803725-40-8

Upstream product

• 844-51-9 2,5-diphenyl-p-benzoquinone 
• 803725-38-4 2',3'-diacetoxy-5'-hydroxy-p-terphenyl 
• 20955-74-2 2',3',5'-triacetoxy-p-terphenyl 
• 803725-39-5 2',3'-diacetoxy-5'-benzyloxy-p-terphenyl 

Downstream Products

• 803725-41-9 2'-acetoxy-5'-benzyloxy-3'-hydroxy-p-terphenyl 
• 946489-38-9 4,7-diphenyl-5-benzyloxybenzo[d]-1,3-dioxole 
• 946489-39-0 4,7-diphenylbenzo[d][1,3]dioxol-5-ol 
• 7204-23-1 4,7-diphenyl-1,3-benzodioxol-5,6-dione 
• 803725-43-1 Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-(3',5'-bis-benzyloxy-[1,1';4',1'']terphenyl-2'-yloxy)-tetrahydro-pyran-3-yl ester 
• 1034016-86-8 Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-(3',5'-dihydroxy-[1,1';4',1'']terphenyl-2'-yloxy)-tetrahydro-pyran-3-yl ester 
• 803725-42-0 acetic acid 3',5'-bis-benzyloxy-[1,1';4',1'']terphenyl-2'-yl ester 
• 1026691-86-0 3',5'-dibenzyloxy-2'-hydroxy-p-terphenyl 

Relevant academic research and scientific papers

Syntheses of naturally occurring terphenyls and related compounds

Naturally occurring terphenyls and related compounds such as terferol and its corresponding quinone and phlebiarubrone were synthesized from 2,5-diphenyl-1,4-benzoquinone. According to the proposed biosynthetic pathway, chemical conversion of phlebiarubro

The isolation, structural determination, and total synthesis of terfestatin A, a novel auxin signaling inhibitor from Streptomyces sp.

The structure of terfestatin A was determined to be p-terphenyl β-glucoside on the basis of spectroscopic analyses, chemical degradation, and total synthesis. Indole 3-acetic acid, a plant hormone auxin, regulates every aspects of plant growth and develop