35354-34-8

Upstream product

• 2150-46-1 Methyl 2,5-dihydroxybenzoate 
• 75-36-5 acetyl chloride 
• 1084-96-4 2,5-bis(acetyloxy)benzoic acid 
• 490-79-9 2,5-dihydroxybenzoic acid. 
• 186581-53-3 diazomethane 
• 5330-25-6 5-O-Acetylgentisinsaeure 

Downstream Products

• 35354-35-9 Methyl-3-chlor-5-acetoxysalicylat 
• 32744-80-2 2-chloro-6-(hydroxymethyl)benzene-1,4-diol 
• 108124-72-7 2-β-D-glucopyranosyloxy-5-hydroxy-benzoic acid methyl ester 
• 91738-41-9 5-<<2-O-(2,3,5-O-Acetyl-β-D-apiofuranosyl)-3-O-benzyl-4,6-O-benzyliden-β-D-glucopyranosyl>oxy>-2-hydroxybenzoesaeure-methylester 
• 91738-42-0 5-[(2S,3R,4S,5S,6R)-3-((2S,3R,4S)-3,4-Diacetoxy-4-acetoxymethyl-tetrahydro-furan-2-yloxy)-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy]-2-hydroxy-benzoic acid methyl ester 
• 91738-31-7 2-Benzyloxy-5-<(2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranosyl)oxy>benzoesaeure-methylester 
• 91738-33-9 5-<(3-O-Benzyl-4,6-O-benzyliden-β-D-glucopyranosyl)oxy>-2-benzyloxybenzoesaeure-methylester 
• 91738-32-8 5-<(3-O-Benzyl-β-D-glucopyranosyl)oxy>-2-benzyloxybenzoesaeure-methylester 
• 67454-60-8 5-<<2-O-(β-D-Apiofuranosyl)-β-D-glucopyranosyl>oxy>-2-hydroxybenzoesaeure 
• 91738-30-6 2-O-Benzylgentisinsaeure-methylester 
• 91738-29-3 2-O-Benzyl-5-O-acetylgentisinsaeure-methylester 
• 115486-82-3 5-acetoxy-2-(tetra-O-acetyl-β-D-glucopyranosyloxy)-benzoic acid methyl ester 

Relevant academic research and scientific papers

Enantioselective Lactonization by π-Acid-Catalyzed Allylic Substitution: A Complement to π-Allylmetal Chemistry

Asymmetric allylic alkylation (AAA) is a powerful method for the formation of highly useful, non-racemic allylic compounds. Here we present a complementary enantioselective process that generates allylic lactones via π-acid catalysis. More specifically, a

Synthesis of the First Leaf Movement Factor from Mimosa pudica L.

In the following we describe the synthesis of the first Leaf Movement Factor from Mimosa pudica L.(M-LMF 1).Proceeding from functionalized derivatives of 2,5-dihydroxybenzoic acid (gentisic acid) and D-glucose we obtained by Koenigs-Knorr reaction the pro