Concise and diversity-oriented synthesis of novel scaffolds embedded with privileged benzopyran motif

SK Ko, HJ Jang, E Kim, SB Park

Index: Ko, Sung Kon; Jang, Hwan Jong; Kim, Eunha; Park, Seung Bum Chemical Communications, 2006 , # 28 p. 2962 - 2964

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Citation Number: 34

Abstract

A branching DOS strategy for an unbiased natural product-like library with embedded privileged benzopyran motif was established to provide complexity and diversity of resulting heterocycles with desired drug-likeness. The importance of skeletal diversity conducted on a privileged substructure was demonstrated through the biological evaluation of a small molecule library representing 22 unique core skeletons via in vitro cytotoxicity assay.