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1. |
Record Nr. |
UNISA990003238780203316 |
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Autore |
TERZANI, Sergio |
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Titolo |
Il bilancio consolidato : con appendice su alcune regolamentazioni straniere in materia di gruppi aziendali e di bilanci consolidati / Sergio Terzani |
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Pubbl/distr/stampa |
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ISBN |
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Descrizione fisica |
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Collana |
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Collana di studi economico-aziendali ; 14 |
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Disciplina |
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Soggetti |
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Bilancio - Consalidamento |
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Collocazione |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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2. |
Record Nr. |
UNINA9910420949003321 |
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Autore |
Matsuoka Junpei |
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Titolo |
Total synthesis of indole alkaloids : based on direct construction of pyrrolocarbazole scaffolds via gold-catalyzed cascade cyclizations / / Junpei Matsuoka |
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Pubbl/distr/stampa |
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Singapore : , : Springer, , [2020] |
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©2020 |
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ISBN |
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Edizione |
[1st ed. 2020.] |
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Descrizione fisica |
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1 online resource (XII, 82 p. 77 illus., 4 illus. in color.) |
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Collana |
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Disciplina |
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Soggetti |
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Indole - Synthesis |
Catalysis |
Chemistry, Inorganic |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Nota di bibliografia |
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Includes bibliographical references. |
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Nota di contenuto |
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1. Introduction -- 2. Total Synthesis of Dictyodendrin A–F by the Gold-Catalyzed Cascade Cyclization of Conjugated Diynes with Pyrroles -- 3. Construction of the Pyrrolo[2,3-d]carbazole Core of Spiroindoline Alkaloids by Gold-Catalyzed Cascade Cyclization of Ynamide. |
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Sommario/riassunto |
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This book explores efficient syntheses of indole alkaloids based on gold-catalyzed cascade cyclizations, presenting two strategies for total synthesis of these natural products based on gold-catalyzed reactions of conjugated diyne or ynamide. The book first describes the total and formal synthesis of dictyodendrins A–F based on direct construction of the pyrrolo[2,3-c]carbazole core using the gold-catalyzed annulation of azido-diynes and protected pyrrole. This synthetic strategy features late-stage functionalization of the pyrrolo[2,3-c]carbazole scaffold at several positions and allows diverse access to dictyodendrins and their derivatives. Secondly, the book discusses the formal synthesis of vindorosine based on the pyrrolo[2,3-d]carbazole construction using the gold-catalyzed cascade cyclization of ynamide. Importantly, the reaction using a chiral gold complex provides the optically active pyrrolo[2,3-d]carbazole. This strategy facilitates the rapid construction of the pyrrolocarbazole core structure of aspidosperma and related |
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alkaloids, including vindorosine. These methodologies can accelerate the medicinal application of pyrrolocarbazole-type alkaloids and related compounds. |
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3. |
Record Nr. |
UNINA9910298986603321 |
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Titolo |
Software Technologies : 8th International Joint Conference, ICSOFT 2013, Reykjavik, Iceland, July 29-31, 2013, Revised Selected Papers / / edited by José Cordeiro, Marten van Sinderen |
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Pubbl/distr/stampa |
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Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 |
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ISBN |
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Edizione |
[1st ed. 2014.] |
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Descrizione fisica |
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1 online resource (XII, 323 p. 95 illus.) |
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Collana |
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Communications in Computer and Information Science, , 1865-0937 ; ; 457 |
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Disciplina |
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Soggetti |
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Software engineering |
Compilers (Computer programs) |
Computer simulation |
Software Engineering |
Compilers and Interpreters |
Computer Modelling |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Bibliographic Level Mode of Issuance: Monograph |
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Nota di contenuto |
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Software paradigm trends -- Mainstream software engineering -- Applications. |
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Sommario/riassunto |
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This book constitutes the thoroughly refereed proceedings of the 8th International Joint Conference on Software Technologies, ICSOFT 2013, held in Reykjavik, Iceland, in July 2013. The 19 revised full papers presented were carefully reviewed and selected from 121 paper submissions. The papers focus on the following research topics and applications: new software paradigm trends and mainstream software engineering and applications. |
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