Please use this identifier to cite or link to this item:
192.168.6.56/handle/123456789/75509Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.editor | Di Iorio, Nicola | - |
| dc.date.accessioned | 2019-07-08T07:27:10Z | - |
| dc.date.available | 2019-07-08T07:27:10Z | - |
| dc.date.issued | 2018 | - |
| dc.identifier.isbn | 978-3-319-74914-3 | - |
| dc.identifier.uri | http://10.6.20.12:80/handle/123456789/75509 | - |
| dc.description | All the work discussed in this thesis was done for two possible purposes: either to develop a new reactivity or to achieve a specific structural feature in the product molecule (or both at the same time). However, regardless of the purpose we had for every project, the tool we employed to reach our target was always asymmetric organocatalysis | en |
| dc.language | en | en |
| dc.language.iso | en | en_US |
| dc.publisher | Springer International Publishing AG | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | New Organocatalytic Strategies for the Selective Synthesis of Centrally and Axially Chiral Molecules | en_US |
| dc.type | Book | en_US |
| Appears in Collections: | Chemistry | |
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