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Structure-based design and synthesis of pyrazinones containing novel P1 'side pocket' moieties as inhibitors of TF/VIIa.
Bioorg Med Chem Lett. 2005 Jun 15;15(12):3006-11. doi: 10.1016/j.bmcl.2005.04.037.
Bioorg Med Chem Lett. 2005.
PMID: 15913999
Design, synthesis, and biological evaluation of pyrazinones containing novel P1 needles as inhibitors of TF/VIIa.
Trujillo JI, Huang HC, Neumann WL, Mahoney MW, Long S, Huang W, Garland DJ, Kusturin C, Abbas Z, South MS, Reitz DB.
Trujillo JI, et al.
Bioorg Med Chem Lett. 2007 Aug 15;17(16):4568-74. doi: 10.1016/j.bmcl.2007.05.090. Epub 2007 Jun 6.
Bioorg Med Chem Lett. 2007.
PMID: 17566736
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Switchable catalysis: modular synthesis of functionalized Pyrimidinones via selective sulfide and halide cross-coupling chemistry.
Kusturin C, Liebeskind LS, Rahman H, Sample K, Schweitzer B, Srogl J, Neumann WL.
Kusturin C, et al.
Org Lett. 2003 Nov 13;5(23):4349-52. doi: 10.1021/ol035649y.
Org Lett. 2003.
PMID: 14601997
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A new catalytic cross-coupling approach for the synthesis of protected aryl and heteroaryl amidines.
Kusturin CL, Liebeskind LS, Neumann WL.
Kusturin CL, et al.
Org Lett. 2002 Mar 21;4(6):983-5. doi: 10.1021/ol025547s.
Org Lett. 2002.
PMID: 11893202
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