ChemInform Abstract: SILYL ENOL ETHER FUNCTIONALIZATION. 3. REGIOSELECTIVE ACYLATION OF TRIMETHYLSILYL ENOL ETHERS WITH 2-ALKOXY-1,3-DIOXOLANES - SYNTHESIS OF α- AND Γ-PROTECTED DICARBONYL COMPOUNDS

1984 ◽  
Vol 15 (34) ◽  
Author(s):  
E. AKGUEN ◽  
U. PINDUR
1989 ◽  
Vol 54 (11) ◽  
pp. 2605-2608 ◽  
Author(s):  
V. V. Zhdankin ◽  
M. Mullikin ◽  
Rik Tykwinski ◽  
Bruce Berglund ◽  
Ronald Caple ◽  
...  

Author(s):  
Ha Rim Lee ◽  
Seo Yun Kim ◽  
Min Ji Park ◽  
Yong Sun Park

A novel synthetic strategy for highly enantioenriched cis-3,5-disubstituted γ-lactones has been developed by the AgOTf-promoted nucleophilic substitution of α-bromoacetates with silyl enol ethers and subsequent reductive lactonization. The utility of...


ChemInform ◽  
1989 ◽  
Vol 20 (47) ◽  
Author(s):  
V. V. ZHDANKIN ◽  
M. MULLIKIN ◽  
R. TYKWINSKI ◽  
B. BERGLUND ◽  
R. CAPLE ◽  
...  

RSC Advances ◽  
2020 ◽  
Vol 10 (46) ◽  
pp. 27874-27883
Author(s):  
Makoto Shimizu ◽  
Shingo Hata ◽  
Koichi Kondo ◽  
Kazuhiro Murakami ◽  
Isao Mizota ◽  
...  

While iminium salts generated from amino ketene silyl acetals react with silyl enol ethers, those from amino silyl enol ethers also undergo facile addition reactions to give alpha-amino ketone derivatives in good yields.


1983 ◽  
Vol 61 (7) ◽  
pp. 1379-1382 ◽  
Author(s):  
Roger N. Renaud ◽  
Denis Bérubé ◽  
Campbell J. Stephens

The formation of Mannich bases from the reaction of silyl enol ethers with N-methyl-N-mesitylmethyleniminium salt, generated by the electrochemical oxidation of N,N-dimethylmesidine, was studied. Important factors influencing the reaction are: (a) the silyl enol ether must be nucleophilic enough to react with the iminium salt and, at the same time, must be more difficult to oxidize than the tertiary amine, (b) the product of the reaction must not be oxidized at the operating potential. Examples are presented in this paper illustrating the successes and limitations of this reaction.


2022 ◽  
Author(s):  
Haoying Cao ◽  
Shanshan Ma ◽  
Yanhong Feng ◽  
Yawen Guo ◽  
Peng Jiao

Various β-nitro ketones, including those bearing a β-tertiary carbon, were prepared from geminal bromonitroalkanes and trimethylsilyl enol ethers of a broad range of ketones under visible light photoredox catalysis, which...


Author(s):  
Can Liu ◽  
Ni Shen ◽  
Rui Shang

Enamides and silyl enol ethers were alkylated to deliver products of N-acyl imines and ketones in the presence of a catalytic amount of N-tetrabutylammonium iodide under irradiation of purple light...


2011 ◽  
Vol 7 ◽  
pp. 648-652 ◽  
Author(s):  
Haruo Aikawa ◽  
Tetsuro Kaneko ◽  
Naoki Asao ◽  
Yoshinori Yamamoto

Unprecedented alkylation of silyl enol ethers has been developed by the use of ortho-alkynylbenzoic acid alkyl esters as alkylating agents in the presence of a gold catalyst. The reaction probably proceeds through the gold-induced in situ construction of leaving groups and subsequent nucleophilic attack on the silyl enol ethers. The generated leaving compound abstracts a proton to regenerate the silyl enol ether structure.


2013 ◽  
Vol 42 (7) ◽  
pp. 691-693 ◽  
Author(s):  
Mitsuru Kitamura ◽  
Kento Murakami ◽  
Yuichiro Shiratake ◽  
Tatsuo Okauchi
Keyword(s):  

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