Use of a Tandem Prins/Friedel–Crafts Reaction in the Construction of the Indeno-Tetrahydropyridine Core of the Haouamine Alkaloids: Formal Synthesis of (−)-Haouamine A von Fenster, Erik, Fehl, Charlie, Aubé, Jeffrey

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A Synthetic Approach to the Fusicoccane A−B Ring Fragment Based on a Pauson−Khand Cycloaddition/Norrish Type 1 Fragmentation von Dake, Gregory R, Fenster, Erik E, Patrick, Brian O

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Automated three-component synthesis of a library of γ-lactams von Fenster, Erik, Hill, David, Reiser, Oliver, Aubé, Jeffrey

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A Convenient Method for the Conversion of Hindered Carboxylic Acids to N-Methoxy-N-methyl (Weinreb) Amides von Woo, Jacqueline C. S, Fenster, Erik, Dake, Gregory R

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Nucleophilic Addition to Iminium Ethers in the Preparation of Functionalized N-Alkyl Heterocycles von Fenster, Erik, Smith, Brenton T, Gracias, Vijaya, Milligan, Gregory L, Aubé, Jeffrey

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Palladium-catalyzed substitution of (coumarinyl)methyl acetates with C-, N-, and S-nucleophiles von Chattopadhyay, Kalicharan, Fenster, Erik, Grenning, Alexander J, Tunge, Jon A

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Automated Synthesis of a 184-Member Library of Thiadiazepan-1,1-dioxide-4-ones von Fenster, Erik, Long, Toby R, Zang, Qin, Hill, David, Neuenswander, Benjamin, Lushington, Gerald H, Zhou, Aihua, Santini, Conrad, Hanson, Paul R

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Neprilysin inhibitors von Gendron, Roland, Fenster, Erik, Fleury, Melissa, Hughes, Adam D, Moran, Edmund J

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(2R,4R)-5-(5'-CHLORO-2'-FLUOROBIPHENYL-4-YL)-2-HYDROXY-4-[(5-METHYLOXAZOLE-2-CARBONYL)AMINO]PENTANOIC ACID von BEAUSOLEIL, ANNE-MARIE, FLEURY, MELISSA, FENSTER, ERIK, THALLADI, VENKAT R, RAPTA, MIROSLAV, HUGHES, ADAM D

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NEPRILYSIN INHIBITORS von Gendron, Roland, Fenster, Erik, Fleury, Melissa, Hughes, Adam D, Moran, Edmund J

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(2R,4R)-5-(5′-chloro-2′-fluorobiphenyl-4-yl)-2-hydroxy-4-[(5-methyloxazole-2-carbonyl)amino]pentanoic acid von Rapta, Miroslav, Fenster, Erik, Thalladi, Venkat R, Fleury, Melissa, Hughes, Adam D, Beausoleil, Anne-Marie

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Neprilysin inhibitors von Gendron, Roland, Fenster, Erik, Fleury, Melissa, Hughes, Adam D, Moran, Edmund J

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SUBSTITUTED PYRIDINES AND METHODS OF USE von Sullivan, Steven D.E, Kozak, Jennifer, Zhao, Chen, Owens, Christina, Fenster, Erik, Loo, Mandy, Kulyk, Svitlana, Allegretti, Paul, Hughes, Adam D

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Fused pyrimidine pyridinone compounds as JAK inhibitors von Palermo, Anthony Francesco, Wang, Diana Jin, Lam, Tom M, McKinnell, Robert Murray, Fenster, Erik, Boralsky, Luke, Fraga, Breena

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(2R,4R)-5-(5'-CHLORO-2'-FLUOROBIPHENYL-4-YL)-2-HYDROXY-4-[(5-METHYLOXAZOLE-2-CARBONYL)AMINO]PENTANOIC ACID von BEAUSOLEIL, Anne-Marie, RAPTA, Miroslav, HUGHES, Adam D, FENSTER, Erik, FLEURY, Melissa, THALLADI, Venkat R

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Imidazole and triazole containing bicyclic compounds as JAK inhibitors von Palermo, Anthony Francesco, Lam, Tom M, McKinnell, Robert Murray, Fenster, Erik

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Substituted pyridines and methods of use von Kozak, Jennifer, Owens, Christina, Sullivan, Steven D. E, Fenster, Erik, Loo, Mandy, Kulyk, Svitlana, Allegretti, Paul, Hughes, Adam D

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PYRAZOLO AND TRIAZOLO BICYCLIC COMPOUNDS AS JAK KINASE INHIBITORS von WANG, Diana Jin, LOO, Mandy, RAPTA, Miroslav, LAM, Tom M, PALERMO, Anthony Francesco, FENSTER, Erik, MCKINNELL, Robert Murray, NZEREM, Jerry, DABROS, Marta, THALLADI, Venkat R, FRAGA, Breena

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Neprilysin inhibitors von Fenster, Erik, Fleury, Melissa, Hughes, Adam D

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NEPRILYSIN INHIBITORS von Fenster, Erik, Fleury, Melissa, Hughes, Adam D

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