| dc.contributor.author | Soraya Shafawati Mohamad Tahier | |
| dc.date.accessioned | 2017-04-02T01:25:20Z | |
| dc.date.available | 2017-04-02T01:25:20Z | |
| dc.date.issued | 2013 | |
| dc.identifier.uri | http://hdl.handle.net/123456789/5121 | |
| dc.description.abstract | The cycloaddition reaction is one of the most attractive synthetic protocols for accessing a variety of scienfifically interesting and pharmaceutically useful ring skeletons and efficient method to generate cyclic compounds from simple starting materials | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Japan : Kanazawa University | en_US |
| dc.relation.ispartofseries | ;QD 281 .R5 S6 2013 | |
| dc.subject | QD 281 .R5 S6 2013 | en_US |
| dc.subject | Soraya Shafawati Mohamad Tahier | en_US |
| dc.subject | Tesis Kanazawa University 2013 | en_US |
| dc.subject | Ring formation (Chemistry) | en_US |
| dc.title | Rh(I)-Catalyzed carbonylative [2+2+1] cycloaddition of bis(allene)s toward syntheses of natural products having (m-8-5) tricyclic ring systems | en_US |
| dc.type | Thesis | en_US |