Mechanistic Insight into the Catalytic Staudinger Ligation.

Org Lett

Institute for Molecules and Materials , Radboud University, Heyendaalseweg 135 , 6525 AJ Nijmegen , The Netherlands.

Published: February 2019

Organophosphorus-catalyzed Staudinger ligation between carboxylic acids and azides in the presence of phenylsilane reductant produces amides. NMR-based mechanistic investigations revealed that the catalytic Staudinger ligation does not proceed via reduction of phosphine oxide but rather via reduction of iminophosphorane, which can subsequently undergo several transformations to produce the amide product.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.orglett.8b04035DOI Listing

Publication Analysis

Top Keywords

staudinger ligation
12
catalytic staudinger
8
mechanistic insight
4
insight catalytic
4
ligation organophosphorus-catalyzed
4
organophosphorus-catalyzed staudinger
4
ligation carboxylic
4
carboxylic acids
4
acids azides
4
azides presence
4

Similar Publications

The trifluoromethyl (-CF) group represents a highly prevalent functionality in pharmaceuticals. Over the past few decades, significant advances have been made in the development of synthetic methods for trifluoromethylation. In contrast, there are currently no metalloenzymes known to catalyze the formation of C(sp)-CF bonds.

View Article and Find Full Text PDF

Innovative Peptide Bioconjugation Chemistry with Radionuclides: Beyond Classical Click Chemistry.

Pharmaceuticals (Basel)

September 2024

Department of Oncology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB T6G 1Z2, Canada.

: The incorporation of radionuclides into peptides and larger biomolecules requires efficient and sometimes biorthogonal reaction conditions, to which click chemistry provides a convenient approach. : Traditionally, click-based radiolabeling techniques have focused on classical click chemistry, such as copper(I)-catalyzed alkyne-azide [3+2] cycloaddition (CuAAC), strain-promoted azide-alkyne [3+2] cycloaddition (SPAAC), traceless Staudinger ligation, and inverse electron demand Diels-Alder (IEDDA). : However, newly emerging click-based radiolabeling techniques, including tyrosine-click, sulfo-click, sulfur(VI) fluoride exchange (SuFEx), thiol-ene click, azo coupling, hydrazone formations, oxime formations, and RIKEN click offer valuable alternatives to classical click chemistry.

View Article and Find Full Text PDF

Total synthesis, stereochemical assignment, and biological evaluation of opantimycin A and analogues thereof.

Org Biomol Chem

November 2024

Department of Biology, Graduate School of Science, Osaka Metropolitan University, 3-3-138 Sugimoto, Sumiyoshi, Osaka 558-8585, Japan.

Opantimycin A, a rare antimycin-class antibiotic without the macrolide core, was isolated from sp. RK88-1355 in 2017. In this study, we explored the total synthesis and stereochemical assignment of opantimycin A.

View Article and Find Full Text PDF

The germylone dimNHCGe (dimNHC=diimino N-heterocyclic carbene) reacts with azides N R (R=SiMe or p-tolyl) to furnish the first examples of germanium π-complexes, i. e. guanidine-ligated compounds (dimNHI-SiMe )Ge (NHI=N-heterocyclic imine, R=SiMe ) and (dimNHI-Tol)Ge (R=p-tolyl).

View Article and Find Full Text PDF

Synthesis of Peptidyl-tRNA Mimics for Structural Biology Applications.

Acc Chem Res

October 2023

Institute of Organic Chemistry and Center for Molecular Biosciences, University of Innsbruck, Innrain 80-82, 6020 Innsbruck, Austria.

Protein biosynthesis is a central process in all living cells that is catalyzed by a complex molecular machine─the ribosome. This process is termed translation because the language of nucleotides in mRNAs is translated into the language of amino acids in proteins. Transfer RNA (tRNA) molecules charged with amino acids serve as adaptors and recognize codons of mRNA in the decoding center while simultaneously the individual amino acids are assembled into a peptide chain in the peptidyl transferase center (PTC).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!