Enzymatic Hydrolysis of Tertiary Amide Bonds by anti Nucleophilic Attack and Protonation-Reference-Cited by-同舟云学术

Enzymatic Hydrolysis of Tertiary Amide Bonds by anti Nucleophilic Attack and Protonation

Published:2018-09-26 Issue:21 Volume:83 Page:13543-13548
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Syrén Per-Olof¹^ORCID

Affiliation:

1. School of Engineering Sciences in Chemistry, Biotechnology and Health, Science for Life Laboratory, Department of Fibre and Polymer Technology, and Department of Protein Science, KTH Royal Institute of Technology, Solna, Sweden 17165

Funder

Svenska Forskningsr?det Formas

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b02053

Reference78 articles.

1. General Olefin Synthesis by the Palladium‐Catalyzed Heck Reaction of Amides: Sterically Controlled Chemoselective NC Activation

2. An N-end rule pathway that recognizes proline and destroys gluconeogenic enzymes

3. Reversible Twisting of Primary Amides via Ground State N–C(O) Destabilization: Highly Twisted Rotationally Inverted Acyclic Amides

4. Nucleophilicities of Primary and Secondary Amines in Water

5. Switching and Conformational Fixation of Amides Through Proximate Positive Charges

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