scholarly journals Lewis Acid Catalyzed Nucleophilic Substitutions of Propargylic and Allylic Silyl Ethers with Enol Silyl Ethers.

ChemInform ◽  
2003 ◽  
Vol 34 (21) ◽  
Author(s):  
Teruhiko Ishikawa ◽  
Toshiaki Aikawa ◽  
Yumiko Mori ◽  
Seiki Saito
Keyword(s):  
Lewis Acid ◽  
Nucleophilic Substitutions ◽  
Silyl Ethers ◽  
Acid Catalyzed ◽  
Enol Silyl Ethers

Lewis Acid-Catalyzed Nucleophilic Substitutions of Propargylic and Allylic Silyl Ethers with Enol Silyl Ethers

2003 ◽  
Vol 5 (1) ◽  
pp. 51-54 ◽  
Author(s):  
Teruhiko Ishikawa ◽  
Toshiaki Aikawa ◽  
Yumiko Mori ◽  
Seiki Saito
Keyword(s):  
Lewis Acid ◽  
Nucleophilic Substitutions ◽  
Silyl Ethers ◽  
Acid Catalyzed ◽  
Enol Silyl Ethers

Generation of a Lewis acid activated formaldimine and its reaction with enol silyl ethers. N-Unsubstituted aminomethylation

1992 ◽  
Vol 57 (26) ◽  
pp. 7009-7010 ◽  
Author(s):  
Keiji Tanino ◽  
Mitsumasa Takahashi ◽  
Koichi Murayama ◽  
Isao Kuwajima
Keyword(s):  
Lewis Acid ◽  
Silyl Ethers ◽  
Enol Silyl Ethers

ChemInform Abstract: Lewis Acid Promoted Nitroolefination of Enol Silyl Ethers via an Addition-Elimination Process.

ChemInform ◽  
2010 ◽  
Vol 30 (42) ◽  
pp. no-no
Author(s):  
Ji-Jun Chen ◽  
Takeo Kawabata ◽  
Hiroshi Ohnishi ◽  
Muhong Shang ◽  
Kaoru Fuji
Keyword(s):  
Lewis Acid ◽  
Elimination Process ◽  
Silyl Ethers ◽  
Enol Silyl Ethers

scholarly journals Electrogenerated Acid-Catalyzed Michael Reaction of Enol Silyl Ethers and Ketene Silyl Acetals to α,β-Unsaturated Carbonyl Compounds

1989 ◽  
Vol 62 (11) ◽  
pp. 3739-3741 ◽  
Author(s):  
Tsutomu Inokuchi ◽  
Yuji Kurokawa ◽  
Masahiko Kusumoto ◽  
Shinichi Tanigawa ◽  
Sadahito Takagishi ◽  
...  
Keyword(s):  
Carbonyl Compounds ◽  
Michael Reaction ◽  
Silyl Ethers ◽  
Acid Catalyzed ◽  
Silyl Acetals ◽  
Enol Silyl Ethers

scholarly journals Lewis Acid-Promoted Nitroolefination of Enol Silyl Ethers via an Addition Elimination Process.

1999 ◽  
Vol 47 (3) ◽  
pp. 394-397 ◽  
Author(s):  
Ji-Jun CHEN ◽  
Takeo KAWABATA ◽  
Hiroshi OHNISHI ◽  
Muhong SHANG ◽  
Kaoru FUJI
Keyword(s):  
Lewis Acid ◽  
Elimination Process ◽  
Silyl Ethers ◽  
Enol Silyl Ethers

Lewis acid catalyzed [2+2] cycloaddition of ynamides and propargyl silyl ethers: synthesis of alkylidenecyclobutenones and their reactivity in ring-opening and ring expansion

2016 ◽  
Vol 52 (61) ◽  
pp. 9574-9577 ◽  
Author(s):  
Ling Chen ◽  
Jian Cao ◽  
Zheng Xu ◽  
Zhan-Jiang Zheng ◽  
Yu-Ming Cui ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Ring Opening ◽  
Ring Expansion ◽  
Silyl Ethers ◽  
Acid Catalyzed

A family of four-membered enones, polysubstituted alkylidenecyclobutenones, were easily prepared by the Lewis acid catalyzed formal [2+2] cycloaddition of ynamides and propargyl silyl ethers.

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