Synthesis of 16-membered ring macrolide antibiotics I. Stereoselective construction of the ‘right wing” of the carbomycins and leucomycins from <span class="math"><math><mtext>D</mtext></math></span>-glucose期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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Synthesis of 16-membered ring macrolide antibiotics I. Stereoselective construction of the ‘right wing” of the carbomycins and leucomycins from $D$ -glucose

Authors:	KC Nicolaou MR Pavia SP Seitz

Institution:	Department of Chemistry, University of Pennsylvania Philadelphia, PA 19104 U.S.A.

Abstract:	$D$ -Glucose was converted to a backbone chain containing the appropriate functionalities and correct stereochemistry for the construction of the C1–C9 fragment of the 16-membered ring macrolide antibiotics carbomycin A and B and leucomycin A₃.

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