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Some Studies on Carbonyl Radical Cyclizations and on the Synthesis of 2-Deoxy-β-D-Glycosides by Stereoselective Radical Reactions
| Content Provider | Semantic Scholar |
|---|---|
| Author | Crich, David Fortt, Simon M. Ritchie, Timothy J. |
| Copyright Year | 1989 |
| Abstract | The effect of substituents on the mode (exo- or endo-) and efficiency of 6, 7-olefinic carbonyl radical cyclizations has been studied. A new method for the synthesis of 2-deoxy-β-D-glycosides, in which the key step is a stereoselective radical decarboxylation, has been developed. |
| Starting Page | 135 |
| Ending Page | 143 |
| Page Count | 9 |
| File Format | PDF HTM / HTML |
| DOI | 10.1007/978-94-009-0897-0_12 |
| Volume Number | 21 |
| Alternate Webpage(s) | https://page-one.springer.com/pdf/preview/10.1007/978-94-009-0897-0_12 |
| Alternate Webpage(s) | https://doi.org/10.1007/978-94-009-0897-0_12 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |