173383-18-1

Upstream product

• 173383-04-5 Acetylamino-(3,5-dimethoxy-phenyl)-acetic acid 
• 123418-41-7 N-t-butoxycarbonyl-3,5-dichloro-L-tyrosine 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 123593-66-8 L-N-(tert-butoxycarbonyl)-4-benzyloxyphenylglycine 
• 173383-17-0 (S)-[(S)-2-Amino-3-(3,5-dichloro-4-hydroxy-phenyl)-propionylamino]-(3,5-dimethoxy-phenyl)-acetic acid methyl ester 

Downstream Products

• 173383-20-5 C₄₈H₄₇Cl₂IN₄O₁₂ 
• 173383-21-6 (S)-{[(8R,11R,14S)-8-Amino-11-(4-benzyloxy-phenyl)-18,19-dichloro-4-hydroxy-5-iodo-9,12-dioxo-2-oxa-10,13-diaza-tricyclo[14.2.2.1^3,7]henicosa-1⁽¹⁹⁾,3⁽²¹⁾,4,6,16⁽²⁰⁾,17-hexaene-14-carbonyl]-amino}-(3,5-dimethoxy-phenyl)-acetic acid methyl ester 
• 173383-24-9 C₆₇H₇₁Cl₄IN₈O₁₇ 
• 173383-25-0 C₆₇H₇₀Cl₄N₈O₁₇ 
• 173383-19-2 (S)-[(S)-2-{(R)-2-(4-Benzyloxy-phenyl)-2-[(R)-2-tert-butoxycarbonylamino-2-(4-hydroxy-3,5-diiodo-phenyl)-acetylamino]-acetylamino}-3-(3,5-dichloro-4-hydroxy-phenyl)-propionylamino]-(3,5-dimethoxy-phenyl)-acetic acid methyl ester 

Relevant academic research and scientific papers

Synthetic Studies on Vancomycin: Synthesis of Seco-Aglucovancomycins

Preparation of the vancomycin analogs (SAV-1 and SAV-2) is described.The key step is construction of a bicyclic diaryl ether residue by means of thallium(III) oxidation of the corresponding halogenated phenols.