Construction of Polyheterocyclic Benzopyran Library with Diverse Core Skeletons through Diversity-Oriented Synthesis Pathway: Part II

被引:23
作者
Zhu, Mingyan [1 ]
Lim, Byung Joon [1 ]
Koh, Minseob [1 ]
Park, Seung Bum [1 ,2 ]
机构
[1] Seoul Natl Univ, Dept Chem, Seoul 151747, South Korea
[2] Seoul Natl Univ, Dept Biophys & Chem Biol, Seoul 151747, South Korea
基金
新加坡国家研究基金会;
关键词
benzopyran; parallel synthesis; fluorous tag; diversity-oriented synthesis; skeletal diversity; AZIDE-ALKYNE CYCLOADDITION; PRIVILEGED STRUCTURES; COMBINATORIAL LIBRARIES; ORGANIC-SYNTHESIS; SOLID-PHASE; CHEMISTRY; DISCOVERY; INHIBITORS; ACTIVATOR; ANALOGS;
D O I
10.1021/co2001907
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
As a continuation of our previous report (J. Comb. Chem. 2010, 12, 548-558), we accomplished the diversity-oriented synthesis of polyheterocyclic small-molecule library with privileged benzopyran substructure. To ensure the synthetic efficiency, we utilized the solid phase parallel platform and the fluorous-tag-based solution-phase parallel platform to construct a 284-member polyheterocyclic library with six distinct, core skeletons with an average purity of 87% on a scale of 5-10 mg. This library was designed to maximize the skeletal diversity with discrete core skeletons in three-dimensional space and the combinatorial diversity with four different benzopyranyl starting materials and various building blocks. Together with our reported benzopyranyl library, we completed the construction of polyhetererocyclic benzopyran library with 11unique scaffolds and their molecular diversity was visualized in chemical space using principle component analysis (PCA).
引用
收藏
页码:124 / 134
页数:11
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