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首页> 外文期刊>Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry >Chiral alpha,omega-diaminoethers derived from D-mannitol and L-treitol as building blocks for the synthesis of macrocyclic compounds possessing 1,3-benzenedicarboxamide or 2,6-pyridinedicarboxamide subunits
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Chiral alpha,omega-diaminoethers derived from D-mannitol and L-treitol as building blocks for the synthesis of macrocyclic compounds possessing 1,3-benzenedicarboxamide or 2,6-pyridinedicarboxamide subunits

机译:衍生自D-甘露醇和L-海藻糖醇的手性α,ω-二氨基醚,作为合成具有1,3-苯二甲酰胺或2,6-吡啶二甲酰胺亚基的大环化合物的基础

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摘要

Three new chiral alpha,omega -diaminoethers, derivatives Of D-mannitol and L-treitol, possessing C-2 symmetry are prepared. The alpha,omega -diaminoethers were applied to the macrocyclization reaction under non-high-dilution conditions, which afforded chiral macrocyclic diamides possessing either 2,6-pyridinedicarboxamide or 1,3-benzenedicarboxamide moieties. (C) 2001 Elsevier Science Ltd. All rights reserved. [References: 32]
机译:制备了具有C-2对称性的三种新的手性α,ω-二氨基醚,D-甘露醇和L-苏糖醇的衍生物。将α,ω-二氨基醚在非高稀释条件下用于大环化反应,得到具有2,6-吡啶二甲酰胺或1,3-苯二甲酰胺部分的手性大环二酰胺。 (C)2001 Elsevier ScienceLtd。保留所有权利。 [参考:32]

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