321658-88-2

Upstream product

• 34753-62-3 N-Benzylbis(3-chloropropyl)amine 
• 321658-87-1 N-tert-butoxycarbonyl bis(2-thioethyl)amine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 321658-86-0 N-tert-butoxycarbonyl bis(2-thioacetoxyethyl)amine 
• 118753-70-1 N-(tert-butyloxycarbonyl)bis(2-chloroethyl)amine 

Downstream Products

• 321659-09-0 11-[3-(4-tert-butoxycarbonyl-1,7-dithia-4,11-diaza-cyclotetradec-11-ylmethyl)-benzoyl]-1,4,8,11tetraaza-cyclotetradecane-1,4,8-tricarboxylic acid tri-tert-butyl ester 
• 321659-05-6 11-[4-(4-tert-butoxycarbonyl-1,7-dithia-4,11-diaza-cyclotetradec-11-ylmethyl)-benzoyl]-1,4,8,11tetraaza-cyclotetradecane-1,4,8-tricarboxylic acid tri-tert-butyl ester 
• 321659-06-7 [4-(1,7-Dithia-4,11-diaza-cyclotetradec-11-ylmethyl)-phenyl]-(1,4,8,11-tetraaza-cyclotetradec-1-yl)-methanone 
• 321659-10-3 [3-(1,7-Dithia-4,11-diaza-cyclotetradec-11-ylmethyl)-phenyl]-(1,4,8,11-tetraaza-cyclotetradec-1-yl)-methanone 

Relevant academic research and scientific papers

New heteroditopic, linked macrocyclic systems derived from selectively protected N2S2-, N3O2- and N4-donor macrocycles

The use of selectively tert-butoxycarbonyl protected derivatives of 1,9-dithia-5,13-diazacyclohexadecane 1, 1,7-dithia-4,11-diazacyclotetradecane 2, 1,4,8,11-tetraazacyclotetradecane 3 and 2,5-dioxa-8,11,14-triaza-1,6(1,2)dibenzenacyclopentadecaphane 4 has enabled the efficient synthesis of new linked heteroditopic macrocyclic systems incorporating combinations of N2S2- and N4- or N3O2-donor sites. Incorporation of two types of binding sites in the respective products makes them suitable candidates for the synthesis of a range of mixed-metal, di- and oligo-nuclear metal complexes.