Stereoselective reactions of alkenylpyranosides: the effect of double bond geometry on conformation
- 1 June 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 110 (12) , 3925-3929
- https://doi.org/10.1021/ja00220a034
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- On the side-chain conformation of N-acetylneuraminic acid and its epimers at C-7, C-8, and C-7,8Carbohydrate Research, 1987
- Deoxy‐nitrosugars 15th communication Synthesis of N‐acetylneuraminic acid and N‐acetyl‐4‐epineuraminic AcidHelvetica Chimica Acta, 1986
- Higher-carbon sugars. Part 2. The synthesis of some decitols via the osmylation of unsaturated precursorsJournal of the Chemical Society, Perkin Transactions 1, 1986
- Higher-carbon sugars. Part 1. The synthesis of some octose sugars via the osmylation of unsaturated precursorsJournal of the Chemical Society, Perkin Transactions 1, 1986
- Barriers to rotation adjacent to double bondsJournal of the American Chemical Society, 1985
- A totally synthetic route to lincosamine: some observations on the diastereofacial selectivity of electrophilic reactions on the double bonds of various 5-(1-alkenyl)arabinopyranosidesJournal of the American Chemical Society, 1985
- Total synthesis of (.+-.)-3-deoxy-D-manno-2-octulopyranosateJournal of the American Chemical Society, 1985
- Strukturelle Abwandlungen anN-Acetylneuraminsäure, 3Monatshefte für Chemie / Chemical Monthly, 1985