[2]-Ladderanes as isosteres for meta-substituted aromatic rings and rigidified cyclohexanes
The development of new classes of isosteres and building blocks is crucial to the advancement of medicinal chemistry programs. Here, the authors report the synthesis and development of ladderanes to act as replacements for meta-substituted aromatic rings and cyclohexanes.
Main Authors: | Rachel C. Epplin, Shashwati Paul, Loïc Herter, Christophe Salome, Erin N. Hancock, Jay F. Larrow, Erich W. Baum, David R. Dunstan, Carol Ginsburg-Moraff, Thomas C. Fessard, M. Kevin Brown |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2022-10-01
|
Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-022-33827-3 |
Similar Items
-
Occurrence and distribution of ladderane oxidation products in different oceanic regimes
by: D. Rush, et al.
Published: (2012-07-01) -
Rigidified malononitrile- and ketone-merocyanines in rigid environments
by: Tomce Runcevski, et al.
Published: (2015-05-01) -
Investigation of Proposed Ladderane Biosynthetic Genes from Anammox Bacteria by Heterologous Expression in E. coli.
by: Pouya Javidpour, et al.
Published: (2016-01-01) -
Novel African trypanocidal agents: membrane rigidifying peptides.
by: John M Harrington, et al.
Published: (2012-01-01) -
A comparative genomics study of genetic products potentially encoding ladderane lipid biosynthesis
by: Jetten Mike SM, et al.
Published: (2009-02-01)