193154-30-2

Upstream product

• 169824-26-4 1,2-anhydro-3,4-di-O-benzyl-6-O-trityl-α-D-glucopyranoside 
• 193154-27-7 Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-(4,5,6,7-tetrachloro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-trityloxymethyl-tetrahydro-pyran-3-yl ester 
• 193154-23-3 (3aS,5R,6R,7S,7aR)-6,7-Bis-benzyloxy-2-methyl-5-trityloxymethyl-5,6,7,7a-tetrahydro-3aH-pyrano[2,3-d]oxazole 
• 193154-24-4 2-O-acetyl-3,4-di-O-benzyl-6-O-trityl-β-D-glucopyranosylamine 
• 117-08-8 tetrachlorophthalic anhydride 
• 193154-28-8 Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-6-hydroxymethyl-2-(4,5,6,7-tetrachloro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-tetrahydro-pyran-3-yl ester 

Downstream Products

• 193154-32-4 Acetic acid (2R,3R,4S,5S,6S)-6-((2R,3R,4S,5R,6R)-3-acetoxy-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-ylcarbamoyl)-4,5-bis-benzyloxy-2-(4,5,6,7-tetrachloro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-tetrahydro-pyran-3-yl ester 

Relevant academic research and scientific papers

Synthesis and biological evaluation of a backbone-modified phytoalexin elicitor

Two suitably protected building blocks (11 and 33) for the preparation of amide-linked heptaglucoside mimetic 2, an analogue of the naturally occurring phytoalexin elicitor 1a, were readily accessible by glycal chemistry. Sequential elongation of terminal