ChemInform Abstract: Chiral Bidentate Lithium Amides Having a Chiral Amide Nitrogen for Enantioselective Deprotonation of 4-tert-Butylcyclohexanone.

ChemInform ◽  
2010 ◽  
Vol 29 (18) ◽  
pp. no-no
Author(s):  
H. CHATANI ◽  
M. NAKAJIMA ◽  
H. KAWASAKI ◽  
K. KOGA
Keyword(s):  
Amide Nitrogen ◽  
Lithium Amides ◽  
Enantioselective Deprotonation

Chiral Bidentate Lithium Amides Having a Chiral Amide Nitrogen for Enantioselective Deprotonation of 4-tert-Butylcyclohexanone

Heterocycles ◽  
1997 ◽  
Vol 46 (1) ◽  
pp. 53 ◽  
Author(s):  
Kenji Koga ◽  
Haruko Chatani ◽  
Makoto Nakajima ◽  
Hisashi Kawasaki
Keyword(s):  
Amide Nitrogen ◽  
Lithium Amides ◽  
Enantioselective Deprotonation

ChemInform Abstract: Stereochemistry of Enantioselective Deprotonation of 4-Substituted Cyclohexanones by Chiral Bidentate Lithium Amides.

ChemInform ◽  
2010 ◽  
Vol 28 (17) ◽  
pp. no-no
Author(s):  
M. TORIYAMA ◽  
K. SUGASAWA ◽  
M. SHINDO ◽  
N. TOKUTAKE ◽  
K. KOGA
Keyword(s):  
Lithium Amides ◽  
Enantioselective Deprotonation

1,3-Dioxan-5-ones: synthesis, deprotonation, and reactions of their lithium enolates

1995 ◽  
Vol 73 (10) ◽  
pp. 1616-1626 ◽  
Author(s):  
Marek Majewski ◽  
D. Mark Gleave ◽  
Pawel Nowak
Keyword(s):  
Enantiomeric Excess ◽  
Addition Reactions ◽  
Synthetic Route ◽  
Enol Ethers ◽  
Lithium Amide ◽  
Silyl Enol Ethers ◽  
Lithium Amides ◽  
Alkyl Groups ◽  
Lithium Enolates ◽  
Enantioselective Deprotonation

A general synthetic route to 2-alkyl- and 2,2-dialkyl-1,3-dioxan-5-ones, using tris(hydroxymethyl)-nitromethane as the starting material, is described. Deprotonation of these compounds was studied. It was established that these dioxanones could be deprotonated with LDA; however, the reduction of the carbonyl group via a hydride transfer from LDA, giving the corresponding dioxanols, often competed with deprotonation. The reduction could be minimized by using Corey's internal quench procedure to form silyl enol ethers and was less pronounced in 2,2-dialkyldioxanones (ketals) than in 2-alkyldioxanones (acetals). Self-aldol products were observed when dioxanone lithium enolates were quenched with H2O. Addition reactions of lithium enolates of dioxanones to aldehydes were threo-selective as predicted by the Zimmerman–Traxler model. Dioxanones having two different alkyl groups at the 2-position were deprotonated enantioselectively by chiral lithium amide bases with enantiomeric excess (ee) of up to 70%. Keywords: 1,3-dioxan-5-ones, enantioselective deprotonation, chiral lithium amides.

Sign in / Sign up

Export Citation Format

Share Document