The reactions of trans-[PtCl₄(RCN)₂] (R= Me, Et, CH₂Ph, Ph) with the diamines and the triamine NH₂{spacer}NH₂ (spacer = CH₂CH₂, CH(Me)CH₂, CH₂CH₂CH₂, CH₂CH₂CH₂CH₂, CH₂CH₂NHCH₂CH₂) in a molar ratio 1 : 2 produce trans-[PtCl₄{NH=C(R)NH{spacer}NH₂}₂] (spacer/R = CH₂CH₂/Et 1, CH₂CHMe/Et 2 (a mixture of regioisomers), CH₂CH₂CH₂/Et 3, CH₂CH₂CH₂CH₂/Et 4, CH₂CH₂/Me 5, CH₂CH₂/CH₂Ph 6, CH₂CH₂/Ph 7, CH₂CH₂NHCH₂CH₂/Et 8) with the monodentately coordinated amidine ligands having the pendant NH₂ groups. The complexes have been characterised by C, H, and N elemental analyses, ¹³C CP-MAS NMR and IR spectroscopy, (TOF)-ESI-MS, and [1·H₂](Pic)₂·EtOH also by X-ray diffraction.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c001103gDOI Listing

Publication Analysis

Top Keywords

one-end nucleophilic
4
nucleophilic addition
4
addition di-
4
di- triamines
4
triamines ptiv-coordinated
4
ptiv-coordinated nitriles
4
nitriles entry
4
entry amidineptiv
4
amidineptiv complexes
4
complexes bearing
4

Similar Publications

Disulfide bridging, also known as disulfide stapling, is a powerful strategy for the construction of site-selective protein bioconjugates. Here we describe the first examples of a new class of such reagents, containing a 'stable-labile' design. These dual-reactive reagents are designed to form a stable bond to one cysteine and a labile bond to the second; resulting in a robust attachment to the protein with one end of the bridge, whilst the other end serves as a reactive handle for subsequent bioconjugation.

View Article and Find Full Text PDF

In the most general practice of asymmetric catalysis, a chiral catalyst, typically bearing a center or an axis of chirality, is employed as the chiral source for imparting enantiocontrol over the developing product. Given the current interest toward optically pure compounds, various forms of chiral induction enabled by diverse chiral sources as well as the use of multiple catalysts under one-pot conditions have been in focus. In one such promising development, an achiral -sulfonamide protected 1,6-amino allyl alcohol (NaphSONHCHC(Ph)CHCH[double bond, length as m-dash]CHCHOH) was subjected to Tsuji-Trost activation and an intramolecular amination to form important chiral pyrrolidine frameworks.

View Article and Find Full Text PDF

Transpeptidation-mediated single-particle imaging assay for sensitive and specific detection of sortase with dark-field optical microscopy.

Biosens Bioelectron

April 2021

Department of Chemistry, Shanghai Stomatological Hospital, State Key Laboratory of Molecular Engineering of Polymers and Institute of Biomedical Sciences, Fudan University, Shanghai, 200433, PR China. Electronic address:

Article Synopsis
  • Transpeptidation catalyzed by sortase is essential for the infection process of Gram-positive bacteria, making it important to monitor its activity and find inhibitors.
  • A new digital imaging method was developed to measure sortase A (SrtA) activity, using gold nanoparticles to visualize and quantify the enzyme's action at a single-particle level.
  • This method shows high sensitivity for detecting SrtA and allows for the testing of various inhibitors, offering a useful analytical tool for research in infection mechanisms and drug development.
View Article and Find Full Text PDF

Two indolocarbazole-naphthyridine foldamers 2 and 3 that fold into helical conformations were prepared. The 4-(N,N-dimethylamino)pyridine (DMAP) moiety was introduced at one end of the foldamer strands to develop foldamer-based catalysts for the site-selective acylation of polyols. These foldamers adopt helical conformations containing internal cavities capable of binding octyl β-d-glucopyranoside.

View Article and Find Full Text PDF

Product template (PT) domains from fungal nonreducing polyketide synthases (NR-PKSs) are responsible for controlling the aldol cyclizations of poly-β-ketone intermediates assembled during the catalytic cycle. Our ability to understand the high regioselective control that PT domains exert is hindered by the inaccessibility of intrinsically unstable poly-β-ketones for in vitro studies. We describe here the crystallographic application of "atom replacement" mimetics in which isoxazole rings linked by thioethers mimic the alternating sites of carbonyls in the poly-β-ketone intermediates.

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!