78631-98-8

Upstream product

• 1655-07-8 ethyl 2-oxocyclohexane carboxylate 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 4746-93-4 1,4-dioxaspiro[4.5]decane-6-carboxylic acid 
• 73232-76-5 15,16-Dimethoxy-8-oxo-B-nor-cis-erythrian-6α-carbonsauere 
• 78632-14-1 1-<(2,2-Ethylendioxy)cyclohexyl>-3,4-dihydro-6,7-dimethoxyisochinolin 
• 78632-11-8 N-<2-(3,4-Dimethoxyphenyl)ethyl>-2,2-ethylendioxy-1-cyclohexancarboxamid 

Downstream Products

• 78632-17-4 7-(2-<2-(Acetylamino)ethyl>-4,5-dimethoxyphenyl)-7-oxoheptansaeure-methylester 
• 78632-06-1 (E)-2-<2-Acetyl-3,4-dihydro-6,7-dimethoxy-1(2H)-isochinolinyliden>cyclohexanon 
• 78632-05-0 (Z)-2-<2-Acetyl-3,4-dihydro-6,7-dimethoxy-1(2H)-isochinolinyliden>cyclohexanon 
• 78632-08-3 2-(6,7-Dimethoxy-1-isochinolinyl)phenol 
• 78632-07-2 6,7-Dimethoxy-1-isochinolinhexansauere 
• 78632-09-4 2-(6,7-Dimethoxy-1-isochinolinyl)cyclohexanon 
• 78632-10-7 6,7-Dimethoxy-1-isochinolinhexansauere-methylester 

Relevant academic research and scientific papers

A Reversible Rearrangement of the trans-Erythrinane Ring System, IV. Ivestigations Concerning the Reaction Mechanism

The labelled β-lactame carboxylic acid 10a is prepared via the diol-A 7.The products of thermal decarboxylation 11a and 12a include the whole activity of the original carboxylic acid 10a.On the other hand, decarboxylation of 10a with sulfuric ac