473710-39-3

Upstream product

• 473710-01-9 [(S)-3-Methyl-1-(3-oxo-propylcarbamoyl)-butyl]-carbamic acid benzyl ester 
• 473709-93-2 (2S,3R)-2-Amino-3-{(2R,3R,4R,5R)-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester 
• 94226-56-9 tert-butyl 2-(dibenzylamino)ethanoate 
• 1197388-81-0 C₁₇H₂₇N₃O₃*ClH 
• 1197388-84-3 C₃₅H₅₆N₂O₉Si₂ 
• 473709-91-0 (2S,3R)-3-{(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-2-dibenzylamino-3-hydroxy-propionic acid tert-butyl ester 
• 473710-00-8 [(S)-1-(3,3-Diethoxy-propylcarbamoyl)-3-methyl-butyl]-carbamic acid benzyl ester 
• 137233-53-5 2',3'-O-bis(tert-butyldimethylsilyl)-3-N-(p-methoxybenzyl)uridine-5'-aldehyde 

Downstream Products

• 473710-93-9 (2S,3R)-2-[3-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-propylamino]-3-{(2R,3S,4R,5R)-3,4-dihydroxy-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester 
• 473710-40-6 2-[3-(2-amino-4-methyl-pentanoylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester 
• 473710-41-7 (2S,3R)-2-[3-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-propylamino]-3-[(2R,3R,4R,5R)-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-3-hydroxy-propionic acid tert-butyl ester 
• 473710-95-1 (2S,3R)-2-[3-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-propylamino]-3-{(2R,3S,4R,5R)-3,4-dihydroxy-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid 
• 473710-64-4 C₅₆H₉₈N₁₀O₁₄Si₂ 
• 473710-63-3 C₆₃H₁₀₃N₁₁O₁₆Si₂ 

Relevant academic research and scientific papers

Improved convergent synthesis of 5'-epi-analogues of muraymycin nucleoside antibiotics

Nucleoside antibiotics represent a promising class of natural products for the development of novel antibacterial agents, with particular respect to structurally simplified analogues maintaining biological activity. There are established truncated 5-epi-d

Muraymycins, novel peptidoglycan biosynthesis inhibitors: Synthesis and SAR of their analogues

A series of Muraymycin analogues was synthesized. These analogues showed excellent antimicrobial activity against gram-positive organisms. These analogues also showed excellent inhibitory activity against the target peptidoglycan biosynthesis enzyme MraY,