102041-34-9

Upstream product

• 102041-38-3 Ethyl-3-(2-allyl-4-methoxyphenyl)-propanoate 
• 53416-46-9 2-(4-methoxyphenyl)-4,4-dimethyl-2-oxazoline 
• 102041-36-1 2-Allyl-4-methoxybenzyl bromide 
• 102041-35-0 2-Allyl-4-methoxybenzyl alcohol 
• 102041-32-7 2-(2-Allyl-4-methoxyphenyl)3-4,4-trimethyl-2-oxazolinium iodide 
• 79928-69-1 2-formyl-5-methoxyallylbenzene 
• 102041-33-8 Ethyl 3-(2-allyl-4-methoxyphenyl)prop-2-enoate 
• 102041-37-2 Ethyl 2-carbethoxy-3-(2-allyl-4-methoxyphenyl)-propanoate 
• 102041-31-6 2-(2-Allyl-4-methoxyphenyl)-4,4-dimethyl-2-oxazoline 

Downstream Products

• 102041-39-4 3-(2-Allyl-4-methoxyphenyl)-1-bromopropane 
• 102041-41-8 N-<3-(2-Allyl-4-methoxyphenyl)-propyl>-5-ethoxy-2-pyrrolidinone 
• 102041-40-7 N-<3-(2-Allyl-4-methoxyphenyl)-propyl>succinimide 

Relevant academic research and scientific papers

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