1399009-21-2

Upstream product

• 1399008-15-1 (2S,2'S)-2,2'-((2-iodo-1,3-phenylene)bis(oxy))bis(propan-1-amine) 
• 1399008-14-0 di-tert-butyl ((2S,2'S)-((2-iodo-1,3-phenylene)bis(oxy))bis(propane-2,1-diyl))dicarbamate 
• 41046-67-7 2-iodoresorcinol 
• 79-21-0 peracetic acid 
• 1399008-27-5 N,N'-(2S,2'S)-2,2'-(2-iodo-1,3-phenylene)bis(oxy)bis(propane-2,1-diyl)bis(2,4,6-trimethylbenzamide) 
• 64-19-7 acetic acid 

Downstream Products

• 1452925-76-6 C₃₀H₃₅IN₂O₄ 
• 1399009-49-4 (S)-7,9-di-tert-butyl-1-oxaspiro[4.5]deca-7,9-diene-2,6-dione 
• 1399008-27-5 N,N'-(2S,2'S)-2,2'-(2-iodo-1,3-phenylene)bis(oxy)bis(propane-2,1-diyl)bis(2,4,6-trimethylbenzamide) 

Relevant academic research and scientific papers

IODOARENE DERIVATIVE, METHOD FOR PRODUCING OPTICALLY ACTIVE SPIROLACTONE COMPOUND USING SAME, AND METHOD FOR PRODUCING OPTICALLY ACTIVE CYCLIZATION ADDUCT

An optically active spirolactone compound is highly enantioselectively produced by using an iodoarene derivative which can be synthesized easily and which is not racemized easily. [Solution] A hypervalent iodine compound precursor (iodoarene derivative) w

Hydrogen bonding and alcohol effects in asymmetric hypervalent iodine catalysis: Enantioselective oxidative dearomatization of phenols

Iodine chooses: A conformationally flexible C2-symmetric organoiodine(III) catalyst for the highly enantioselective catalytic oxidative dearomatization of phenols has been developed. Catalysis is controlled by intramolecular hydrogen-bonding interactions and additional achiral alcohols. Copyright