Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/93073
Type: Artigo de periódico
Title: Concerning The Application Of The1h Nmr Abx Analysis For Assignment Of Stereochemistry To Aldols Deriving From Aldehydes Lacking β-branches
Author: Dias L.C.
Aguilar A.M.
Salles Jr. A.G.
Steil L.J.
Roush W.R.
Abstract: Attempts to apply the 1H NMR ABX method for assignment of stereochemistry of β-hydroxy ketones to aldols 4-10 deriving from α-methyl aldehydes lacking β-branches reveals that the presence of a β-branch in the aldehyde reaction partner is necessary so that the average chemical environment of Ha and Hb is different for the Felkin and anti-Felkin aldols (see conformational pairs A/B and C/D, respectively). When the chiral α-methyl aldehyde lacks a β-branch, as in the case of the aldehyde precursors to 4-10, the conformational energies of E and F (for the Felkin β-hydroxy ketone derivatives), and conformers G and H for the anti-Felkin aldols, are too close in energy (within each pair), such that the average chemical and magnetic environments of Ha and Hb in the two diastereomers cannot be easily distinguished. This analysis provides a rational basis for application of the 1H NMR ABX pattern analysis to other β-hydroxy ketone derivatives. © 2005 American Chemical Society.
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Rights: fechado
Identifier DOI: 10.1021/jo051773e
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-28744431819&partnerID=40&md5=ed7ffb8f91564e1e4aa00369dafd2d15
Date Issue: 2005
Appears in Collections:Unicamp - Artigos e Outros Documentos

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