Synthesis and Lipase-Catalyzed Resolution of 5-(Hydroxymethyl)-1,3-dioxolan-4-ones: Masked Glycerol Analogs as Potential Building Blocks for Pharmaceuticals-Reference-Cited by-同舟云学术

Synthesis and Lipase-Catalyzed Resolution of 5-(Hydroxymethyl)-1,3-dioxolan-4-ones: Masked Glycerol Analogs as Potential Building Blocks for Pharmaceuticals

Published:1996-01-01 Issue:10 Volume:61 Page:3423-3427
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hof Robert P.¹,Kellogg Richard M.¹

Affiliation:

1. Department of Organic and Molecular Inorganic Chemistry, University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo952021v

Reference24 articles.

1. For a review of the use of 2,3-O-isopropylideneglyceraldehyde as a chiral C3-synthon in stereoselective organic synthesis see: Jurczak, J; Pikul, S.; Bauer, T.Tetrahedron1986,42, 447.

2. STUDIES ON ACETONE-GLYCERALDEHYDE

3. Lipase-Catalyzed Resolution of Glycerol 2,3-Carbonate

4. (b) Parmar, V. S.; Prasad, A. K.; Singh, P. K.; Gupta, S.Tetrahedron: Asymmetry1992,3, 1395.

5. Lipase-catalysed transesterification in the preparation of optically active solketal

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