Facile Synthesis of (2S,3R,4R)-2-Hydroxymethyl-3,4-pyrrolidinediol and 4-Acetamido-1,2,3-tri-O-acetyl-4-deoxy-l-xylopyranose from the Photoproduct of d-Mannose
- 1 March 1989
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 62 (3) , 797-799
- https://doi.org/10.1246/bcsj.62.797
Abstract
(Synthesis of 2S,3R,4R)-2-hydroxymethyl-3,4-pyrrolidinediol and 4-acetamido-1,2,3-tri-O-acetyl-4-deoxy-l-xylopyranose were attained in four steps from d-mannose, using iron(III)-catalyzed photoreaction as a key reaction.This publication has 6 references indexed in Scilit:
- Total synthesis of amphotericin B. 3. The final stagesJournal of the American Chemical Society, 1988
- Metal-Catalyzed Organic Photoreactions. Iron(III)-Catalyzed Photoreactions of Aldo- and KetohexosesBulletin of the Chemical Society of Japan, 1988
- Improved synthesis of (2R,3S,4R)-3,4-dihydroxy-2-hydroxymethylpyrrolidine derivatives.CHEMICAL & PHARMACEUTICAL BULLETIN, 1988
- Total synthesis of amphotericin BJournal of the American Chemical Society, 1987
- Potent competitive inhibition of α-galactosidase and α-glucosidase activity by 1,4-dideoxy-1,4-iminopentitols: syntheses of 1,4-dideoxy-1,4-imino-d-lyxitol and of both enantiomers of 1,4-dideoxy-1,4-iminoarabinitolTetrahedron Letters, 1985
- Identification of the 2-hydroxymethyl-3,4-dihydroxypyrrolidine (or 1,4-dideoxy-1,4-iminopentitol) from and from as the (2R, 3R, 4S)-isomer by the synthesis of its enantiomer.Tetrahedron Letters, 1985