scholarly journals Condensation Reactions of Aminoalcohols with Imides. I. Condensation Products of N, N-Diethylaminoethanol with Various Imides; Formation of N, N-Diethylenediamine

1960 ◽  
Vol 81 (2) ◽  
pp. 323-327 ◽  
Author(s):  
Kazuo NAKAJIMA
2020 ◽  
Vol 17 (1) ◽  
pp. 47-66
Author(s):  
Franz Bracher

Dimethylformamide acetals and Bredereck’s reagent (tert-butoxy-bis(dimethylamino) methane) are versatile C1 building blocks due to their ability to undergo condensation reactions with CH-acidic methyl and methylene moieties. Subsequent modulation of the resulting condensation products enables the preparation of open-chain products like aldehydes, ketones, enones, enol ethers, methyl groups, and, most important in alkaloid total synthesis, the annulation of heterocyclic rings like pyridines, pyridine-N-oxides, bromopyridines, aminopyridines, aminopyrimidines, pyrroles and chromenones. In certain cases, these reagents can act as alkylating agents. The applications of these building blocks in natural products total synthesis are reviewed here.


2018 ◽  
Vol 47 (48) ◽  
pp. 17469-17478 ◽  
Author(s):  
Laura Abad Galán ◽  
Alexandre N. Sobolev ◽  
Eli Zysman-Colman ◽  
Mark I. Ogden ◽  
Massimiliano Massi

Structures varying from polynuclear assemblies to coordination polymers are formed when β-triketonate ligands undergo retro-Claisen condensation reactions in the presence of lanthanoids.


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