Campagne, J.-M.  et al.: 2024 Science of Synthesis, 2024/2: Knowledge Updates 2024/2 DOI: 10.1055/sos-SD-122-00254
Knowledge Updates 2024/2

22.3.5 Tellurocarboxylic Acids and Derivatives (Update 2024)

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Book

Editors: Campagne, J.-M. ; Donohoe, T. J.; Jiang, X. ; Wang, M.

Authors: Cellnik, T. ; de Figueiredo, R. M. ; Deng, G.-J. ; Dong, K. ; Healy, A. ; Huang, H. ; Ji, X. ; Jo, W. ; Manisha ; Murai, T. ; Parmar, D. ; Sawamura, M. ; Sharma, U. ; Shimizu, Y. ; Sumit ; Yang, Z.

Title: Knowledge Updates 2024/2

Online ISBN: 9783132457065; Book DOI: 10.1055/b000000968

Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry

Science of Synthesis Knowledge Updates



Parent publication

Title: Science of Synthesis

DOI: 10.1055/b-00000101

Series Editors: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.

Type: Multivolume Edition

 


Abstract

Tellurocarboxylic acids and their derivatives are tellurium isologues of carboxylic acids, esters, amides, carbonates, and carbamates wherein an oxygen atom of the C=O group in the original compounds is replaced with a tellurium atom. Their stabilities are generally low, and almost no new synthetic methods for them have been reported recently, although some theoretical studies have been published. Nevertheless, iminium salts generated from amides and selenoiminium salts are converted into telluroamides with a tellurating agent prepared from elemental tellurium and lithium aluminum hydride.

 
  • 4 Jaufeerally NB, Abdallah HH, Ramasami P, Schaefer III HF. Theor. Chem. Acc. 2012; 131: 1127 erratum, Theor. Chem. Acc. 2012; 131: 1258