27722-61-8

Upstream product

• 59276-90-3 2,3,4'-Trimethoxybibenzyl 
• 86-51-1 2,3-dimethyoxybenzaldehyde 
• 105-13-5 4-Methoxybenzyl alcohol 
• 5653-67-8 2,3-dimethoxybenzyl alcohol 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 17105-65-6 dimethyl 4-methoxybenzylphosphonate 
• 2011-06-5 2-benzyloxy-3-methoxybenzaldehyde 
• 58698-98-9 2,3,4'-Trihydroxybibenzyl 
• 77-78-1 dimethyl sulfate 
• 158751-23-6 2-Benzyloxy-1-methoxy-3-[(E)-2-(4-methoxy-phenyl)-vinyl]-benzene 

Downstream Products

• 158751-24-7 3-{2-Methoxy-6-[2-(4-methoxy-phenyl)-ethyl]-phenoxy}-benzaldehyde 
• 27722-63-0 2-Ethoxy-3-methoxy-4'-methoxydihydrostilben 
• 158751-26-9 [3-(2-(Tetrahydro-pyran-2-yloxy)-6-{2-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-ethyl}-phenoxy)-benzyl]-phosphonic acid dimethyl ester 
• 246257-37-4 C₃₁H₃₅BrO₅ 
• 158751-25-8 2-(3-Bromomethyl-phenoxy)-3-[2-(4-hydroxy-phenyl)-ethyl]-phenol 
• 246257-34-1 2-[3-(hydroxymethyl)phenoxy]-3-[2-(4-hydroxyphenyl)ethyl]phenol 

Relevant academic research and scientific papers

Bibenzyl derivatives from Pellia epiphylla

Reinvestigation of the phenolic constituents from a diethyl ether extract of gametophytes of Pellia epiphylla yielded pellepiphyllin, 7- hydroxypellepiphyllin, perrottetin E, perrottetin E-11-methyl ether, 14'- hydroxyperrottetin E, 10'-hydroxyperrottetin E, 10'-hydroxyperrottetin E-11- methyl ether, 10,10'-dihydroxyperrottetin E and 13',13'''-bis(10'- hydroxyperrottetin E). The structures of three bisbibenzyls published earlier are revised. The new structures have been elucidated by two-dimensional NMR- techniques and chemical synthesis. In contrast to previous publications, pellepiphyllin has been found as a constituent of P. epiphylla.

Structures and total synthesis of two novel bis(bibenzyls), paleatins A and B, from the liverwort Marchantia paleacea var. diptera

Two novel bis(bibenzyls) named paleatins A (1) and B (2) have been isolated from the liverwort, Marchantia paleacea var. diptera. Their structures have been established by a combination of high-resolution NMR spectra and chemical degradation. A total synt