Gray L, Schreiber SL. Skeletal diversity in small-molecule synthesis using ligand-controlled catalysis. J Comb Chem. 2007;9(6):1028-35. doi:10.1021/cc7001028
Looper RE, Pizzirani D, Schreiber SL. Macrocycloadditions leading to conformationally restricted small molecules. Org Lett. 2006;8(10):2063-6. doi:10.1021/ol0604724
Kumagai N, Muncipinto G, Schreiber SL. Short synthesis of skeletally and stereochemically diverse small molecules by coupling petasis condensation reactions to cyclization reactions. Angew Chem Int Ed Engl. 2006;45(22):3635-8. doi:10.1002/anie.200600497
Kumar N, Kiuchi M, Tallarico JA, Schreiber SL. Small-molecule diversity using a skeletal transformation strategy. Org Lett. 2005;7(13):2535-8. doi:10.1021/ol0504345
Oguri H, Schreiber SL. Skeletal diversity via a folding pathway: synthesis of indole alkaloid-like skeletons. Org Lett. 2005;7(1):47-50. doi:10.1021/ol047945w
Krishnan S, Schreiber SL. Syntheses of stereochemically diverse nine-membered ring-containing biaryls. Org Lett. 2004;6(22):4021-4. doi:10.1021/ol048273c
Schmidt DR, Kwon O, Schreiber SL. Macrolactones in diversity-oriented synthesis: preparation of a pilot library and exploration of factors controlling macrocyclization. J Comb Chem. 2004;6(2):286-92. doi:10.1021/cc020076m
Sello JK, Andreana PR, Lee D, Schreiber SL. Stereochemical control of skeletal diversity. Org Lett. 2003;5(22):4125-7. doi:10.1021/ol035773h
Burke MD, Berger EM, Schreiber SL. Generating diverse skeletons of small molecules combinatorially. Science. 2003;302(5645):613-8. doi:10.1126/science.1089946
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