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通过多组分结晶途径选择性制备难以捉摸的替代单一组分多晶型固体形式。

Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes.

作者信息

Thomas Lynne H, Wales Craig, Wilson Chick C

机构信息

Department of Chemistry, University of Bath, Bath BA2 7AY, UK.

出版信息

Chem Commun (Camb). 2016 May 31;52(46):7372-5. doi: 10.1039/c6cc01027j.

Abstract

A transferable, simple, method for producing previously elusive and novel polymorphic forms of important active pharmaceutical ingredients (APIs; paracetamol (acetaminophen), piroxicam and piracetam) is demonstrated. Nitrogen heterocyclic co-molecules are employed to influence the self-assembly crystallisation process in a multi-component environment. Previously unknown solvates have also been synthesised by this method.

摘要

展示了一种可转移的、简单的方法,用于制备重要活性药物成分(API;对乙酰氨基酚、吡罗昔康和吡拉西坦)以前难以捉摸的新型多晶型物。氮杂环共分子用于在多组分环境中影响自组装结晶过程。通过该方法还合成了以前未知的溶剂化物。

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