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ChemInform Abstract: Study of the Reactivity of [Hydroxy(tosyloxy)iodo]benzene Toward Enol Esters to Access α‐Tosyloxy Ketones.

Title: ChemInform Abstract: Study of the Reactivity of [Hydroxy(tosyloxy)iodo]benzene Toward Enol Esters to Access α‐Tosyloxy Ketones.
Authors: Basdevant, Benoit; Legault, Claude Y.
Source: ChemInform ; volume 46, issue 45 ; ISSN 0931-7597 1522-2667
Publisher Information: Wiley
Publication Year: 2015
Collection: Wiley Online Library (Open Access Articles via Crossref)
Description: Aromatic, aliphatic, and cyclic enol acetates can act as ketone surrogates and are rapidly converted by HTIB (II) to give the corresponding α‐tosyloxy ketones in high yields.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1002/chin.201545044
Availability: https://doi.org/10.1002/chin.201545044; https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchin.201545044; https://onlinelibrary.wiley.com/doi/pdf/10.1002/chin.201545044
Rights: http://onlinelibrary.wiley.com/termsAndConditions#vor
Accession Number: edsbas.8BA9A6D5
Database: BASE