Acylation Reactions Mediated by Tantalum Carboxylates

Kiran Joshi; Jiang Bao; Alan S. Goldman; Joachim Kohn

doi:10.1021/ja00043a006

Acylation Reactions Mediated by Tantalum Carboxylates

Kiran Joshi, Jiang Bao, Alan S. Goldman, Joachim Kohn

Rutgers University

Research output: Contribution to journal › Article

19 Citations (Scopus)

Abstract

Facile nucleophilic attack on coordinated carboxylate ligands is reported: complexes of tantalum(V) react rapidly with amines and amino acid esters to give the corresponding amides. Cyclopentadienyltantalum(V) amino acid carboxylate complexes have been prepared and reacted with free amino acid esters to give dipeptides in good yield and with high stereochemical purity.

Original language	English
Pages (from-to)	6649-6652
Number of pages	4
Journal	Journal of the American Chemical Society
Volume	114
Issue number	17
DOIs	https://doi.org/10.1021/ja00043a006
Publication status	Published - Aug 1 1992

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ASJC Scopus subject areas

Catalysis
Chemistry(all)
Biochemistry
Colloid and Surface Chemistry

Cite this

Joshi, K., Bao, J., Goldman, A. S., & Kohn, J. (1992). Acylation Reactions Mediated by Tantalum Carboxylates. Journal of the American Chemical Society, 114(17), 6649-6652. https://doi.org/10.1021/ja00043a006

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Access to Document

10.1021/ja00043a006