Synthesis of Cyclic Derivatives of Carbonyl Compounds of Furan Series

2019 ◽  
Vol 89 (12) ◽  
pp. 2341-2344
Author(s):  
G. Z. Raskildina ◽  
Yu. G. Borisova ◽  
Sh. Sh. Dzhumaev ◽  
S. S. Zlotsky
1991 ◽  
Vol 27 (12) ◽  
pp. 1358-1364 ◽  
Author(s):  
M. Trushule ◽  
�. Kupche ◽  
I. Augustane ◽  
N. V. Verovskii ◽  
�. Lukevits ◽  
...  

Author(s):  
Yu. P. Kitaev ◽  
B. L. Moldaver ◽  
I. M. Skrebkova ◽  
V. G. Yakutovich

2018 ◽  
Vol 14 ◽  
pp. 3018-3024
Author(s):  
Rudolf Knorr ◽  
Barbara Schmidt

Sterically well-shielded against unsolicited Michael addition and polymerization reactions, α-metalated α-(1,1,3,3-tetramethylindan-2-ylidene)acetonitriles added reversibly to three small aldehydes and two bulky ketones at room temperature. Experimental conditions were determined for transfer of the nucleofugal title carbanion unit between different carbonyl compounds. These readily occurring retro-additions via C–C(O) bond fission may also be used to generate different metal derivatives of the nucleofugal anions as equilibrium components. Fluoride-catalyzed, metal-free desilylation admitted carbonyl addition but blocked the retro-addition.


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