Diversity-oriented synthesis and solid-phase organic synthesis under controlled microwave heating

被引:29
作者
Dai, Wei-Min [1 ,2 ]
Shi, Jianyu [1 ,3 ]
机构
[1] Zhejiang Univ, Dept Chem, Lab Asymmetr Catalysis & Synthesis, Hangzhou 310027, Peoples R China
[2] Hong Kong Univ Sci & Technol, Canc Res Ctr, Hong Kong, Hong Kong, Peoples R China
[3] Hong Kong Univ Sci & Technol, Dept Chem, Hong Kong, Hong Kong, Peoples R China
关键词
annulation; diversity-oriented synthesis; heterocycles; linker; microwave; multi-component reactions; solid-phase organic synthesis; tandem reactions;
D O I
10.2174/138620707783220338
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Diversity-oriented organic synthesis (DOS) and solid-phase organic synthesis (SPOS) are proven technologies for generating small molecule libraries for chemical genetics studies. Integration of controlled microwave heating with DOS and SPOS not only speeds up the library preparation process but also offers unique opportunities in tackling issues which are hardly addressed by thermal heating. Microwave-assisted synthesis is illustrated for (a) highly regioselective Wittig olefination of cycloalkanones by accurate regulation of temperature; (b) tandem Wittig-IMDA sequence toward stereochemical diversity of gamma-butyrolactones; (c) one-pot alkylation-amidation approach toward appendage diversity through use of building blocks; and (d) one-pot U-4CR-annulation strategy toward skeletal diversity via careful reaction design. Microwave-assisted solid-phase organic synthesis (MASPOS) is highlighted by incorporating with split-pool combinatorial synthesis (SPCS) of indole sulfonamides via a key on-resin Cu(II)- or Pd(II)-catalyzed heteroannulation under microwave heating. Design and fabrication of a novel diglycine-derived cat center dot linker are described and its role in facilitating on-resin reaction is evaluated. A traceless synthesis of indole sulfonamides via microwave-assisted Cu(II)-catalyzed heteroannulation of the cat center dot linker-tethered substrates is also given.
引用
收藏
页码:837 / 856
页数:20
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