193154-23-3

Upstream product

• 169824-26-4 1,2-anhydro-3,4-di-O-benzyl-6-O-trityl-α-D-glucopyranoside 
• 75-05-8 acetonitrile 

Downstream Products

• 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 
• 193154-26-6 N-(fluoren-9-ylmethoxycarbonyl)-2-O-acetyl-3,4-di-O-benzyl-β-D-glucopyranosylamine 
• 193154-30-2 (2S,3S,4S,5R,6R)-5-Acetoxy-3,4-bis-benzyloxy-6-(4,5,6,7-tetrachloro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-tetrahydro-pyran-2-carboxylic acid 
• 193154-29-9 (2S,3S,4S,5R,6R)-5-Acetoxy-3,4-bis-benzyloxy-6-(9H-fluoren-9-ylmethoxycarbonylamino)-tetrahydro-pyran-2-carboxylic acid 
• 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 
• 193154-25-5 N-(fluoren-9-ylmethoxycarbonyl)-2-O-acetyl-3,4-di-O-benzyl-6-O-trityl-β-D-glucopyranosylamine 
• 193154-35-7 Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-6-hydroxymethyl-2-[((2S,3S,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-carbonyl)-amino]-tetrahydro-pyran-3-yl ester 
• 193154-36-8 (2S,3S,4S,5R,6R)-5-Acetoxy-3,4-bis-benzyloxy-6-[((2S,3S,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-carbonyl)-amino]-tetrahydro-pyran-2-carboxylic acid 
• 193154-34-6 Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-[((2S,3S,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-carbonyl)-amino]-6-trityloxymethyl-tetrahydro-pyran-3-yl ester 
• 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 
• 193154-24-4 2-O-acetyl-3,4-di-O-benzyl-6-O-trityl-β-D-glucopyranosylamine 

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