Andreana PR, Liu CC, Schreiber SL. Stereochemical control of the Passerini reaction. Org Lett. 2004;6(23):4231-3. doi:10.1021/ol0482893
Sello JK, Andreana PR, Lee D, Schreiber SL. Stereochemical control of skeletal diversity. Org Lett. 2003;5(22):4125-7. doi:10.1021/ol035773h
Chen C, Li X, Schreiber SL. Catalytic asymmetric [3+2] cycloaddition of azomethine ylides. Development of a versatile stepwise, three-component reaction for diversity-oriented synthesis. J Am Chem Soc. 2003;125(34):10174-5. doi:10.1021/ja036558z
Zhong C, Wang Y, Hung AW, Schreiber SL, Young DW. Diastereoselective control of intramolecular aza-Michael reactions using achiral catalysts. Org Lett. 2011;13(20):5556-9. doi:10.1021/ol202276h
Muncipinto G, Moquist PN, Schreiber SL, Schaus SE. Catalytic diastereoselective petasis reactions. Angew Chem Int Ed Engl. 2011;50(35):8172-5. doi:10.1002/anie.201103271
Kanan MW, Rozenman MM, Sakurai K, Snyder TM, Liu DR. Reaction discovery enabled by DNA-templated synthesis and in vitro selection. Nature. 2004;431(7008):545-9. doi:10.1038/nature02920
Bittker JA, Phillips KJ, Liu DR. Recent advances in the in vitro evolution of nucleic acids. Curr Opin Chem Biol. 2002;6(3):367-74.
Kelly AR, Wei J, Kesavan S, et al. Accessing skeletal diversity using catalyst control: formation of n and n + 1 macrocyclic triazole rings. Org Lett. 2009;11(11):2257-60. doi:10.1021/ol900562u
Luo T, Dai M, Zheng SL, Schreiber SL. Syntheses of α-pyrones using gold-catalyzed coupling reactions. Org Lett. 2011;13(11):2834-6. doi:10.1021/ol200794w
Rahaim RJ, Shaw JT. Zinc-catalyzed silylation of terminal alkynes. J Org Chem. 2008;73(7):2912-5. doi:10.1021/jo702557d