34874-78-7

Upstream product

• 34874-75-4 methyl 4-hydroxy-2-methoxy-3,6-dimethylbenzoate 
• 479-20-9 atranorin 
• 4707-47-5 2,4-dihydroxy-3,6-dimethyl-benzoic acid methyl ester 
• 90685-95-3 pseudocyphellarine A 
• 75-65-0 tert-butyl alcohol 
• 90685-96-4 pseudocyphellarine B 
• 34874-76-5 formyl-3-dihydroxy-4,6-dimethyl-2,5-benzoate de methyle 

Downstream Products

• 34874-80-1 2-hydroxy-4-methoxy-3,5,6-trimethylbenzoic acid 
• 34883-04-0 3-Methoxy-2,4,5-trimethylphenol 
• 90685-96-4 pseudocyphellarine B 
• 111258-37-8 methyl 2,4-di-O-benzyl-2'-methyleriodermate 
• 111258-40-3 methyl 4-O-benzyl-2,2'-di-O-methyleriodermate 
• 34874-83-4 methyl 4-hydroxy-2-methoxy-3,5,6-trimethylbenzoate 
• 34874-82-3 methyl 4-benzyloxy-2-methoxy-3,5,6-trimethylbenzoate 
• 34874-79-8 Methyl-2-hydroxy-4-methoxy-3,5,6-trimethylbenzoat 
• 34874-81-2 methyl 4-benzyloxy-2-hydroxy-3,5,6-trimethylbenzoate 
• 111258-39-0 methyl 2-O-benzyl-4-O-methyleriodermate 
• 90686-03-6 pseudocyphellarin B tetraacetate 
• 20427-81-0 2,4-dihydroxy-3,5,6-trimethylbenzene 
• 111258-36-7 methyl 2,4-di-O-benzyleriodermate 
• 111258-38-9 methyl 4-O-benzyl-2-O-methyleriodermate 

Relevant academic research and scientific papers

Biomimetic Synthesis of Meroterpenoids by Dearomatization-Driven Polycyclization

A biomimetic route to farnesyl pyrophosphate and dimethyl orsellinic acid (DMOA)-derived meroterpenoid scaffolds has yet to be reported despite great interest from the chemistry and biomedical research communities. A concise synthetic route with the poten

206. Synthese des pseudocyphellarines A et B, deux depsides du lichen Pseudocyphellaria endochrysea

The total synthesis of the depsides pseudocyphellarin A ( = 3-hydroxy-4-methoxycarbonyl-2,5,6-trimethylphenyl 3-formyl-2,4-dihydroxy-5,6-dimethylbenzoate; 11) and pseudocyphellarin B (3-hydroxy-4-methoxycarbonyl-2,5,6-trimethylphenyl 2,4-dihydroxy-3-hydro

PSEUDOCYPHELLARINS A AND B, TWO FULLY SUBSTITUTED DEPSIDES FROM THE LICHEN PSEUDOCYPHELLARIA ENDOCHRYSEA

The structures of two fully substituted depsides, pseudocyphellarins A and B, have been elucidated by spectroscopic and chemical methods from the lichen Pseudocyphellaria endochrysea. - Keywords: Pseudocyphellaria endochrysea; Stictaceae; lichen; pseudocy

Synthesis of the Lichen Depsides Pseudocyphellarin A and B

The total synthesis of the fully substituted lichen depsides, pseudocyphellarin A (3-hydroxy-4-methoxycarbonyl-2,5,6-trimethylphenyl 3-formyl-2,4-dihydroxy-5,6-dimethylbenzoate) (1) and pseudocyphellarin B (3-hydroxy-4-methoxycarbonyl-2,5,6-trimethylpheny