334536-41-3

Upstream product

• 334536-13-9 (2-hydroxy-ethyl) 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside 
• 334536-00-4 allyl 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside 
• 334535-96-5 allyl 2,3-di-O-benzyl-α-D-xylopyranoside 
• 140420-69-5 allyl α-D-xylopyranoside 
• 100-39-0 benzyl bromide 
• 5292-43-3 bromoacetic acid tert-butyl ester 
• 107-10-8 propylamine 
• 334536-27-5 (2-bromo-ethyl) 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside 

Downstream Products

• 334536-55-9 (N-(tert-butoxycarbonyl)-2-propylamino-ethyl) 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside 

Relevant academic research and scientific papers

Design, synthesis and preliminary biological evaluation of a focused combinatorial library of stereodiverse carbohydrate-scaffold-based peptidomimetics

A focused combinatorial library of 126 mimetics of the RGD sequence based on sugar scaffolds have been rationally constructed using molecular modeling, with a particular emphasis on the stereodiversity of the library. A liquid phase, mix and divide synthesis was used, active compounds being identified by using orthogonal libraries and recursive deconvolution strategies.