352032-78-1Relevant articles and documents
Synthesis, stereochemical assignment and biological activity of a novel series of C-4″ modified aza-macrolides
Bronk, Brian S.,Letavic, Michael A.,Bertsche, Camilla D.,George, David M.,Hayashi, Shigeru F.,Kamicker, Barbara J.,Kolosko, Nicole L.,Norcia, Laura J.,Rushing, Margaret A.,Santoro, Sheryl L.,Yang, Bingwei V.
, p. 1955 - 1958 (2003)
Modification of the cladinose C-4″ position via manipulation of the corresponding keto derivatives afforded two stereochemically pure series of compounds. The synthesis and structure determination of these compounds is described within. The in vitro and i
Method for preparing 2-iodoxybenzoic acid
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Paragraph 0038-0050, (2019/02/13)
The invention relates to a method for preparing 2-iodoxybenzoic acid, and belongs to the technical field of synthesis of rings containing a halogen atom as a heterocyclic atom. The method comprises the following steps: adding an oxidant to 2-iodobenzoic acid used as a raw material, carrying out a reaction in an acidic solution at 50-120 DEG C for 1-6 h, and purifying the obtained reaction productto obtain the 2-iodoxybenzoic acid. The method has the advantages of small toxicity, mild technologic conditions, economical and cheap property and suitableness for industrialization when applied to the synthesis of a catalyst.
Tulathromycin oxalate
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Paragraph 0059; 0060, (2017/12/27)
The invention discloses salt of tulathromycin, particularly oxalate, a preparation method of tulathromycin oxalate and application of tulathromycin oxalate to preparation of tulathromycin.