Decarboxylative Mannich Reactions with Substituted Malonic Acid Half-Oxyesters

2021 ◽  
Vol 86 (8) ◽  
pp. 5452-5462
Author(s):  
Tania Xavier ◽  
Sylvie Condon ◽  
Christophe Pichon ◽  
Erwan Le Gall ◽  
Marc Presset
2016 ◽  
Vol 3 (2) ◽  
pp. 133-160 ◽  
Author(s):  
Ayndrila Ghosh ◽  
Sudipto Bhowmick ◽  
Anirban Mondal ◽  
Harekrishna Garai ◽  
Kartick C. Bhowmick

1981 ◽  
Vol 46 (8) ◽  
pp. 1800-1807 ◽  
Author(s):  
Zdeněk Vejdělek ◽  
Marie Bartošová ◽  
Miroslav Protiva

4-Chloromethyl-s-hydrindacene (VIIa) was transformed via the malonic acid derivatives VIIIa and IXa to the acid Xb which afforded in four steps the homological acid Xc. Reactions of chlorides of both acids (XIbc ) with dimethylamine, 1-methylpiperazine and 1-(2-hydroxyethyl)piperazine led to the amides XIIbc-XIVbc which were reduced with lithium aluminium hydride to the title compounds IVcd-VIcd. The amines obtained show central neuroleptic effects only in subtoxic doses; they are also potent local anaesthetics and have significant spasmolytic activity of the neurotropic as well as musculotropic type.


1987 ◽  
Vol 111 (3) ◽  
pp. 439-443 ◽  
Author(s):  
Stanislz.xlaw Idziak ◽  
Narcyz Piślewski

RSC Advances ◽  
2021 ◽  
Vol 11 (16) ◽  
pp. 9098-9111
Author(s):  
Salahudeen Shamna ◽  
C. M. A. Afsina ◽  
Rose Mary Philip ◽  
Gopinathan Anilkumar

Amino alkylation of an acidic α-proton of a carbonyl by formaldehyde and a primary/secondary amine or ammonia, affording a β-amino-carbonyl compound also known as a Mannich base is a valuable reaction. We focus on recent advances in Zn catalysed Mannich reactions.


Author(s):  
Ziyi Li ◽  
Nana Wang ◽  
Haibo Mei ◽  
Hiroyuki Konno ◽  
Vadim A. Soloshonok ◽  
...  

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