Applications of multicomponent reactions to the synthesis of diverse heterocyclic scaffolds.

Applications of multicomponent reactions to the synthesis of diverse heterocyclic scaffolds.
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DOI:
10.1002/chem.200802140
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发表时间:
2009
影响因子:
4.3
通讯作者:
Martin, Stephen E.
Martin, Stephen E.
中科院分区:
化学2区
文献类型:
--
作者:
Sunderhaus, James D.;Martin, Stephen E.

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多组分反应(MCRs)及其后续环化反应的排序是快速合成各种杂环支架的有力手段。最佳的MCR具有足够的灵活性,可以用来生成带有各种官能团的加合物,然后可以选择性地配对以实现不同的环化歧管,从而导致不同的产品集合。随着人们对多样性导向合成的兴趣日益浓厚,这一文库合成范式得到了越来越多的关注,这激发了用于构建多种杂环支架的mcr的设计和实现方面的许多进展。
The sequencing of multicomponent reactions (MCRs) and subsequent cyclization reactions is a powerful stratagem for the rapid synthesis of diverse heterocyclic scaffolds. The optimal MCR is sufficiently flexible that it can be employed to generate adducts bearing a variety of functional groups that may then be selectively paired to enable different cyclization manifolds, thereby leading to a diverse collection of products. The growing interest in diversity-oriented synthesis has led to increased attention to this paradigm for library synthesis, which has inspired many advances in the design and implementation of MCRs for the construction of diverse heterocyclic scaffolds.
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