860303-52-2

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 917-54-4 methyllithium 
• 155976-02-6 methyl (2R)-N-(4-methylphenyl)sulfonylaziridine-2-carboxylate 

Downstream Products

• 860303-50-0 (R)-2-(2-Methyl-[1,3]dioxolan-2-yl)-1-(toluene-4-sulfonyl)-aziridine 
• 1553423-27-0 4-methyl-N-(((1S,2R,5S)-3-oxo-8-oxabicyclo[3.2.1]oct-6-en-2-yl)methyl)benzenesulfonamide 
• 1553423-28-1 4-methyl-N-(((1R,2R,5R)-3-oxo-8-oxabicyclo[3.2.1]oct-6-en-2-yl)methyl)benzenesulfonamide 
• 860303-49-7 (+)-N-[(1R)-2-{2-[(2S,5S,6S)-2-(tert-butyldimethylsilanyloxy)-5-(tert-butyldiphenylsilanyloxy)-6-methyloct-7-enyl]-(1,3-dithian-2-yl)}-1-(2-methyl-1,3-dioxolan-2-yl)-ethyl]4-methylbenzenesulfonamide 
• 860303-62-4 N-[(R)-2-[2-((2S,5S,6S)-2,5-Dihydroxy-6-methyl-oct-7-enyl)-[1,3]dithian-2-yl]-1-(2-methyl-[1,3]dioxolan-2-yl)-ethyl]-4-methyl-benzenesulfonamide 

Relevant academic research and scientific papers

Total synthesis of the neotropical poison-frog alkaloid (-)-205B

(Chemical Equation Presented) A stereocontrolled total synthesis of the neotropical poison-frog alkaloid (-)-205B (1) has been achieved, employing a dithiane three-component linchpin coupling, a one-pot sequential construction of the embedded indolizidine

A general, convergent strategy for the construction of indolizidine alkaloids: Total syntheses of (-)-indolizidine 223AB and alkaloid (-)-205B

N-Toluenesulfonyl aziridines comprise effective second electrophiles in the solvent controlled three-component linchpin union of silyl dithianes for the stereocontrolled convergent elaboration of protected 1,5-amino alcohols. This tactic, in conjunction w