Allenone-Mediated Racemization/Epimerization-Free Peptide Bond Formation and Its Application in Peptide Synthesis

Journal of the American Chemical Society ◽

10.1021/jacs.1c04614 ◽

2021 ◽

Author(s):

Zhengning Wang ◽

Xuewei Wang ◽

Penghui Wang ◽

Junfeng Zhao

Keyword(s):

Peptide Synthesis ◽

Bond Formation ◽

Peptide Bond ◽

Peptide Bond Formation ◽

Free Peptide

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Allenone-Mediated Racemization/Epimerization-Free Peptide Bond Formation and Its Application in Peptide Synthesis

Chinese Journal of Organic Chemistry ◽

10.6023/cjoc202100073 ◽

2021 ◽

Vol 41 (10) ◽

pp. 4094

Author(s):

Hua Zhao ◽

Yufen Zhao

Keyword(s):

Peptide Synthesis ◽

Bond Formation ◽

Peptide Bond ◽

Peptide Bond Formation ◽

Free Peptide

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ChemInform Abstract: N-METHYLAMINO ACIDS IN PEPTIDE SYNTHESIS PART 4, RACEMIZATION AND YIELDS IN PEPTIDE-BOND FORMATION

Chemischer Informationsdienst ◽

10.1002/chin.197344459 ◽

1973 ◽

Vol 4 (44) ◽

pp. no-no

Author(s):

JOHN R. MCDERMOTT ◽

N. LEO BENOITON

Keyword(s):

Peptide Synthesis ◽

Bond Formation ◽

Peptide Bond ◽

Peptide Bond Formation

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Peptide Synthesis in Aqueous Environments: The Role of Extreme Conditions on Peptide Bond Formation and Peptide Hydrolysis

Journal of the American Chemical Society ◽

10.1021/ja9032742 ◽

2009 ◽

Vol 131 (38) ◽

pp. 13668-13675 ◽

Cited By ~ 28

Author(s):

Eduard Schreiner ◽

Nisanth N. Nair ◽

Dominik Marx

Keyword(s):

Peptide Synthesis ◽

Bond Formation ◽

Peptide Bond ◽

Extreme Conditions ◽

Peptide Bond Formation ◽

Peptide Hydrolysis ◽

Aqueous Environments

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ChemInform Abstract: FORMATION OF N-ACYL DERIVATIVES OF N,N′-DISUBSTITUTED UREA IN THE REACTION OF PEPTIDE BOND FORMATION BY THE CARBODIIMIDE METHOD. PART V. USE OF N,N′-DIISOPROPYLCARBODIIMIDE IN PEPTIDE SYNTHESIS

Chemischer Informationsdienst ◽

10.1002/chin.198046326 ◽

1980 ◽

Vol 11 (46) ◽

Author(s):

J. IZDEBSKI ◽

D. KUNCE ◽

S. DRABAREK

Keyword(s):

Peptide Synthesis ◽

Bond Formation ◽

Peptide Bond ◽

Peptide Bond Formation ◽

Carbodiimide Method ◽

Derivatives Of ◽

Acyl Derivatives

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Faculty Opinions recommendation of Important contribution to catalysis of peptide bond formation by a single ionizing group within the ribosome.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1008921.111307 ◽

2002 ◽

Author(s):

Jon Lorsch

Keyword(s):

Bond Formation ◽

Peptide Bond ◽

Peptide Bond Formation

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Faculty Opinions recommendation of Substrate-assisted catalysis of peptide bond formation by the ribosome.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1022150.326474 ◽

2005 ◽

Author(s):

Alfred Wittinghofer

Keyword(s):

Bond Formation ◽

Peptide Bond ◽

Peptide Bond Formation

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Faculty Opinions recommendation of An induced-fit mechanism to promote peptide bond formation and exclude hydrolysis of peptidyl-tRNA.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1029397.349450 ◽

2005 ◽

Author(s):

Andrea Barta

Keyword(s):

Bond Formation ◽

Peptide Bond ◽

Peptide Bond Formation ◽

Induced Fit ◽

Hydrolysis Of

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Faculty Opinions recommendation of Quality control by the ribosome following peptide bond formation.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1147301.793492186 ◽

2014 ◽

Author(s):

Eric Westhof

Keyword(s):

Quality Control ◽

Bond Formation ◽

Peptide Bond ◽

Peptide Bond Formation

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Faculty Opinions recommendation of Slow peptide bond formation by proline and other N-alkylamino acids in translation.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1147285.604438 ◽

2009 ◽

Author(s):

Koreaki Ito

Keyword(s):

Bond Formation ◽

Peptide Bond ◽

Peptide Bond Formation

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Beyond peptide bond formation: the versatile role of condensation domains in natural product biosynthesis

Natural Product Reports ◽

10.1039/d0np00098a ◽

2021 ◽

Author(s):

Sofie Dekimpe ◽

Joleen Masschelein

Keyword(s):

Natural Product ◽

Bond Formation ◽

Peptide Bond ◽

Chemical Diversity ◽

Peptide Bond Formation ◽

Natural Product Biosynthesis

Condensation domains perform highly diverse functions during natural product biosynthesis and are capable of generating remarkable chemical diversity.

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