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 |