79130-37-3

Upstream product

• 646-25-3 diaminodecane 
• 98-59-9 p-toluenesulfonyl chloride 
• 201230-82-2 carbon monoxide 
• 70-55-3 toluene-4-sulfonamide 
• 3710-30-3 1,7-Octadiene 
• 4101-68-2 1,10-dibromodecane 

Downstream Products

• 87338-11-2 1,12-bis(p-tolylsulfonyl)-1,12-diazacyclodocosane 
• 81506-03-8 4,15-bis(p-tolylsulfonyl)-4,15-diazaoctadecane-1,18-diol 
• 130945-22-1 N,N'-di-p-toluenesulfonyl-N,N'-bis<10-(p-toluenesulfonyloxy)decyl>-1,10-decanediamine 
• 130945-18-5 N,N'-bis(10-hydroxydecyl)-N,N'-di-p-toluenesulfonyl-1,10-decanediamine 
• 120615-14-7 N,N'-bis(10-bromodecyl)-N,N'-di-p-toluenesulfonyl-1,10-decanediamine 
• 120590-13-8 1,12,23,34-tetra-p-toluenesulfonyltetraazacyclotetratetracontane 
• 81506-06-1 N,N',4,15-tetrakis(p-tolylsulfonyl)-4,15-diazaoctadecane-1,18-diamine 
• 81522-67-0 4,15-bis(p-tolylsulfonyl)-4,15-diazaoctadecane-1,18-diyl bis(methanesulfonate) 
• 81506-05-0 4,15-bis(p-tolylsulfonyl)-4,15-diazaoctadecane-1,18-diamine 
• 81506-08-3 1,5,9,20,24,28-hexakis(p-tolylsulfonyl)-1,5,9,20,24,28-hexaazacyclooctatriacontane 
• 277760-15-3 N¹,N⁵,N¹⁶,N²⁰-tetra(p-toluenesulfonyl)-1,20-bis(ethylamino)-5,16-diazaeicosane 
• 277760-06-2 N¹,N⁵,N¹⁶,N²⁰-tetra(p-toluenesulfonyl)-1,20-diamino-5,16-diazaeicosane 
• 278807-31-1 C₃₄H₅₄N₄O₆S₂ 
• 81506-04-9 4,15-bis(p-tolylsulfonyl)-4,15-diazaoctadecane-1,18-dinitrile 

Relevant academic research and scientific papers

A novel rhodium-catalyzed domino-hydroformylation-reaction for the synthesis of sulphonamides

An efficient and highly selective method for the synthesis of sulphonamides by a domino hydroformylation-reductive sulphonamidation reaction has been developed. Various olefins and sulphonamides are converted into the desired products in good yields and with excellent selectivities in the presence of a rhodium/Naphos catalyst. This journal is

Convenient synthesis of large tetraazamacrocycles bearing alkylene, cyclophane and crown ether type skeletons

A series of large tetraazamacrocycles with 28- to 44-membered rings consisting of alkylene, phenylene or ether type backbones has been prepared without the use of high-dilution conditions in practically significant yields (25-42%). The reaction can be car

Synthesis of Large Macrocyclic Tetraaza Compounds with A Methylene Backbone: Cyclo4, (n = 6,7,8,9 and 10). The Formation of 28-, 32-, 36-, 40- and 44-Membered Rings.

A series of macrocyclic tetraamines with 28-, 32-, 36-, 40- and 44-membered rings have been efficiently prepared from the corresponding ditosylamide and monobromoalcohol derivatives in 6 steps via a double condensation reaction.Overall yields were: 41, 41, 46, 29, and 33 percent, respectively, for 1,8,15,22-tetraazacyclooctacontane (11a), 1,9,17,25-tetraazacyclodotriacontane (11b), 1,10,19,28, tetraazacyclohexatriacontane (11c), 1,11,21,31-tetraazacyclotetracontane (11d) and 1,12,23,34-tetraazacyclotetratetracontane (11e).

Anion Coreceptor Molecules. Linear Molecular Recognition in the Selective Binding of Dicarboxylate Substrates by Ditopic Polyammonium Macrocycles

Three macrocyclic hexaamines 1,2, and 4 and the acyclic tetraamine 5 and hexaamine 6 have been synthesized.The hexaamines 1, 2, and 4 are ditopic coreceptor molecules containing two triamine subunits which may bind anionic substrates when protonated.The s

Preferential Introduction of a Pyridylmethyl Group into Sulfonamides as an Approach to an Intramolecular Transimination

N,N'-Bis(p-tolylsulfonyl)-α,ω-alkanediamine disodium salts (n=3, 4, 5, 6, 7, 8, 9, 10) were subjected to monopyridylmethylation by the reaction with 5'-deoxy-5'-chloro- or 5'-deoxy-2'-chloro-3,4'-O-isopropylidenepyridoxine hydrochloride, accompanied by th