223704-16-3

Upstream product

• 186144-56-9 N-[(1R,2R)-2-(2-Methoxycarbonyl-acetylamino)-cyclohexyl]-malonamic acid methyl ester 
• 98-59-9 p-toluenesulfonyl chloride 
• 10027-80-2 (1R,2R)-1,2-dicyclohexane-1,2-diamine dihydrochloride 
• 143585-47-1 (R,R)-1,2-bis(tosylamino)cyclohexane 
• 852043-14-2 C₆₄H₆₆N₂O₆S₂ 
• 627-18-9 1-bromo-3-propanol 

Downstream Products

• 223704-18-5 (R,R)-N,N'-(cyclohexane-1,2-diyl)bis-<3-(p-toluenesulphonylamino)propyl methanesulphonate> 

Relevant academic research and scientific papers

Conformationally biased selective alkylation of trans-cyclohexane-1,2- bis(sulfonamide) assisted by solvent-tuned protecting groups: Applications to the synthesis of a large optically active polyazamacrocycle

The selective alkylation of (R,R)-cyclohexane-1,2-bis(sulfonamide) with trityl bromoalkyl ethers has been studied in detail. The major formation of either mono- or dialkylated compounds clearly depends on the right combination of protecting groups and the

Chemoenzymatic syntheses of two optically active hexa-azamacrocycles

Two optically active hexa-azamacrocycles with C2 and D2 symmetry, respectively, have been efficiently synthesized from the enzymatically prepared (R,R)-cyclohexane-1,2-diamine bis(amidoester) derivative (R,R)-4.