7572-90-9

Upstream product

• 81581-25-1 ethyl 2-(4-benzyloxy-3-methoxybenzoyl)acetoacetate 
• 1486-53-9 4-(benzyloxy)-3-methoxybenzoic acid 
• 1486-52-8 3-methoxy-4-benzyloxybenzoyl chloride 
• 60525-32-8 ethyl 3-[4-(benzyloxy)-3-methoxyphenyl]-3-oxopropanoate 

Downstream Products

• 98314-80-8 ethyl 2-<4-formyl-2-(methoxymethoxy)phenoxy>-3-(4-benzyloxy-3-methoxyphenyl)-3-oxopropionate 
• 99442-72-5 3-(4-Benzyloxy-3-methoxy-phenyl)-2-(8-hydroxy-6-methoxy-2-oxo-2H-chromen-7-yloxy)-3-oxo-propionic acid ethyl ester 
• 99430-18-9 3-(4-Benzyloxy-3-methoxy-phenyl)-2-(7-hydroxy-6-methoxy-2-oxo-2H-chromen-8-yloxy)-3-oxo-propionic acid ethyl ester 
• 4687-40-5 diethyl 2,3-bis-(3,4-dimethoxybenzoyl)butane-1,4-dioate 
• 96931-98-5 diethyl 2,3-bis-(4-benzyloxy-3-methoxybenzoyl)butane-1,4-dioate 
• 90706-59-5 cleomiscosin A diacetate 
• 102070-25-7 8-[(1R,2S)-2-(4-Benzyloxy-3-methoxy-phenyl)-2-hydroxy-1-hydroxymethyl-ethoxy]-7-hydroxy-6-methoxy-chromen-2-one 
• 102070-25-7 8-[(1R,2R)-2-(4-Benzyloxy-3-methoxy-phenyl)-2-hydroxy-1-hydroxymethyl-ethoxy]-7-hydroxy-6-methoxy-chromen-2-one 
• 76948-72-6 cleomiscosin A 
• 102070-27-9 Acetic acid 8-[(1R,2S)-2-acetoxy-1-acetoxymethyl-2-(4-benzyloxy-3-methoxy-phenyl)-ethoxy]-6-methoxy-2-oxo-2H-chromen-7-yl ester 
• 102070-27-9 Acetic acid 8-[(1R,2R)-2-acetoxy-1-acetoxymethyl-2-(4-benzyloxy-3-methoxy-phenyl)-ethoxy]-6-methoxy-2-oxo-2H-chromen-7-yl ester 
• 102070-29-1 cleomiscosin A monoacetate 
• 22888-70-6 (+/-)-silybin 
• 98314-88-6 {3-[(2R,3R)-2-Hydroxymethyl-3-(3-methoxy-4-methoxymethoxy-phenyl)-2,3-dihydro-benzo[1,4]dioxin-6-yl]-oxiranyl}-(2,4,6-tris-methoxymethoxy-phenyl)-methanone 

Relevant academic research and scientific papers

An efficient and flexible synthesis of model lignin oligomers

The use of model compounds in the development of selective lignin depolymerisation processes has been limited by the lack of complexity of these models compared with lignin itself. In this paper we report a convergent and efficient synthetic method for th

Synthesis and N.m.r. Spectra of 2,6- and 2,4-Diaryl-3,7-dioxabicyclooctanes

A series of isomeric 2,6- and 2,4-diaryl-3,7-dioxabicyclooctanes have been prepared via the corresponding threo, and erythro-dioxo-diesters.Comparison of their 1H and 13C n.m.r. spectra reveals small differences in chemical shifts and coupling constants which could be diagnostic in assigning structures to such compounds.The structure of 4-hydroxysesamin has been confirmed by direct correlation with sesamin.