89911-98-8

Upstream product

• 2363-18-0 2'-Amino-2,3-dimethoxydiphenylether-4',5-dicarbonsaeuredimethylester 
• 2363-17-9 2,3-Dimethoxy-2'-nitrodiphenylether-4',5-dicarbonsaeuredimethylester 
• 14719-83-6 methyl 3-nitro-4-chlorobenzoate 
• 118799-01-2 3-<4-(Brommethyl)phenoxy>-4,5-dimethoxybenzylbromid 
• 118799-02-3 <4,5-Dimethoxy-3-<4-(triphenylphosphoniomethyl)phenoxy>benzyl>phosphonium-dibromid 
• 118799-03-4 5-<2-(3-Benzyloxyphenyl)ethenyl>-1-<4-<2-(3-benzyloxyphenyl)ethenyl>phenoxy>-2,3-dimethoxybenzol 
• 118798-99-5 4,5-Dimethoxy-3-<4-(methoxycarbonyl)phenoxy>benzoesaeure-methylester 
• 118799-00-1 3-<4-(Hydroxymethyl)phenoxy>-4,5-dimethoxybenzylalkohol 
• 83011-43-2 3-hydroxy-4,5-dimethoxybenzoate 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 1700-37-4 3-Benzyloxybenzaldehyde 
• 118799-04-5 3-(2-<3-<4-<2-(3-Hydroxyphenyl)ethyl>phenoxy>-4,5-dimethoxyphenyl>ethyl)phenol 

Downstream Products

• 89970-63-8 1,2-Dimethoxy-5-[2-(3-methoxy-phenyl)-ethyl]-3-{4-[2-(3-methoxy-phenyl)-ethyl]-phenoxy}-benzene 
• 118799-05-6 Perrottetin F tetraacetat 

Relevant academic research and scientific papers

Synthesis of bryophyte components. 3. New syntheses of Perrottetines E, F and G

Efficient and expeditious syntheses of the Perrottetines E, F and G (4',5-bis(m-hydroxyphenethyl)diphenyl ether derivatives) are developed, which give rise to these biologically active linear bis(bibenzyl) derivatives on a preparative scale.

Synthesis of Perrottetin F and G, Two Linear Bis(bibenzyl) Ethers from Radula perrottetii.

Perrottetin F and G, two acyclic bis(bibenzyls) with an ether linkage were synthesized using Ulmann and Wittig reactions. - Keywords: Bis(bibenzyl) ether / Perrottetins / Radula perrottetii