Synthesis of 2 (R), 5 (R)-bis (hydroxymethyl)-3 (R), 4 (R)-dihydroxypyrrolidine. A novel glycosidase inhibitor
PJ Card, WD Hitz
Index: Card, Peter J.; Hitz, William D. Journal of Organic Chemistry, 1985 , vol. 50, # 6 p. 891 - 893
Full Text: HTML
Citation Number: 55
Abstract
Pyrrolidine 3 with absolute configuration as indicated represents a challenging synthetic target because of its four contiguous asymmetric centers. We chose L-sorbose as our starting material because it contains the desired absolute configuration at C-3 and C-4 and the opposite configuration at C-5 that would be inverted upon substitution by a nitrogen nucleophile. Subsequent ring closure via attack of the nitrogen upon C-2 followed by ...
Related Articles:
[Fleet, George W. J.; Smith, Paul W. Tetrahedron, 1987 , vol. 43, # 5 p. 971 - 978]
[Bouillon, Marc E.; Pyne, Stephen G. Tetrahedron Letters, 2014 , vol. 55, # 2 p. 475 - 478]
[Le Merrer, Yves; Poitout, Lydie; Depezay, Jean-Claude; Dosbaa, Isabelle; Geoffroy, Sabine; Foglietti, Marie-Jose Bioorganic and Medicinal Chemistry, 1997 , vol. 5, # 3 p. 519 - 533]
[Organic Letters, , vol. 8, # 2 p. 297 - 299]
[Organic Letters, , vol. 8, # 2 p. 297 - 299]