| |
|
|
|
|
|
|
|
|
1. |
Record Nr. |
UNINA9910557258403321 |
|
|
Autore |
Hoenigl Martin |
|
|
Titolo |
HIV-Associated Immune Activation and Persistent Inflammation |
|
|
|
|
|
Pubbl/distr/stampa |
|
|
|
|
|
|
Descrizione fisica |
|
1 online resource (147 p.) |
|
|
|
|
|
|
Soggetti |
|
Immunology |
Medicine and Nursing |
|
|
|
|
|
|
|
|
Lingua di pubblicazione |
|
|
|
|
|
|
Formato |
Materiale a stampa |
|
|
|
|
|
Livello bibliografico |
Monografia |
|
|
|
|
|
Sommario/riassunto |
|
This eBook is a collection of articles from a Frontiers Research Topic. Frontiers Research Topics are very popular trademarks of the Frontiers Journals Series: they are collections of at least ten articles, all centered on a particular subject. With their unique mix of varied contributions from Original Research to Review Articles, Frontiers Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author by contacting the Frontiers Editorial Office: frontiersin.org/about/contact |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
2. |
Record Nr. |
UNINA9910566464703321 |
|
|
Autore |
Aronica Laura Antonella |
|
|
Titolo |
Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles |
|
|
|
|
|
|
|
Pubbl/distr/stampa |
|
|
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
|
|
|
|
|
|
|
Descrizione fisica |
|
1 online resource (124 p.) |
|
|
|
|
|
|
Soggetti |
|
Chemistry |
Organic chemistry |
Research and information: general |
|
|
|
|
|
|
|
|
Lingua di pubblicazione |
|
|
|
|
|
|
Formato |
Materiale a stampa |
|
|
|
|
|
Livello bibliografico |
Monografia |
|
|
|
|
|
Sommario/riassunto |
|
This book is focused on metal-catalyzed cyclocarbonylation reactions applied to the synthesis of heterocyclic rings of different sizes, including diastereoselective and enantioselective approaches, homogeneous and heterogeneous metal catalysis, and the application of these reactions to the total synthesis of natural products. |
|
|
|
|
|
|
|
| |