The Ferrier rearrangement as the key step in the synthesis of C <inf>7</inf> -C <inf>16</inf> -alkyl 2,3-dideoxy glucosides from glucose and C <inf>7</inf> -C <inf>16</inf> -alkanols <sup>1-3</sup>

Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/12698

Title:	The Ferrier rearrangement as the key step in the synthesis of C <inf>7</inf> -C <inf>16</inf> -alkyl 2,3-dideoxy glucosides from glucose and C <inf>7</inf> -C <inf>16</inf> -alkanols <sup>1-3</sup>
Authors:	Konstantinović S. Predojević J. Gojković S. Pavlović V. Čanadi, Janoš
Issue Date:	1-Jan-2001
Journal:	Journal of the Serbian Chemical Society
Abstract:	The Ferrier rearrangment was used as the key step in the synthesis of C 7 C 16 -alkyl 2,3-dideoxy glucosides from glucose and C 7 -C 16 -alkanols.
URI:	https://open.uns.ac.rs/handle/123456789/12698
ISSN:	03525139
Appears in Collections:	Naučne i umetničke publikacije

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