From Polymer to Small Organic Molecules: A Tight Relationship between Radical Chemistry and Solid-Phase Organic Synthesis

被引:10
作者
Mirizzi, Danilo [1 ]
Pulici, Maurizio [1 ]
机构
[1] Nerviano Med Sci SRL, Dept Chem Core Technol, I-20014 Nerviano, MI, Italy
来源
MOLECULES | 2011年 / 16卷 / 04期
关键词
radical; solid-phase; SPS; polymer-assisted synthesis; polymer-supported reagents; CROSS-LINKED POLYSTYRENE; CARBON-CARBON BOND; BARTON-MCCOMBIE DEOXYGENATION; ADDITION-CYCLIZATION REACTION; SUPPORTED ORGANOTIN HYDRIDES; OXIME ETHERS; STEREOCONTROLLED SYNTHESIS; 1,2-SELENO MIGRATIONS; MEDIATED CYCLIZATIONS; SAMARIUM(II) IODIDE;
D O I
10.3390/molecules16043252
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Since Gomberg's discovery of radicals as chemical entities, the interest around them has increased through the years. Nowadays, radical chemistry is used in the synthesis of 75% of all polymers, inevitably establishing a close relationship with Solid-Phase Organic Synthesis. More recently, the interest of organic chemists has shifted towards the application of usual "in-solution" radical chemistry to the solid-phase, ranging from the use of supported reagents for radical reactions, to the development of methodologies for the synthesis of small molecules or potential libraries. The aim of this review is to put in perspective radical chemistry, moving it away from its origin as a synthetic means for solid supports, to becoming a useful tool for the synthesis of small molecules.
引用
收藏
页码:3252 / 3314
页数:63
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