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无保护基合成:发明的机遇

Protecting-group-free synthesis as an opportunity for invention.

机构信息

Department of Chemistry, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, California 92037, USA.

出版信息

Nat Chem. 2009 Jun;1(3):193-205. doi: 10.1038/nchem.216.

Abstract

The constant pressure to prepare compounds in a more efficient manner has placed the process by which traditional synthetic chemistry is conducted under scrutiny. Areas that have the potential to be improved must be highlighted and modified, so that we can approach the criterion of the 'ideal synthesis'. One area that offers this prospect is the minimization of the use of protecting groups in synthesis. A protection/deprotection event introduces at least two steps into a sequence, incurring costs from additional reagents and waste disposal, and generally leads to a reduced overall yield. Here we present relevant historical context and highlight recent (post-2004) total syntheses that have developed new chemistry in an effort to exclude protecting groups. The invention of chemoselective methodologies is crucial to the execution of 'protecting-group-free' synthesis, and recent advances in this area are also highlighted.

摘要

为了更有效地制备化合物,人们一直面临着压力,这使得传统合成化学所采用的方法受到了严格的审查。必须突出和改进那些有改进潜力的领域,以便我们能够达到“理想合成”的标准。有一个领域提供了这种可能性,那就是尽量减少合成中保护基团的使用。保护/脱保护反应至少会在序列中引入两个步骤,这会增加额外试剂和废物处理的成本,并且通常会导致总收率降低。在这里,我们提供了相关的历史背景,并强调了最近(2004 年后)的全合成,这些全合成开发了新的化学方法,努力排除保护基团。选择性化学方法的发明对“无保护基团”合成的执行至关重要,该领域的最新进展也得到了强调。

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