Rees MG, Seashore-Ludlow B, Cheah JH, et al. Correlating chemical sensitivity and basal gene expression reveals mechanism of action. Nat Chem Biol. 2016;12(2):109-16. doi:10.1038/nchembio.1986
Heemstra JM, Liu DR. Templated synthesis of peptide nucleic acids via sequence-selective base-filling reactions. J Am Chem Soc. 2009;131(32):11347-9. doi:10.1021/ja904712t
Muncipinto G, Kaya T, Wilson A, Kumagai N, Clemons PA, Schreiber SL. Expanding stereochemical and skeletal diversity using petasis reactions and 1,3-dipolar cycloadditions. Org Lett. 2010;12(22):5230-3. doi:10.1021/ol102266j
Ng PY, Masse CE, Shaw JT. Cycloaddition reactions of imines with 3-thiosuccinic anhydrides: synthesis of the tricyclic core of martinellic acid. Org Lett. 2006;8(18):3999-4002. doi:10.1021/ol061473z
Shaw AT, Friboulet L, Leshchiner I, et al. Resensitization to Crizotinib by the Lorlatinib ALK Resistance Mutation L1198F. N Engl J Med. 2016;374(1):54-61. doi:10.1056/NEJMoa1508887
Tse BN, Snyder TM, Shen Y, Liu DR. Translation of DNA into a library of 13,000 synthetic small-molecule macrocycles suitable for in vitro selection. J Am Chem Soc. 2008;130(46):15611-26. doi:10.1021/ja805649f
Pizzirani D, Kaya T, Clemons PA, Schreiber SL. Stereochemical and skeletal diversity arising from amino propargylic alcohols. Org Lett. 2010;12(12):2822-5. doi:10.1021/ol100914b
Masse CE, Ng PY, Fukase Y, Sanchez-Roselló M, Shaw JT. Divergent structural complexity from a linear reaction sequence: synthesis of fused and spirobicyclic gamma-lactams from common synthetic precursors. J Comb Chem. 2006;8(3):293-6. doi:10.1021/cc050153o
Tibbitt MW, Dahlman JE, Langer R. Emerging Frontiers in Drug Delivery. J Am Chem Soc. 2016;138(3):704-17. doi:10.1021/jacs.5b09974
Rozenman MM, Kanan MW, Liu DR. Development and initial application of a hybridization-independent, DNA-encoded reaction discovery system compatible with organic solvents. J Am Chem Soc. 2007;129(48):14933-8. doi:10.1021/ja074155j