1.

Record Nr.

UNISA990003238780203316

Autore

TERZANI, Sergio

Titolo

Il bilancio consolidato : con appendice su alcune regolamentazioni straniere in materia di gruppi aziendali e di bilanci consolidati / Sergio Terzani

Pubbl/distr/stampa

Pisa : C. Cursi, [1966?]

ISBN

88-13-17047-5

Descrizione fisica

XV, 243 p. ; 25 cm

Collana

Collana di studi economico-aziendali ; 14

Disciplina

658.15

Soggetti

Bilancio - Consalidamento

Collocazione

658.15 TER 1

Lingua di pubblicazione

Italiano

Formato

Materiale a stampa

Livello bibliografico

Monografia



2.

Record Nr.

UNINA9910420949003321

Autore

Matsuoka Junpei

Titolo

Total synthesis of indole alkaloids : based on direct construction of pyrrolocarbazole scaffolds via gold-catalyzed cascade cyclizations / / Junpei Matsuoka

Pubbl/distr/stampa

Singapore : , : Springer, , [2020]

©2020

ISBN

981-15-8652-7

Edizione

[1st ed. 2020.]

Descrizione fisica

1 online resource (XII, 82 p. 77 illus., 4 illus. in color.)

Collana

Springer theses

Disciplina

547.593

Soggetti

Indole - Synthesis

Catalysis

Chemistry, Inorganic

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Nota di bibliografia

Includes bibliographical references.

Nota di contenuto

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.

Sommario/riassunto

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



alkaloids, including vindorosine. These methodologies can accelerate the medicinal application of pyrrolocarbazole-type alkaloids and related compounds.

3.

Record Nr.

UNINA9910298986603321

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

Pubbl/distr/stampa

Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014

ISBN

9783662449202

366244920X

Edizione

[1st ed. 2014.]

Descrizione fisica

1 online resource (XII, 323 p. 95 illus.)

Collana

Communications in Computer and Information Science, , 1865-0937 ; ; 457

Disciplina

005.1

Soggetti

Software engineering

Compilers (Computer programs)

Computer simulation

Software Engineering

Compilers and Interpreters

Computer Modelling

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Note generali

Bibliographic Level Mode of Issuance: Monograph

Nota di contenuto

Software paradigm trends -- Mainstream software engineering -- Applications.

Sommario/riassunto

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.