Medium-ring aminocyclitols: a concise synthesis of nine-membered aminocarbasugar analogs and the solid-state supramolecular architectures of two key precursors

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• 作者：Goverdhan Mehta^a ; ^b ; ^{gmsc@uohyd.ernet.in"" rel=""nofollow} ; ^{gm@orgchem.iisc.ernet.in"" rel=""nofollow} ; Raja Mohanrao^a ; Sreenivas Katukojvala^a ; Yannick Landais^c ; Saikat Sen^b
• 关键词：Aminocyclitols ; Carbasugars ; Baeyer– ; Villiger oxidation ; Dihydroxylation ; Hydrogen bonding
• 刊名：Tetrahedron Letters
• 出版年：2011
• 出版时间：1 June 2011
• 年：2011
• 卷：52
• 期：22
• 页码：2893-2897
• 全文大小：1083 K

文摘

A stereocontrolled synthesis of nine-membered aminocarbasugar analogs (amino-cyclononanoses) from a rigid bicyclo[4.3.1]deca-2,4-dien-10-one platform, harboring a latent functionalized cyclononane ring, is described.