Rhodium-Catalyzed Conversion of Furans to Highly Functionalized Pyrroles von Parr, Brendan T, Green, Samantha A, Davies, Huw M. L

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A concise synthesis of (+)-batzelladine B from simple pyrrole-based starting materials von Parr, Brendan T., Economou, Christos, Herzon, Seth B.

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Highly Stereoselective C–C Bond Formation by Rhodium-Catalyzed Tandem Ylide Formation/[2,3]-Sigmatropic Rearrangement between Donor/Acceptor Carbenoids and Chiral Allylic Alcohols... von Li, Zhanjie, Parr, Brendan T., Davies, Huw M. L.

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Highly stereoselective synthesis of cyclopentanes bearing four stereocentres by a rhodium carbene-initiated domino sequence von Parr, Brendan T, Davies, Huw M.L.

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Rhodium(II)-Catalyzed Cross-Coupling of Diazo Compounds von Hansen, Jørn H, Parr, Brendan T, Pelphrey, Philip, Jin, Quihui, Autschbach, Jochen, Davies, Huw M.L

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Asymmetric Synthesis of Highly Functionalized Cyclopentanes by a Rhodium- and Scandium-Catalyzed Five-Step Domino Sequence von Parr, Brendan T, Li, Zhanjie, Davies, Huw M L

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Implementation of the CYP Index for the Design of Selective Tryptophan-2,3-dioxygenase Inhibitors von Parr, Brendan T, Pastor, Richard, Sellers, Benjamin D, Pei, Zhonghua, Jaipuri, Firoz A, Castanedo, Georgette M, Gazzard, Lewis, Kumar, Sanjeev, Li, Xiaokai, Liu, Wen, Mendonca, Rohan, Pavana, Roheeth K, Potturi, Hima, Shao, Cheng, Velvadapu, Venkata, Waldo, Jesse P, Wu, Guosheng, Yuen, Po-wai, Zhang, Zuhui, Zhang, Yamin, Harris, Seth F, Oh, Angela J, DiPasquale, Antonio, Dement, Kevin, La, Hank, Goon, Leanne, Gustafson, Amy, VanderPorten, Erica C, Mautino, Mario R, Liu, Yichin

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Rhodium-Catalyzed Tandem Cyclopropanation/Cope Rearrangement of 4-Alkenyl-1-sulfonyl-1,2,3-triazoles with Dienes von Parr, Brendan T., Davies, Huw M. L.

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Enyne Amides to Fused Pyridones: Scope and Limitations von Labadie, Sharada S., Thai, Karine, Grandner, Jessica M., Liu, Yanzhou, Parr, Brendan T.

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A convergent approach to batzelladine alkaloids. Total syntheses of (+)-batzelladine E, (−)-dehydrobatzelladine C, and (+)-batzelladine K von Economou, Christos, Romaire, Justin P., Scott, Tony Z., Parr, Brendan T., Herzon, Seth B.

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Discovery of a Novel Mutant-Selective Epidermal Growth Factor Receptor Inhibitor Using an In Silico Enabled Drug Discovery Platform von Igawa, Hideyuki, Konst, Zef A., Therrien, Eric, Shelley, Mee, Koldsø, Heidi, Bos, Pieter H., Negri, Ana, Verras, Andreas, Guo, Jiaye, Dahlgren, Markus K., Levinson, Adam, Parr, Brendan T., Kurhade, Suresh E., Latthe, Prashant, Shetty, Rajesha, Santhanakrishnan, Sridhar, Amberg-Johnson, Katherine, Futran, Alan S., Atsriku, Christian, Pelletier, Robert D., Liu, Zhijian, Bell, Jeffrey A., Bhat, Sathesh, Svensson, Mats, Gerasyuto, Aleksey I.

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Unearthing the Subtleties of Rhodium(II)-Catalyzed Carbenoid Cycloadditions to Furans with an N‑Sulfonyl-1,2,3-triazole Probe von Bettencourt, Christian J., Krainz, Tanja, Chow, Sharon, Parr, Brendan T., Tracy, William F., Bernhardt, Paul V., Davies, Huw M. L., Williams, Craig M.

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Targeting KRAS Mutant Cancers via Combination Treatment: Discovery of a 5‑Fluoro-4-(3H)‑quinazolinone Aryl Urea pan-RAF Kinase Inhibitor von Huestis, Malcolm P, Dela Cruz, Darlene, DiPasquale, Antonio G, Durk, Matthew R, Eigenbrot, Charles, Gibbons, Paul, Gobbi, Alberto, Hunsaker, Thomas L, La, Hank, Leung, Dennis H, Liu, Wendy, Malek, Shiva, Merchant, Mark, Moffat, John G, Muli, Christine S, Orr, Christine J, Parr, Brendan T, Shanahan, Frances, Sneeringer, Christopher J, Wang, Weiru, Yen, Ivana, Yin, Jianping, Siu, Michael, Rudolph, Joachim

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Stereoselective Synthesis of Highly Substituted Cyclohexanes by a Rhodium-Carbene Initiated Domino Sequence von Parr, Brendan T, Davies, Huw M. L

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Discovery of Selective Tertiary Amide Inhibitors of Cyclin-Dependent Kinase 2 (CDK2) von Zeng, Mingshuo, Grandner, Jessica M., Bryan, Marian C., Verma, Vishal, Larouche-Gauthier, Robin, Leclerc, Jean-Philippe, Zhao, Liang, Haghshenas, Pouyan, Aubert-Nicol, Samuel, Yadav, Arun, Ashley, Melissa, Chen, Jacob Z., Durk, Matthew, Samy, Karen E., Nespi, Marika, Levy, Elizabeth, Merrick, Karl, Moffat, John G., Murray, Jeremy, Oh, Angela, Orr, Christine, Segal, Ehud, Sims, Jessica, Sneeringer, Christopher, Prangley, Madeleine, Vartanian, Steffan, Magnuson, Steven, Parr, Brendan T.

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Targeting KRAS Mutant Cancers via Combination Treatment: Discovery of a Pyridopyridazinone pan-RAF Kinase Inhibitor von Huestis, Malcolm P, Durk, Matthew R, Eigenbrot, Charles, Gibbons, Paul, Hunsaker, Thomas L, La, Hank, Leung, Dennis H, Liu, Wendy, Malek, Shiva, Merchant, Mark, Moffat, John G, Muli, Christine S, Orr, Christine J, Parr, Brendan T, Shanahan, Frances, Sneeringer, Christopher J, Wang, Weiru, Yen, Ivana, Yin, Jianping, Rudolph, Joachim, Siu, Michael

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Michael−Aldol Ring Closures with Dihapto-Coordinated Pyrrole Complexes and the Synthesis of Tetrahydroindole Cores von Welch, Kevin D, Harrison, Daniel P, Sabat, Michal, Hejazi, Emily Z, Parr, Brendan T, Fanelli, Matthew G, Gianfrancesco, Nicole A, Nagra, Dalsher S, Myers, William H, Harman, W. Dean

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ChemInform Abstract: Stereoselective Synthesis of Highly Substituted Cyclohexanes by a Rhodium-Carbene Initiated Domino Sequence von Parr, Brendan T., Davies, Huw M. L.

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Asymmetric synthesis of highly functionalized cyclopentanes by a rhodium- and scandium-catalyzed five-step domino sequenceElectronic supplementary information (ESI) available: Full... von Parr, Brendan T, Li, Zhanjie, Davies, Huw M. L

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ChemInform Abstract: Rhodium Carbenes von Davies, Huw M. L., Parr, Brendan T.

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