1327280-60-3

Upstream product

• 104974-80-3 Acetic acid (2R,3R,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-isocyanato-tetrahydro-pyran-4-yl ester 
• 609367-32-0 ((S)-5-Amino-1-dimethylcarbamoyl-pentyl)-carbamic acid benzyl ester 
• 66118-22-7 (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-isocyanotetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 127812-31-1 (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-formamidotetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 13992-25-1 1-azido-1-deoxy-β-D-glucopyranoside tetraacetate 
• 604-69-3 β-D-glucose pentaacetate 
• 108-24-7 acetic anhydride 
• 2389-60-8 Z-Lys(Boc)-OH 
• 1327280-59-0 C₁₇H₂₆N₄O₄ 
• 241825-30-9 N₂-[(benzyloxy)carbonyl]-N₆-(tert-butoxycarbonyl)-N,N-dimethyl-L-lysinamide 

Relevant academic research and scientific papers

Protecting group free synthesis of urea-linked glycoconjugates: Efficient synthesis of β-urea glycosides in aqueous solution

A method for the protecting group free synthesis of β-urea-linked glycoconjugates has been developed. The one step process, involving reactions between urea and d-glucose, N-acetyl-d-glucosamine or d-xylose in acidic aqueous solution, furnishes the corresponding β-urea glycosides in modest yields. This simple and efficient procedure is applicable to the synthesis of β-urea tethered amino acid-carbohydrate conjugates. This journal is the Partner Organisations 2014.

Synthesis of urea and carbamate glycosides employing unprotected carbohydrates

A study of methods for the synthesis of urea and carbamate glycosides, starting with unprotective carbohydrates, led to the preparation of amino acid-carbohydrate conjugates in aqueous media. Georg Thieme Verlag Stuttgart - New York.