Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/98450
Type: Artigo de periódico
Title: Determination Of The Absolute Configuration Of Chiral Secondary Alcohols From Tetra-o-acetylglucosidation-induced 1h Nuclear Magnetic Resonance Shifts
Author: Faghih R.
Fontaine C.
Horibe I.
Imamura P.M.
Lukacs G.
Olesker A.
Seo S.
Abstract: Tetra-O-acetylglucosidation-induced 1H nuclear magnetic resonance shifts were found highly characteristic of the absolute configuration of representative examples of A and S chiral secondary alcohols. The most important chemical shift changes of structurally diagnostic value for the determination of the absolute configuration of alcohols concern the protons of the aglycone attached to the carbons at β-position relative to the oxygen atom. © 1985 American Chemical Society.
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Rights: fechado
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Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-0344867952&partnerID=40&md5=27b601b4b84e18952890e96fed917662
Date Issue: 1985
Appears in Collections:Unicamp - Artigos e Outros Documentos

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