Title of article
Structural determination of mannopeptimycin cyclic acetals
Author/Authors
He، نويسنده , , Haiyin and Wang، نويسنده , , Ting-Zhong and Dushin، نويسنده , , Russell G and Feng، نويسنده , , Xidong and Shen، نويسنده , , Bo and Ashcroft، نويسنده , , Joseph S and Koehn، نويسنده , , Frank E and Carter، نويسنده , , Guy T، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2004
Pages
5
From page
5889
To page
5893
Abstract
In structure–activity relationship (SAR) studies on mannopeptimycin antibiotics, mannopeptimycin α(1) was acetalized by reacting with certain dialkyl acetals under acidic conditions. The major products of these reactions were determined to be cyclic acetals at the 4,6-positions of the terminal mannose (Man-B), by exemplary spectroscopic analyses of two typical acetalization products 2 and 3.
Journal title
Tetrahedron Letters
Serial Year
2004
Journal title
Tetrahedron Letters
Record number
1842791
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