Ontology highlight
ABSTRACT:
SUBMITTER: Gianatassio R
PROVIDER: S-EPMC4730898 | biostudies-literature | 2016 Jan
REPOSITORIES: biostudies-literature
Gianatassio Ryan R Lopchuk Justin M JM Wang Jie J Pan Chung-Mao CM Malins Lara R LR Prieto Liher L Brandt Thomas A TA Collins Michael R MR Gallego Gary M GM Sach Neal W NW Spangler Jillian E JE Zhu Huichin H Zhu Jinjiang J Baran Phil S PS
Science (New York, N.Y.) 20160101 6270
To optimize drug candidates, modern medicinal chemists are increasingly turning to an unconventional structural motif: small, strained ring systems. However, the difficulty of introducing substituents such as bicyclo[1.1.1]pentanes, azetidines, or cyclobutanes often outweighs the challenge of synthesizing the parent scaffold itself. Thus, there is an urgent need for general methods to rapidly and directly append such groups onto core scaffolds. Here we report a general strategy to harness the em ...[more]