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ChemInform Abstract: The First Synthesis of All Possible Stereoisomers of the (E)-4,5- Dihydroxydec-2-enal, in Homochiral Form.

โœ Scribed by P. ALLEVI; P. CIUFFREDA; G. TAROCCO; M. ANASTASIA


Book ID
112027376
Publisher
John Wiley and Sons
Year
2010
Weight
30 KB
Volume
27
Category
Article
ISSN
0931-7597

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The first synthesis of all possible ster
โœ Pietro Allevi; Pierangela Ciuffreda; Giorgio Tarocco; Mario Anastasia ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 465 KB

The first synthesis of the four possible isomers of (E)-4,5-dihydroxydec-2-enal, a cytotoxic product ofmicrosomal lipid peroxidation, is accomplished starting with D-and Larabinose, D-ribose and D-lyxose by an identical reaction sequence. Each pentose was diacetonised and subjected to a Wittig react