| Literature DB >> 34244445 |
Jin-Xin Zhao1,2, Yu-Xuan Chang1, Chi He1, Benjamin J Burke3, Michael R Collins4, Matthew Del Bel3, Jeff Elleraas3, Gary M Gallego3, T Patrick Montgomery3, James J Mousseau5, Sajiv K Nair3, Matthew A Perry5, Jillian E Spangler3, Julien C Vantourout1, Phil S Baran6.
Abstract
The development of a versatile platform for the synthesis of 1,2-difunctionalized bicyclo[1.1.1]pentanes to potentially mimic ortho/meta-substituted arenes is described. The syntheses of useful building blocks bearing alcohol, amine, and carboxylic acid functional handles have been achieved from a simple common intermediate. Several ortho- and meta-substituted benzene analogs, as well as simple molecular matched pairs, have also been prepared using this platform. The results of in-depth ADME (absorption, distribution, metabolism, and excretion) investigations of these systems are presented, as well as computational studies which validate the ortho- or meta-character of these bioisosteres.Entities:
Keywords: bioisosteres; medicinal chemistry; synthesis
Mesh:
Substances:
Year: 2021 PMID: 34244445 PMCID: PMC8285974 DOI: 10.1073/pnas.2108881118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205