrooxireno[2,3-d][1,2]dioxines:  An Efficient Route to 4-Hydroxy-2,3-epoxy-ketones

2003 ◽  
Vol 68 (13) ◽  
pp. 5205-5210 ◽  
Author(s):  
Ben W. Greatrex ◽  
Natalie F. Jenkins ◽  
Dennis K. Taylor ◽  
Edward R. T. Tiekink
Keyword(s):  
Ring Opening ◽  
Ring Opening Reactions ◽  
Efficient Route ◽  
Epoxy Ketones
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