761457-29-8

Upstream product

• 25576-97-0 2,3,6-trimethoxytoluene 
• 1760-80-1 2-methoxy-3-methylbenzene-1,4-diol 

Downstream Products

• 761457-37-8 1-(4-methoxy-2,5-bis-methoxymethoxy-3-methyl-phenyl)-3-methyl-butan-2-ol 
• 1209497-66-4 C₃₅H₅₀O₇Si 
• 622852-28-2 2,5-dihydroxy-4-methoxy-3-methyl-benzaldehyde 
• 1189524-42-2 (S,E)tert-butyl(6-(4-methoxy-2,5-bis(methoxymethoxy)-3-methylphenyl)-4-methylhex-5-enyloxy)diphenylsilane 
• 777858-58-9 2-methoxy-1,4-bis(methoxymethoxy)-3-methylbenzene 
• 638188-73-5 (2S)-1-(2-((2S,4S)-5-(tert-butyldiphenylsilyloxy)-4-methylpentan-2-yl)-6-methoxy-5-(methoxymethoxy)-7-methylbenzofuran-4-yl)-2-((4R,5S,6R)-2,2,5-trimethyl-6-((S)-3-methylpent-4-enyl)-1,3-dioxan-4-yl)propan-1-ol 
• 638188-75-7 2-((2S,4S)-5-(tert-butyldiphenylsilyloxy)-4-methylpentan-2-yl)-4-((2R,3R,4S,5R,6R)-4-hydroxy-3,5-dimethyl-6-((S)-3-methylpent-4-enyl)tetrahydro-2H-pyran-2-yl)-6-methoxy-7-methylbenzofuran-5-ol 
• 638188-67-7 (3S,5S)-6-(tert-Butyl-diphenyl-silanyloxy)-1-(4-methoxy-2,5-bis-methoxymethoxy-3-methyl-phenyl)-3,5-dimethyl-hexan-2-ol 
• 638188-69-9 tert-Butyl-[(2S,4S)-4-(6-methoxy-5-methoxymethoxy-7-methyl-benzofuran-2-yl)-2-methyl-pentyloxy]-diphenyl-silane 
• 638188-68-8 2-[(1S,3S)-4-(tert-Butyl-diphenyl-silanyloxy)-1,3-dimethyl-butyl]-6-methoxy-7-methyl-benzofuran-5-ol 
• 761457-30-1 1-(4-methoxy-2,5-bis-methoxymethoxy-3-methyl-phenyl)-3-methyl-butan-2-one 
• 638188-66-6 C₁₂H₁₇BrMgO₅ 

Relevant academic research and scientific papers

Synthesis of polyfluoroalkyl aza-polycyclic aromatic hydrocarbons enabled by addition of perfluoroalkyl radicals onto vinyl azides

Radical perfluoroalkylation of α-(biaryl-2-yl)vinyl azides is capable of supplying polyfluoroalkyl aza-polycyclic aromatic hydrocarbons (aza-PAHs). Commercially available Me3SiRf (Rf = CF 3, C2F5

A short access to the skeleton of elisabethin a and formal syntheses of elisapterosin B and colombiasin A

A short stereoselective synthesis of the Elisabethin A skeleton 4 is described, which opens a formal access to the diterpenes Elisapterosin B and Colombiasin A as well. Key reactions were an intermolecular endo-selective Diels-Alder reaction to generate t

A Novel Approach toward the Synthesis of Kendomycin: Selective Synthesis of a C-Aryl Glycoside as a Single Atropisomer

(Matrix presented) A convergent and concise route to an advanced precursor 2b of kendomycin (1) has been developed by applying a SN1 ring cyclization as a key step. The resulting C-aryl glycoside was initially isolated as a rotameric mixture, b