A Study of the Epoxidation of 6-Deoxyhex-5-enopyranosides. 1,5-Dicarbonyl Derivatives and Novel Synthetic Routes to d-xylo-Hexos-5-ulose and d-lyxo-Hexos-5-ulose-Reference-Cited by-同舟云学术

A Study of the Epoxidation of 6-Deoxyhex-5-enopyranosides. 1,5-Dicarbonyl Derivatives and Novel Synthetic Routes to d-xylo-Hexos-5-ulose and d-lyxo-Hexos-5-ulose

Published:2002-04-30 Issue:11 Volume:67 Page:3733-3741
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Enright Philomena M.¹,Tosin Manuela¹,Nieuwenhuyzen Mark¹,Cronin Linda¹,Murphy Paul V.¹

Affiliation:

1. Department of Chemistry, Centre for Synthesis and Chemical Biology, Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin 4, Ireland, and School of Chemistry, Queen's University, Belfast BT9 5AG, Antrim, Northern Ireland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo016378c

Reference25 articles.

1. Glycals in Organic Synthesis: The Evolution of Comprehensive Strategies for the Assembly of Oligosaccharides and Glycoconjugates of Biological Consequence

2. The conversion of carbohydrate derivatives into functionalized cyclohexanes and cyclopentanes

3. Recent Advances in the Conversion of Carbohydrate Furanosides and Pyranosides into Carbocycles

4. Direct Conversion of 5,6-Unsaturated Hexopyranosyl Compounds to Functionalized Cyclohexanones

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