ChemInform Abstract: Double Nucleophilic Addition to Acrolein with Ketene Silyl Acetals and Allylborolanes Catalyzed by Proline.

ChemInform ◽  
2011 ◽  
Vol 43 (2) ◽  
pp. no-no
Author(s):  
Makoto Shimizu ◽  
Mami Kawanishi ◽  
Akinori Itoh ◽  
Isao Mizota ◽  
Iwao Hachiya
2003 ◽  
Vol 44 (14) ◽  
pp. 2817-2821 ◽  
Author(s):  
Tomotaka Okino ◽  
Yasutaka Hoashi ◽  
Yoshiji Takemoto

ChemInform ◽  
2003 ◽  
Vol 34 (27) ◽  
Author(s):  
Tomotaka Okino ◽  
Yasutaka Hoashi ◽  
Yoshiji Takemoto

2012 ◽  
Vol 84 (12) ◽  
pp. 2609-2617 ◽  
Author(s):  
Takafumi Nishi ◽  
Isao Mizota ◽  
Makoto Shimizu

Recently, nucleophilic addition reactions to imino functions have been utilized in many crucial steps for the synthesis of bioactive and functional materials. This article summarizes the integrated “umpolung” reactions of α-imino esters and the use of iminium salts as reactive electrophiles. Regarding the umpolung reactions, the following five reactions are discussed: (1) N-alkylation/homocoupling; (2) tandem N-ethylation/C-allylation; (3) tandem N-ethylation/C-cyanation; (4) reduction of imines with tris(trimethylsilyl)aluminum; and (5) N-alkylation and Claisen rearrangement. Moreover, the generation and reactions of alkoxycarbonyl iminium species are also discussed. These are prepared easily from trisubstituted amino ketene silyl acetals by oxidation, and the subsequent nucleophilic addition of various nucleophiles readily affords the addition products.


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