924288-49-3

Upstream product

• 348155-35-1 2-((S)-1-{[2-((S)-1-tert-Butoxycarbonylamino-2-methylcarbamoyl-ethyl)-5-methyl-thiazole-4-carbonyl]-amino}-2-methyl-propyl)-5-methoxymethyl-thiazole-4-carboxylic acid methyl ester 
• 348155-30-6 2-(1-tert-butoxycarbonylamino-2-methylcarbamoylethyl)-5-methylthiazole-4-carboxylic acid methyl ester 
• 348155-31-7 (S)-2-(1-tert-butoxycarbonylamino-2-N-methylcarbamoyl)ethyl-5-methylthiazole-4-carboxylic acid 
• 348155-32-8 methyl 2-[1-(N-Boc)amino-2-methyl]propyl-5-methoxymethylthiazole-4-carboxylate 
• 348155-33-9 2-(1-amino-2-methyl-propyl)-5-methoxymethyl-thiazole-4-carboxylic acid methyl ester 
• 924288-30-2 4-{4-[3-amino-3,6-bis-(4-methoxycarbonyl-thiazol-2-yl)-2,3,4,5-tetrahydro-pyridin-2-yl]-thiazol-2-yl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 924288-20-0 4-{4-[3,6-bis-(4-methoxycarbonyl-thiazol-2-yl)-pyridin-2-yl]-thiazol-2-yl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 924288-34-6 2-(2-tert-butoxycarbonylamino-3-methyl-thiobutyrylamino)-3-(tert-butyl-dimethyl-silanyloxy)-4-methoxy-butyric acid methyl ester 
• 924288-32-4 2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-hydroxy-4-methoxy-butyric acid methyl ester 
• 924288-35-7 2-(2-tert-butoxycarbonylamino-3-methyl-thiobutyrylamino)-3-hydroxy-4-methoxy-butyric acid methyl ester 
• 924288-31-3 2-tert-butoxycarbonylamino-4-methoxy-3-oxo-butyric acid methyl ester 
• 924288-36-8 2-(1-{[2-(1-tert-butoxycarbonylamino-2-methylcarbamoyl-ethyl)-5-methyl-thiazole-4-carbonyl]-amino}-2-methyl-propyl)-5-methoxymethyl-thiazole-4-carboxylic acid 
• 924288-47-1 C₃₇H₃₉N₇O₆S₄Si 
• 924288-33-5 2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-(tert-butyl-dimethyl-silanyloxy)-4-methoxy-butyric acid methyl ester 

Downstream Products

• 924288-58-4 C₅₈H₆₅N₁₃O₁₁S₆Si 
• 924288-59-5 C₅₈H₆₃N₁₃O₁₀S₆Si 
• 924288-60-8 C₅₂H₄₉N₁₃O₁₀S₆ 
• 924288-54-0 C₅₅H₆₀N₁₂O₉S₆Si 

Relevant academic research and scientific papers

Total synthesis of antibiotics GE2270A and GE2270T

(Chemical Equation Presented) Beat the bugs: Total syntheses of the thiopeptide antibiotics GE2270A (X-Y = CH2-CH) and GE2270T (X-Y = CH= C) have been accomplished. The modular approach featured a hetero-Diels-Alder dimerization Circled latin capital letter A to construct the trithiazolyl pyridine domain, and highly regioselective macrolactamizations Circled latin capital letter B to furnish the macrocyclic core.