717-41-9

Upstream product

• 100-39-0 benzyl bromide 
• 130490-23-2 1,2,6-thiadiazine 1,1-dioxide potassium salt 

Downstream Products

• 130490-30-1 2-benzyl-4-chloro-1,2,6-thiadiazine 1,1-dioxide 
• 130490-31-2 2-benzyl-4-bromo-1,2,6-thiadiazine 1,1-dioxide 
• 130490-32-3 2-benzyl-4-iodo-1,2,6-thiadiazine 1,1-dioxide 
• 130506-20-6 2-benzyl-4-vinyl-1,2,6-thiadiazine 1,1-dioxide 
• 130506-19-3 2-benzyl-4-chloro-5-methyl-1,2,6-thiadiazine 1,1-dioxide 
• 130490-43-6 2-benzyl-4-bromo-5-methyl-1,2,6-thiadiazine 1,1-dioxide 
• 130490-47-0 2-benzyl-4-phenyl-1,2,6-thiadiazine 1,1-dioxide 
• 130490-37-8 2-benzyl-4-chloro-5,6-dihydro-5-methyl-1,2,6-thiadiazine 1,1-dioxide 
• 130490-38-9 2-benzyl-4-bromo-5,6-dihydro-5-methyl-1,2,6-thiadiazine 1,1-dioxide 
• 130490-48-1 2-benzyl-4-(2-thienyl)-1,2,6-thiadiazine 1,1-dioxide 
• 130490-34-5 2-benzyl-4,4-dichloro-trans-3,5-dimethoxy-3,4,5,6-tetrahydro-1,2,6-thiadiazine 1,1-dioxide 
• 130490-44-7 2-benzyl-4-chloro-5-phenyl-1,2,6-thiadiazine 1,1-dioxide 
• 130490-45-8 2-benzyl-4-bromo-5-phenyl-1,2,6-thiadiazine 1,1-dioxide 
• 130490-49-2 2-benzyl-4-phenylethynyl-1,2,6-thiadiazine 1,1-dioxide 

Relevant academic research and scientific papers

Construction of Chiral 1,3-Diamines through Rhodium-Catalyzed Asymmetric Arylation of Cyclic N-Sulfonyl Imines

A rhodium/sulfur-olefin complex catalyzed asymmetric 1,2-addition of arylboronic acids to six-membered 1,2,6-thiadiazinane 1,1-dioxide-type cyclic imines to access highly optically active sulfamides (95-99% ee) has been developed. By taking advantage of t

Organometallics in Carbon-Carbon Bond Formation in 1,2,6-Thiadiazine 1,1-Dioxides

Carbon substituents have been introduced exclusively into the electrophilic 5-position in 1,2,6-thiadiazine 1,1-dioxides by 1,1-adduct formation with organomagnesium reagents followed by reoxidation by manganese dioxide to the conjugated, 5-substituted heterocycle.Pd(II)-catalyzed coupling reactions between organostannanes and the 4-bromo of 4-iodo derivatives have been used for the introduction of a 4-carbon substituent.Methods for chlorination, bromination or iodination in the 4-position are described.