138588-03-1

Upstream product

• 26607-51-2 N-benzyloxycarbonyl-D-alanine 
• 138588-02-0 Acetic acid (2R,3R,4R,5S,6S)-2-((S)-2-amino-propoxy)-4,5-dimethoxy-6-methyl-tetrahydro-pyran-3-yl ester 
• 142739-21-7 2-O-acetyl-3,4-di-O-methyl-α-L-rhamnopyranosyl trichloroacetimidate 
• 683772-92-1 N-benzyloxycarbonyl-D-alaninyl-L-alaninol 
• 138588-01-9 O-(2-O-acetyl-3,4-di-O-methyl-α-L-rhamnopyranosyl)-N-carbobenzyloxy-L-alanilol 
• 25672-82-6 O³,O⁴-dimethyl-α-L-6-deoxy-mannopyranose 
• 683772-91-0 3,4-di-O-acetyl-1,2-O-[(S)-1-(4-pentenyloxy)ethylidene]-β-L-rhamnopyranose 
• 683772-90-9 3,4-di-O-acetyl-1,2-O-[(S)-1-benzyloxyethylidene]-β-L-rhamnopyranose 
• 683773-40-2 1,2-O-[(S)-1-benzyloxyethylidene]-3,4-di-O-methyl-β-L-rhamnopyranose 
• 5158-64-5 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide 
• 142739-20-6 2-O-acetyl-3,4-di-O-methyl-α-L-rhamnopyranose 
• 19914-27-3 N-benzyloxycarbonyl-D-alaninyl-L-alanine methyl ester 
• 683773-35-5 1,2-O-[(S)-1-(4-pentenyloxy)ethylidene]-3,4-di-O-methyl-β-L-rhamnopyranose 
• 138587-99-2 Acetic acid (2S,3R,4R,5S,6S)-2-acetoxy-4,5-dimethoxy-6-methyl-tetrahydro-pyran-3-yl ester 

Downstream Products

• 683773-39-9 (2S)-2-[(N-benzyloxycarbonyl-D-alaninyl)amino]propyl 3,4-di-O-methyl-α-L-rhamnopyranoside 
• 138588-08-6 Acetic acid (2R,3R,4R,5S,6S)-2-((S)-2-{(R)-2-[(2R,3R)-2-((R)-2-acetylamino-3-phenyl-propionylamino)-3-hydroxy-butyrylamino]-propionylamino}-propoxy)-4,5-dimethoxy-6-methyl-tetrahydro-pyran-3-yl ester 

Relevant academic research and scientific papers

Synthesis of the Glycopeptidolipid of Mycobacterium avium Serovar 4: First Example of a Fully Synthetic C-Mycoside GPL

The preparation of the glycopeptidolipid (GPL) present in the cell wall of Mycobacterium avium Serovar 4, namely 3,4-di-O-Me-α-L-Rhap-(1→ 1){R-C21H43CH(OH)CH2CO-D-Phe-[4-O-Me-α -L-Rhap-(1→4)-2-O-Me-α-L-Fucp-(1→3)-α-L-Rhap-

Synthetic studies on the basic glycopeptide structure of C-mycosides

The first synthetic approach towards D-Phe-D-allo-Thr-D-Ala-L-Alanilol-O-(3,4-di-O-Me-Rhap), the glycolipid of C-mycoside is described.