Se-77 and Te-125 NMR spectroscopy for enantiopurity determination of chalcogen amines

Oliveira, Samuel S.; Cunha, Rodrigo L. O. R.; Silva, Marcio S.

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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Se-77 and Te-125 NMR spectroscopy for enantiopurity determination of chalcogen amines

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Author(s):	Oliveira, Samuel S. ; Cunha, Rodrigo L. O. R. ; Silva, Marcio S. Total Authors: 3
Document type:	Journal article
Source:	Tetrahedron Letters; v. 57, n. 41, p. 4556-4559, OCT 12 2016.
Web of Science Citations:	5
Abstract
A simple three-component chiral derivatizing protocol for determining the enantiopurity of chalcogen amines by H-1, Se-77 and Te-125 NMR spectroscopy is described. The method involves the formation of a chalcogen-imino-boronate ester complex by the coupling of racemic chalcogen amines, 2-formylphenylboronic acid and optically active (+)-BINOL. The chalcogen primary amines were synthesized by a non active aziridine ring-opening reaction and chalcogen nucleophilic species. (C) 2016 Elsevier Ltd. All rights reserved. (AU)

FAPESP's process:	14/23362-8 - Nuclear magnetic resonance to design and chiral discrimination of biocatalytic process
Grantee:	Márcio Santos da Silva
Support Opportunities:	Regular Research Grants

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