Figure - available from: Frontiers in Chemistry
This content is subject to copyright.
Download
View publication
Crystal structure of the bismuth(III) acetylide [3] with labeled Bi(1)-C(1), C(1)≡C(2) and C(2)-C(sp²) bonds and transannular Bi(1)-O(1) interaction distances [Å].

Crystal structure of the bismuth(III) acetylide [3] with labeled Bi(1)-C(1), C(1)≡C(2) and C(2)-C(sp²) bonds and transannular Bi(1)-O(1) interaction distances [Å].

Source publication
(A) Recent reports on organobismuth(III) compounds with tethered...
(A) Synthetic route for the synthesis of diphenyl sulfone bismuth(III)...
Crystal structure of the bismuth(III) acetylide [3] with labeled...
Reaction scheme of kinetic studies of copper(I)-catalyzed reaction of...
+9 Cyclic voltammogram of bismuth(III) acetylides in the presence of the...
Electrochemical Studies of the Cycloaddition Activity of Bismuth(III) Acetylides Towards Organic Azides Under Copper(I)-Catalyzed Conditions
Article
Full-text available
  • Feb 2022
Time-dependent monitoring of the reactive intermediates provides valuable information about the mechanism of a synthetic transformation. However, the process frequently involves intermediates with short lifetimes that significantly challenge the accessibility of the desired kinetic data. We report in situ cyclic voltammetry (CV) and nuclear magneti...
Cite
Download full-text

Similar publications

Figure 2. (a) 31 P NMR spectrum of the reaction mixture obtained in the...
Scheme 1. Synthetic routes for the synthesis of tetraethyl...
Scheme 4. Conditions and yields for the synthesis of tetraethyl...
Yields of the Michaelis-Becker-like nucleophilic addition of diethyl...
Screening of reaction conditions in the synthesis of bisphosphonate...
One-Pot and Catalyst-Free Transformation of N-Protected 1-Amino-1-Ethoxyalkylphosphonates into Bisphosphonic Analogs of Protein and Non-Protein α-Amino Acids
Article
Full-text available
  • Jun 2022
Herein, we describe the development of one-pot transformation of α-ethoxy derivatives of phosphorus analogs of protein and non-protein α-amino acids into biologically important N-protected 1-aminobisphosphonates. The proposed strategy, based on the three-component reaction of 1-(N-acylamino)-1-ethoxyphosphonates with triphenylphosphonium tetrafluor...
View