First asymmetric synthesis of enantiomerically pure (1R,2S)-(-)-(1,2-epoxypropyl)phosphonic acid (fosfomycin)

1989 ◽  
Vol 54 (6) ◽  
pp. 1470-1473 ◽  
Author(s):  
Claudio Giordano ◽  
Graziano Castaldi
2020 ◽  
Vol 24 (8) ◽  
pp. 900-908
Author(s):  
Ram Naresh Yadav ◽  
Amrendra K Singh ◽  
Bimal Banik

Numerous O (oxa)- and S (thia)-glycosyl esters and their analogous glycosyl acids have been accomplished through stereoselective glycosylation of various peracetylated bromo sugar with benzyl glycolate using InBr3 as a glycosyl promotor followed by in situ hydrogenolysis of resulting glycosyl ester. A tandem glycosylating and hydrogenolytic activity of InBr3 has been successfully investigated in a one-pot procedure. The resulting synthetically valuable and virtually unexplored class of β-CMGL (glycosyl acids) could serve as an excellent potential chiral auxiliary in the asymmetric synthesis of a wide range of enantiomerically pure medicinally prevalent β-lactams and other bioactive molecules of diverse medicinal interest.


2007 ◽  
Vol 18 (22) ◽  
pp. 2712-2718 ◽  
Author(s):  
Henryk Krawczyk ◽  
Marcin Śliwiński ◽  
Jacek Kędzia ◽  
Jakub Wojciechowski ◽  
Wojciech M. Wolf

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