An article The Catalytic Regio- and Stereoselective Synthesis of 1,6-Diazabicyclo[4.3.0]nonane-2,7-diones WOS:000670661000006 published article about ASYMMETRIC 1,3-DIPOLAR CYCLOADDITIONS; MELDRUMS ACID; MULTICOMPONENT SYNTHESIS; AZOMETHINE IMINES; ANNULATION; CHEMISTRY; YLIDES in [Lebrene, Arthur; Martzel, Thomas; Gouriou, Laura; Levacher, Vincent; Oudeyer, Sylvain; Afonso, Carlos; Loutelier-Bourhis, Corinne; Briere, Jean-Francois] Normandie Univ, COBRA, CNRS, INSA Rouen,UNIROUEN, F-76000 Rouen, France; [Sanselme, Morgane] Univ Rouen, Normandie Univ, Lab SMS, EA3233, F-76821 Mont St Aignan, France in 2021, Cited 37. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5. Name: 4-Methoxybenzaldehyde
A straightforward synthesis of original 1,6-diazabicyclo[4.3.0]nonane-2,7-diones was achieved through a DBU-organocatalyzed multicomponent Knoevenagel-aza-Michael-Cyclocondensation reaction which takes advantage of an unprecedented highly regio- and diastereoselective conjugate addition of pyridazinones to alkylidene Meldrum’s acid intermediates. The key reactive intermediates of this complex process were analyzed by means of electrospray ionization mass spectrometry coupled to ion mobility spectrometry, allowing us to validate the proposed mechanism.
About 4-Methoxybenzaldehyde, If you have any questions, you can contact Lebrene, A; Martzel, T; Gouriou, L; Sanselme, M; Levacher, V; Oudeyer, S; Afonso, C; Loutelier-Bourhis, C; Briere, JF or concate me.. Name: 4-Methoxybenzaldehyde
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