102041-35-0

Upstream product

• 79928-69-1 2-formyl-5-methoxyallylbenzene 
• 53416-46-9 2-(4-methoxyphenyl)-4,4-dimethyl-2-oxazoline 
• 100-09-4 4-methoxybenzoic acid 
• 637038-75-6 C₁₁H₁₂O₃ 
• 1379305-58-4 C₁₁H₁₁ClO₂ 
• 102041-32-7 2-(2-Allyl-4-methoxyphenyl)3-4,4-trimethyl-2-oxazolinium iodide 
• 102041-31-6 2-(2-Allyl-4-methoxyphenyl)-4,4-dimethyl-2-oxazoline 

Downstream Products

• 102041-36-1 2-Allyl-4-methoxybenzyl bromide 
• 681171-45-9 3-methoxy-6-ethyl-phenethyl alcohol 
• 79928-69-1 2-formyl-5-methoxyallylbenzene 
• 57839-47-1 6-methoxy-1-phenyl-3,4-dihydro-1H-isochromene 

Relevant academic research and scientific papers

Direct benzylic C-H activation for C-O bond formation by photoredox catalysis

Power of light: 1,4-dicyanonaphthalene (DCN) and light directly activates benzylic C-H bonds for intra- and intermolecular C-O bond formation. Arylalkyls have also been transformed directly into aryl ketones using water as a source of oxygen. EDG=electron-donating group, EWG=electron-withdrawing group. Copyright

Attempted Synthesis of 13-Aza-7-formyl-3-methoxy-18-nor-8,9-seco-estrone

Oxazoline-directed ortho-lithiation of 1 with n-butyllithium followed by in situ allylation with allyl bromide under N2 affords the oxazoline (II), which on refluxing with iodomethane yields the methiodide (III).This on reduction with NaBH4 followed by ac