Regioselective synthesis of partially protected trehalose analogues and assignment of ring size in isopropylidene acetal derivatives by 13C NMR spectroscopy

Article abstract of DOI:10.1080/07328309608005683

The ¹³C NMR spectra of a range of di-O-isopropylidene acetals of α,α-trehalose and its analogues 1, 2, 4-7 have been studied. Attention has been focussed on the chemical shifts of the acetal carbon and methyl groups of the acetals. These parame

Full text of DOI:10.1080/07328309608005683

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Journal of Carbohydrate Chemistry
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Regioselective Synthesis of Partially
Protected Trehalose Analogues
and Assignment of Ring Size in
Isopropylidene Acetal Derivatives by 13 C
Nmr Spectroscopy
Rafik W. Bassily a , Rimon H Youssef a , Ramadan I. El-Sokkary a
Mina A Nashed a
a Department of Chemistry , Faculty of Science Alexandria
&
University , Ebrahemia, P.O. Box 426, Alexandria, 21321, EGYPT
Published online: 22 Aug 2006.
To cite this article: Rafik W. Bassily , Rimon H Youssef , Ramadan I. El-Sokkary & Mina A Nashed
(1996) Regioselective Synthesis of Partially Protected Trehalose Analogues and Assignment of Ring Size
in Isopropylidene Acetal Derivatives by 13 C Nmr Spectroscopy, Journal of Carbohydrate Chemistry,
15:6, 653-663, DOI: 10.1080/07328309608005683
To link to this article: http://dx.doi.org/10.1080/07328309608005683
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