215440-27-0

Upstream product

• 501-53-1 benzyl chloroformate 
• 58935-08-3 (S)-Amino-[(2R,3R,4R,5R)-3,4-diacetoxy-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-acetic acid methyl ester 
• 58934-96-6 1-(Methyl 2',3'-di-O-acetyl-5'-azido-5'-deoxy-β-D-allofuranosyluronate)uracil 
• 656827-13-3 (R)-benzyl-4-(methoxy(methyl)carbamoyl)-2,2-dimethyloxazolidine-3-carboxylate 
• 656827-14-4 1-[(4R)-3-N-benzyloxycarbonyl-2,2-dimethyl-1,3-oxazolidin-4-yl]-but-3-en-1-one 
• 824411-76-9 (R)-2,2-Dimethyl-4-((2R,3R,4R)-3,4,5-triacetoxy-tetrahydro-furan-2-yl)-oxazolidine-3-carboxylic acid benzyl ester 
• 824411-75-8 (R)-4-((2R,3S,4R)-3,4-Dihydroxy-5-oxo-tetrahydro-furan-2-yl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester 
• 824411-66-7 (4R)-4-[(1'S)-1-acryloyloxy-but-2-enyl]-3-N-benzyloxycarbonyl-2,2-dimethyl-1,3-oxazolidine 
• 824411-67-8 (5S)-5-[(4R)-3-N-benzyloxycarbonyl-2,2-dimethyl-1,3-oxazolidin-4-yl]-2,5-dihydrofuran-2-one 
• 824411-64-5 1-[(4R)-3-N-benzyloxycarbonyl-2,2-dimethyl-1,3-oxazolidin-4-yl]-but-2-en-1-one 
• 824411-77-0 Acetic acid (2R,3R,4R)-4,5-diacetoxy-2-((R)-1-benzyloxycarbonylamino-2-hydroxy-ethyl)-tetrahydro-furan-3-yl ester 

Downstream Products

• 24695-48-5 1-(5'-amino-5'-deoxy-α-D-allofuranuronosyl)uracil 
• 151388-31-7 (S)-Benzyloxycarbonylamino-[(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3,4-dihydroxy-tetrahydro-furan-2-yl]-acetic acid 

Relevant academic research and scientific papers

Complex peptidyl nucleoside antibiotics: Efficient syntheses of the glycosyl nucleoside amino acid cores

Employing an amino acid chiral template strategy, the present research describes a general and highly efficient protocol for the rapid construction of enantiopure furanosyl and pyranosyl nucleoside amino acid cores as present in various complex peptidyl n

Total synthesis of uradl polyoxin c

An improved synthesis of methyl (methyl 5-azido-5deoxy-2,3-O-isopropylidene-β-D-allofuranosid)uronate (7) from methyl 2,3-0-isopropylidene-β-D-rifro-pentodialdo-l,4-furanoside (6), using vinylmagnesium bromide in the key step, and its application to the total synthesis of uracil polyoxin C (1) are described.