On-Demand Complex Peptide Synthesis: An Aspirational (and Elusive?) Goal for Peptide Synthesis von Schwieter, Kenneth E, Johnston, Jeffrey N

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Expanding the limits of the second genetic code with ribozymes von Lee, Joongoo, Schwieter, Kenneth E., Watkins, Andrew M., Kim, Do Soon, Yu, Hao, Schwarz, Kevin J., Lim, Jongdoo, Coronado, Jaime, Byrom, Michelle, Anslyn, Eric V., Ellington, Andrew D., Moore, Jeffrey S., Jewett, Michael C.

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Charge Transport in Sequence-Defined Conjugated Oligomers von Yu, Hao, Li, Songsong, Schwieter, Kenneth E, Liu, Yun, Sun, Boran, Moore, Jeffrey S, Schroeder, Charles M

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A one-pot amidation of primary nitroalkanes von Schwieter, Kenneth E, Johnston, Jeffrey N

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Enantioselective Addition of Bromonitromethane to Aliphatic N‑Boc Aldimines Using a Homogeneous Bifunctional Chiral Organocatalyst von Schwieter, Kenneth E, Johnston, Jeffrey N

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Umpolung Amide Synthesis Using Substoichiometric N‑Iodosuccinimide (NIS) and Oxygen as a Terminal Oxidant von Schwieter, Kenneth E, Shen, Bo, Shackleford, Jessica P, Leighty, Matthew W, Johnston, Jeffrey N

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Enantioselective Synthesis of D-α-Amino Amides from Aliphatic Aldehydes von Schwieter, Kenneth E, Johnston, Jeffrey N

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Preparation of H,(4) PyrrolidineQuin-BAM (PBAM) von Davis, Tyler A, Dobish, Mark C, Schwieter, Kenneth E, Chun, Aspen C, Johnston, Jeffrey N

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A one-pot amidation of primary nitroalkanesElectronic supplementary information (ESI) available: Experimental procedures and spectroscopic data for all new compounds. See DOI: 10.1... von Schwieter, Kenneth E, Johnston, Jeffrey N

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Enantioselective synthesis of d-α-amino amides from aliphatic aldehydesElectronic supplementary information (ESI) available. See DOI: 10.1039/c5sc00064e von Schwieter, Kenneth E, Johnston, Jeffrey N

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Enantioselective synthesis of d-α-amino amides from aliphatic aldehydes† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c5sc00064e Click here for additiona... von Schwieter, Kenneth E., Johnston, Jeffrey N.

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ChemInform Abstract: A One‐Pot Amidation of Primary Nitroalkanes von Schwieter, Kenneth E., Johnston, Jeffrey N.

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ChemInform Abstract: Umpolung Amide Synthesis Using Substoichiometric N-Iodosuccinimide (NIS) and Oxygen as a Terminal Oxidant von Schwieter, Kenneth E., Shen, Bo, Shackleford, Jessica P., Leighty, Matthew W., Johnston, Jeffrey N.

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Preparation of H,4 PyrrolidineQuin-BAM (PBAM) von Davis, Tyler A., Dobish, Mark C., Schwieter, Kenneth E., Chun, Aspen C., Johnston, Jeffrey N.

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EXPANDING THE CHEMICAL SUBSTRATES FOR GENETIC CODE REPROGRAMMING von Jewett, Michael Christopher, Moore, Jeffrey S, Lee, Joongoo, Schwieter, Kenneth E, Schwarz, Kevin Jerome

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Expanding the chemical substrates for genetic code reprogramming von Jewett, Michael Christopher, Moore, Jeffrey S, Lee, Joongoo, Schwieter, Kenneth E, Schwarz, Kevin Jerome

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ChemInform Abstract: Enantioselective Synthesis of D-α-Amino Amides from Aliphatic Aldehydes von Schwieter, Kenneth E., Johnston, Jeffrey N.

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ChemInform Abstract: Enantioselective Synthesis of D-[alpha]-Amino Amides from Aliphatic Aldehydes von Schwieter, Kenneth E, Johnston, Jeffrey N

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Expanding the Chemical Substrates for Genetic Code Reprogramming von Jewett, Michael Christopher, Moore, Jeffrey S, Lee, Joongoo, Schwieter, Kenneth E, Schwarz, Kevin Jerome

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EXPANDING THE CHEMICAL SUBSTRATES FOR GENETIC CODE REPROGRAMMING von JEWETT, Michael Christopher, LEE, Joongoo, SCHWARZ, Kevin Jerome, MOORE, Jeffrey S, SCHWIETER, Kenneth E

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