Tetrahedron Letters p. 799 - 802 (1995)
Update date:2022-07-30
Topics:
Martin, Olivier R.
Saavedra, Oscar M.
β-Homonojirimycin 2 was prepared in 27% overall yield from tetra-O-benzyl-D-glucono-1,5-lactone by way of the double reductive amination of a 2,6-heptodiulose (7). This synthetic approach provided also access to the 1,N-anhydro derivative of 2, compound 3
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(1951)Doi:10.1002/jhet.2961
(2017)Doi:10.1002/ejoc.201400151
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