Williams DR, Mondal PK, Bawel SA, Nag PP. Stereocontrolled synthesis of the tricyclic ABC ring system of daphnicyclidin A. Org Lett. 2014;16(7):1956-9. doi:10.1021/ol5005092
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
Sello JK, Andreana PR, Lee D, Schreiber SL. Stereochemical control of skeletal diversity. Org Lett. 2003;5(22):4125-7. doi:10.1021/ol035773h
Micalizio GC, Schreiber SL. A boronic ester annulation strategy for diversity-oriented organic synthesis. Angew Chem Int Ed Engl. 2002;41(1):152-4.
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