1361331-91-0

Upstream product

• 1361331-82-9 (S)-1-(methoxymethoxy)-2-(2-methylbutyl)benzene 
• 1609-86-5 Tert-butyl isocyanate 
• 29394-58-9 (S)-1-iodo-2-methyl-butane 
• 68314-54-5 1-bromo-2-(methoxymethoxy)benzene 
• 534-00-9 (S)-2-methylbutyl bromide 

Downstream Products

• 1361332-13-9 N-tert-butyl-6-((S)-2,4-dihydroxybutyl)-2-hydroxy-3-((S)-2-methylbutyl)benzamide 
• 1361332-15-1 N-tert-butyl-6-((R)-2,4-dihydroxybutyl)-2-hydroxy-3-((S)-2-methylbutyl)benzamide 
• 1361332-06-0 N-tert-butyl-6-[(R)-4-(tert-butyldimethylsilyloxy)-2-hydroxybutyl]-2-(methoxymethoxy)-3-((S)-2-methylbutyl)benzamide 
• 1361331-98-7 N-tert-butyl-6-[(S)-4-(tert-butyldimethylsilyloxy)-2-hydroxybutyl]-2-(methoxymethoxy)-3-((S)-2-methylbutyl)benzamide 
• 1399799-99-5 C₄₉H₇₇NO₉Si₂ 
• 1399800-95-3 C₄₀H₇₁NO₆SSi₂ 
• 1399800-93-1 C₄₀H₇₁NO₆SSi₂ 

Relevant academic research and scientific papers

Total synthesis of a noricumazole A library and evaluation of HCV inhibition

The total synthesis of 16 new ion channel inhibitors derived from noricumazole A, a secondary metabolite from the myxobacterium Sorangium cellulosum, is reported. Particular focus of library design is put on stereochemical permutations in the central regi

Isolation and total synthesis of icumazoles and noricumazoles-antifungal antibiotics and cation-channel blockers from Sorangium cellulosum

Joint efforts: The antifungal icumazole A, the potassium-ion-channel inhibitor noricumazole A, and their glycosylated derivatives are new, structurally related secondary metabolites isolated from Sorangium cellulosum. Their structures have been fully assi