120409-52-1

Upstream product

• 141434-45-9 1-[5-(2-Hydroxy-1-methyl-ethyl)-tetrahydro-furan-2-yl]-pentan-2-ol 
• 128806-59-7 (S)-1-[(2S,5R)-5-((S)-2-Hydroxy-1-methyl-ethyl)-tetrahydro-furan-2-yl]-pentan-2-ol 
• 586-75-4 4-chlorobenzoyl chloride 
• 20521-51-1 hexa-4,5-dienal 
• 120341-66-4 (6R,8R)-6,8-Bis-(tert-butyl-dimethyl-silanyloxy)-undeca-1,2-diene 
• 120341-65-3 (S)-2-[(2S,5R)-5-((R)-2-Hydroxy-pentyl)-tetrahydro-furan-2-yl]-propionic acid methyl ester 
• 128806-59-7 (S)-1-[(2S,5R)-5-((R)-2-Hydroxy-1-methyl-ethyl)-tetrahydro-furan-2-yl]-pentan-2-ol 
• 120341-65-3 (R)-2-[(2S,5R)-5-((R)-2-Hydroxy-pentyl)-tetrahydro-furan-2-yl]-propionic acid methyl ester 
• 120341-64-2 2-[(2S,5R)-5-((R)-2-Hydroxy-pentyl)-tetrahydro-furan-2-yl]-acrylic acid methyl ester 
• 120341-63-1 (4R,6R)-Undeca-9,10-diene-4,6-diol 
• 120341-62-0 6-Hydroxy-undeca-9,10-dien-4-one 

Relevant academic research and scientific papers

STRUCTURE OF PAMAMYCIN-607, AN AERIAL MYCELIUM-INDUCING SUBSTANCE OF STREPTOMYCES ALBONIGER

Pamamycin-607 with aerial mycelium-inducing activity has been isolated from Streptomyces alboniger, and its structure with the relative stereochemistry has been determined as a novel ionophore compound (1) on the basis of spectral analysis mainly by 2D 1H-13C and 1H-1H correlation NMR and NOE difference spectroscopy.