17605-05-9

Upstream product

• 17605-04-8 2-(Diacetoxy-methyl)-4,6-diacetoxy-benzoesaeureethylester 
• 74-88-4 methyl iodide 
• 28520-50-5 2,4-Diacetoxy-6-methylbenzoesaeureethylester 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 85565-93-1 2-bromo-3,5-dimethoxy-benzaldehyde 
• 541-41-3 chloroformic acid ethyl ester 
• 134276-82-7 2-(2-bromo-3,5-dimethoxy-phenyl)-[1,3]dioxolane 

Relevant academic research and scientific papers

Asymmetric total synthesis of paecilomycin E, 10′-epi-paecilomycin e and 6′-epi-cochliomycin C

The asymmetric total syntheses of naturally occurring resorcylic acid lactone paecilomycin E and two of its structural congeners have been reported in this article. The major highlight of the synthetic venture is the application of the late stage Mitsunob

C2-symmetrical bipyridyldiols as promising enantioselective catalysts in Nozaki-Hiyama allylation

Several new chiral bipyridyldiol ligands that promote the chromium-catalyzed enantioselective addition of allylic halides to aldehydes in up to 99% ee were synthesized. The chromium-catalyzed allylation of aldehydes using ligands 4 and 4a in the presence