1353455-69-2

Downstream Products

• 1353455-87-4 (Z)-N-(2-oxabicyclo[3.2.0]heptan-7-ylidenemethyl)-N-(4-fluorobenzyl)-4-methylbenzenesulfonamide 
• 1353455-83-0 (Z)-N-(2-oxabicyclo[4.2.0]octan-8-ylidenemethyl)-N-(4-fluorobenzyl)-4-methylbenzenesulfonamide 
• 1353456-26-4 (Z)-N-(4-fluorobenzyl)-N-((2-(N-(4-fluorobenzyl)-4-methylphenylsulfonamido)-3-methylenecyclobutylidene)methyl)-4-methylbenzenesulfonamide 
• 1353765-04-4 (Z)-N-(4-fluorobenzyl)-N-((3-methoxy-2-oxabicyclo[4.2.0]octan-8-ylidene)methyl)-4-methylbenzenesulfonamide 
• 1353456-04-8 (Z)-N-(4-fluorobenzyl)-4-methyl-N-((2-(p-tolyl)cyclobutylidene)methyl)benzenesulfonamide 
• 1353455-94-3 (Z)-N-((2-butoxycyclobutylidene)methyl)-N-(4-fluorobenzyl)-4-methylbenzenesulfonamide 
• 1353455-96-5 (Z)-N-(4-fluorobenzyl)-N-((2-methoxy-2-methylcyclobutylidene)methyl)-4-methylbenzenesulfonamide 
• 1353456-06-0 (Z)-N-((2-(4-(tert-butyl)phenyl)cyclobutylidene)methyl)-N-(4-fluorobenzyl)-4-methylbenzenesulfonamide 
• 1353456-02-6 (Z)-N-((2-(4-ethoxyphenyl)cyclobutylidene)methyl)-N-(4-fluorobenzyl)-4-methylbenzenesulfonamide 
• 1353455-85-2 (Z)-tert-butyl 8-((N-(4-fluorobenzyl)-4-methylphenylsulfonamido)methylene)-2-azabicyclo[4.2.0]octane-2-carboxylate 
• 1353455-89-6 (Z)-tert-butyl 7-((N-(4-fluorobenzyl)-4-methylphenylsulfonamido)methylene)-2-azabicyclo[3.2.0]heptane-2-carboxylate 
• 1353455-92-1 (Z)-N-((2-ethoxycyclobutylidene)methyl)-N-(4-fluorobenzyl)-4-methylbenzenesulfonamide 
• 1429612-88-3 (Z)-N-(4-fluorobenzyl)-4-methyl-N-((5-oxo-1-phenyldihydropyrazolo[1,2-a]pyrazol-2(1H,3H,5H)-ylidene)methyl)benzenesulfonamide 

Relevant academic research and scientific papers

Regioselective 1,2-addition of allenamides with: N -haloimides: Synthesis of 2-halo allylic aminal derivatives

A strategy for the synthesis of 2-halo allylic aminal derivatives through regioselective 1,2-addition of allenamides with N-haloimides is presented. This reaction was conducted under very mild conditions and gave up to 99% yield. Moreover, the obtained ha

Enantioselective Synthesis of trans-Vicinal Diamines via Rhodium-Catalyzed [2+2] Cycloaddition of Allenamides

An efficient protocol for the enantioselective Rh-catalyzed intermolecular head-to-head [2+2] cycloaddition of allenamides was developed. A variety of enantio-enriched cyclobutane-1,2-diamine derivatives were achieved in good yields with good to excellent enantioselectivities. (Figure presented.).