Lewis Base Catalysis in Organic Synthesis von Denmark, Scott E, Beutner, Gregory L

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TCFH–NMI: Direct Access to N‑Acyl Imidazoliums for Challenging Amide Bond Formations von Beutner, Gregory L, Young, Ian S, Davies, Merrill L, Hickey, Matthew R, Park, Hyunsoo, Stevens, Jason M, Ye, Qingmei

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Lewis Base Catalysis of the Mukaiyama Directed Aldol Reaction: 40Years of Inspiration and Advances von Beutner, Gregory L, Denmark, Scott E

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Non-Innocent Role of Sacrificial Anodes in Electrochemical Nickel-Catalyzed C(sp 2 )–C(sp 3 ) Cross-Electrophile Coupling von Cardinale, Luana, Beutner, Gregory L., Bemis, Christopher Y., Weix, Daniel J., Stahl, Shannon S.

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Nickel-Catalyzed Synthesis of Quinazolinediones von Beutner, Gregory L, Hsiao, Yi, Razler, Thomas, Simmons, Eric M, Wertjes, William

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Robust Analytical Methods for Monitoring the Formation of a Chiral Oxazaborolidine Catalyst von Ayers, Sloan, Beutner, Gregory L, Ding, Wei, Higman, Carolyn, Pathirana, Charles, Wethman, Robert

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An Evaluation of the Occupational Health Hazards of Peptide Couplers von Graham, Jessica C., Trejo-Martin, Alejandra, Chilton, Martyn L., Kostal, Jakub, Bercu, Joel, Beutner, Gregory L., Bruen, Uma S., Dolan, David G., Gomez, Stephen, Hillegass, Jedd, Nicolette, John, Schmitz, Matthew

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Safety as a Factor in Reaction Development: Considerations of Sensitization Potential with Amide Bond Forming Reagents von George, David T., Williams, Michael J., Beutner, Gregory L.

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Beyond Amide Bond Formation: TCFH as a Reagent for Esterification von Luis, Nathaniel R., Chung, Kasey K., Hickey, Matthew R., Lin, Ziqing, Beutner, Gregory L., Vosburg, David A.

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Catalytic, Enantioselective, Vinylogous Aldol Reactions von Denmark, Scott E., Heemstra Jr, John R., Beutner, Gregory L.

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TCFH–NMI Ketone Synthesis Inspired by Nucleophilicity Scales von Ho, Johnson H., Miller, Grant H., Chung, Kasey K., Neibert, Sydney D., Beutner, Gregory L., Vosburg, David A.

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Palladium-Catalyzed Amidation and Amination of (Hetero)aryl Chlorides under Homogeneous Conditions Enabled by a Soluble DBU/NaTFA Dual-Base System von Beutner, Gregory L, Coombs, John R, Green, Rebecca A, Inankur, Bahar, Lin, Dong, Qiu, Jun, Roberts, Frederick, Simmons, Eric M, Wisniewski, Steven R

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Scalable Synthesis of the Potent HIV Inhibitor BMS-986001 by Non-Enzymatic Dynamic Kinetic Asymmetric Transformation (DYKAT) von Ortiz, Adrian, Benkovics, Tamas, Beutner, Gregory L., Shi, Zhongping, Bultman, Michael, Nye, Jeffrey, Sfouggatakis, Chris, Kronenthal, David R.

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A Divergent Nickel-Catalyzed Synthesis of Quinazolinediones and Benzoxazinone Imines von Wertjes, William, Ayers, Sloan, Gao, Qi, Simmons, Eric M., Beutner, Gregory L.

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Deoxyfluorination of 1°, 2°, and 3° Alcohols by Nonbasic O–H Activation and Lewis Acid-Catalyzed Fluoride Shuttling von Moon, Hye Won, Lavagnino, Marissa N., Lim, Soohyun, Palkowitz, Maximilian D., Mandler, Michael D., Beutner, Gregory L., Drance, Myles J., Lipshultz, Jeffrey M., Scola, Paul M., Radosevich, Alexander T.

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Electroreductive Synthesis of Nickel(0) Complexes von Rubel, Camille Z., Cao, Yilin, El‐Hayek Ewing, Tamara, Laudadio, Gabriele, Beutner, Gregory L., Wisniewski, Steven R., Wu, Xiangyu, Baran, Phil S., Vantourout, Julien C., Engle, Keary M.

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General Method for Quantitation of Organic Hydroperoxides von Beutner, Gregory L, Ayers, Sloan, Chen, Tao, Leung, Simon W, Tai, Hua Chia, Wang, Qinggang

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Direct Lewis Acid Catalyzed Conversion of Enantioenriched N‑Acyloxazolidinones to Chiral Esters, Amides, and Acids von Stevens, Jason M, Parra-Rivera, Ana Cristina, Dixon, Darryl D, Beutner, Gregory L, DelMonte, Albert J, Frantz, Doug E, Janey, Jacob M, Paulson, James, Talley, Michael R

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Facile Amide Bond Formation with TCFH–NMI in an Organic Laboratory Course von M. Baldwin, Oliver W., Conrad-Marut, Linden H., Beutner, Gregory L., Vosburg, David A.

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Lewis Base Activation of Lewis Acids:  Catalytic, Enantioselective Addition of Silyl Ketene Acetals to Aldehydes von Denmark, Scott E, Beutner, Gregory L, Wynn, Thomas, Eastgate, Martin D

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