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
Looper RE, Pizzirani D, Schreiber SL. Macrocycloadditions leading to conformationally restricted small molecules. Org Lett. 2006;8(10):2063-6. doi:10.1021/ol0604724
Franz AK, Dreyfuss PD, Schreiber SL. Synthesis and cellular profiling of diverse organosilicon small molecules. J Am Chem Soc. 2007;129(5):1020-1. doi:10.1021/ja067552n
Wang Y, Jimenez M, Sheehan P, et al. Selective access to trisubstituted macrocyclic E- and Z-alkenes from the ring-closing metathesis of vinylsiloxanes. Org Lett. 2013;15(6):1218-21. doi:10.1021/ol400134d
Rahaim RJ, Shaw JT. Zinc-catalyzed silylation of terminal alkynes. J Org Chem. 2008;73(7):2912-5. doi:10.1021/jo702557d
Gerard B, O’Shea MW, Donckele E, et al. Application of a catalytic asymmetric Povarov reaction using chiral ureas to the synthesis of a tetrahydroquinoline library. ACS Comb Sci. 2012;14(11):621-30. doi:10.1021/co300098v
Lowe JT, Lee MD, Akella LB, et al. Synthesis and profiling of a diverse collection of azetidine-based scaffolds for the development of CNS-focused lead-like libraries. J Org Chem. 2012;77(17):7187-211. doi:10.1021/jo300974j
Fitzgerald ME, Mulrooney CA, Duvall JR, et al. Build/couple/pair strategy for the synthesis of stereochemically diverse macrolactams via head-to-tail cyclization. ACS Comb Sci. 2012;14(2):89-96. doi:10.1021/co200161z
Urgaonkar S, La Pierre HS, Meir I, Lund H, Raychaudhuri D, Shaw JT. Synthesis of antimicrobial natural products targeting FtsZ: (+/-)-dichamanetin and (+/-)-2’ ’’-hydroxy-5’ ’-benzylisouvarinol-B. Org Lett. 2005;7(25):5609-12. doi:10.1021/ol052269z
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