An upper-rim functionalized calix[4]arenebased thiourea installed onto the (R,R)-1,2-cyclohexanediamine scaffold was synthesized with a view to investigate its catalytic ability in enantioselective Michael additions.
Solvent-Free Enantioselective Michael Reactions Catalyzed by a Calixarene-Based Primary Amine Thiourea
	
	
	
		
		
		
		
		
	
	
	
	
	
	
	
	
		
		
		
		
		
			
			
			
		
		
		
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
		
		
		
	
DE SIMONE, NICOLA ALESSANDROMembro del Collaboration Group
;Sara Meninno
						
						
						
							Supervision
;Carmen Talotta
						
						
						
							Supervision
;Carmine GaetaMembro del Collaboration Group
;Placido Neri
						
						
						
							Writing – Original Draft Preparation
;Alessandra Lattanzi
						
						
						
							Writing – Original Draft Preparation
			2018
Abstract
An upper-rim functionalized calix[4]arenebased thiourea installed onto the (R,R)-1,2-cyclohexanediamine scaffold was synthesized with a view to investigate its catalytic ability in enantioselective Michael additions.File in questo prodotto:
	
	
	
    
	
	
	
	
	
	
	
	
		
			
				
			
		
		
	
	
	
	
		
		
			| File | Dimensione | Formato | |
|---|---|---|---|
| Solvent-Free Enantioselective Michael Reactions Catalyzed by a .pdf Open Access dal 01/06/2022 
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