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Homoharringtonine

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The homoharringtonine is synthesized using &delta;-methyl-&delta;-caprolactone (1) and ethanol as starting materials via ring opening and elimination of ethyl 5-methyl-4-hexenoate (2), 2 has condensation reaction with diethyl oxalate to give diethyl 2-(3-methyl-2-butenyl) malonate (3), 3 has &beta;-decarboxylation reaction with aqueous dimethylsulfoxide in the presence of sodium chloride to generate 6-methyl-2-oxo-5-heptenoic acid ethyl ester (4); 4 is subject to alkaline hydrolysis, oxalylation and further acylation of cephalotaxine to obtain 6-methyl-2-Oxo-5-heptenoic acid cephalomannine ester (6) and then subjected to a Rafalmacky reaction to give methyl 2-hydroxy-2-(4-methyl-3-pentenyl) succinate Cephalotaxine ester (7), 7 is subject to mercury hydroxylation and mercury removal reaction to obtain the end product, homoharringtonine. The reaction scheme is as follows:<br /> <img id="ProductImg2" src="/NewsImg/2016-11-23/2016112322285830349.png" alt="a chemical reaction route map for the laboratory synthesis of homoharringtonine" /><br /> Figure 2 is a chemical reaction route map for the laboratory synthesis of homoharringtonine.
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  • Homoharringtonine
  • US $0.00-0.00/mg
  • CAS:26833-87-4
  • Min. Order: 20mg
  • Purity: 98% HPLC
  • Supply Ability: 100kg
  • 2024-12-20
  • Homoharringtonine
  • US $0.00 /Kg/Bag
  • CAS:26833-87-4
  • Min. Order: 1KG
  • Purity: 98%min
  • Supply Ability: 100kg
  • 2024-12-13

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