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Erythromycin study: 9-Amino-3-0-cladinosyl-5-0-desosaminyl-6,11,12- tryhydroxy-2,4,6,8,10,12-hexamethylpentadecane-13-olide

✍ Scribed by Slobodan Djokić; Zrinka Tamburašev

Publisher
Elsevier Science
Year
1967
Tongue
French
Weight
149 KB
Volume
8
Category
Article
ISSN
0040-4039

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✦ Synopsis

IN reduction of nyl in position Yugoslavia (Received 23 January 1967) erythromycin (I) to dihydrberythromycin (VI) the keto carbo-9 of the aglycon part of the molecule was transformed into a hyaroxyl group.lp2 No other reactions involving specific changes in keto grcup of I are described. Attempts to prepare the usual carbonyl derivatives of

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