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1. |
Record Nr. |
UNINA9910453063303321 |
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Titolo |
Interdisciplinary contributions for collaborative networks [[electronic resource] /] / guest editors, Rob Dekkers and Hermann Kühnle |
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Pubbl/distr/stampa |
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[Bradford], : Emerald Group Pub. Ltd., 2012 |
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ISBN |
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1-78190-466-9 |
1-283-99115-2 |
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Descrizione fisica |
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1 online resource (195 p.) |
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Collana |
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Journal of manufacturing technology management, , 1741-038X ; ; v. 23, no. 8 |
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Altri autori (Persone) |
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DekkersRob |
KühnleH (Hermann) |
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Disciplina |
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Soggetti |
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Information networks |
Electronic books. |
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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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Description based upon print version of record. |
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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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Cover; CONTENTS; EDITORIAL REVIEW BOARD; Some thoughts on interdisciplinarity in collaborative networks' research and manufacturing sciences; The inter-disciplinary modelling of supply chains in the context of collaborative multi-structural cyber-physical networks; Entropy assessment of supply chain disruption; A model to determine complexity in supply networks; Alignment prediction in collaborative networks; Habitual domain exploration in inter-firm networks; Towards the explanation of goal-oriented and opportunity-based networks of organizations |
Appraising interdisciplinary contributions to theory for collaborative (manufacturing) networksLessons learned from the lifecycle management of collaborative enterprises networks |
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Sommario/riassunto |
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Scientific progress on a field is mostly discussed within disciplines. Far less attention is paid to outside or between disciplines' work. To speed up research progresses for Collaborative Networks in Manufacturing, a base for further grounded theory establishment is propagated recalling some of the most relevant chapters of philosophy of science. The focus is put onto the roles of disciplines and their scholars involved in interdisciplinary contexts in order to further motivate as well as to hint at a number of catalysing forces and fruitful impacts of outside |
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2. |
Record Nr. |
UNINA9910863189903321 |
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Autore |
Yoon Hyung |
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Titolo |
Palladium and Nickel Catalyzed Transformations Forming Functionalized Heterocycles / / by Hyung Yoon |
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Pubbl/distr/stampa |
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Springer International Publishing, 2020 |
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Cham : , : Springer International Publishing : , : Imprint : Springer, , 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 (XXIX, 212 p. 552 illus., 35 illus. in color.) |
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Collana |
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Springer Theses, Recognizing Outstanding Ph.D. Research, , 2190-5053 |
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Disciplina |
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Soggetti |
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Catalysis |
Chemistry, Inorganic |
Chemistry, Organic |
Organometallic chemistry |
Chemistry, Physical and theoretical |
Inorganic Chemistry |
Organic Chemistry |
Organometallic Chemistry |
Physical Chemistry |
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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 contenuto |
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Chapter 1. Carbohalogenation Catalyzed by Palladium and Nickel -- Chapter 2. Diastereoselective Pd-Catalyzed Aryl Cyanation and Aryl Borylation -- Chapter 3. Pd-Catalyzed Spirocyclization via C–H Activation and Benzyne/Alkyne Insertion. |
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Sommario/riassunto |
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This book presents Pd- and Ni-catalyzed transformations generating functionalized heterocycles. Transition metal catalysis is at the forefront of synthetic organic chemistry since it offers new and powerful methods to forge carbon–carbon bonds in high atom- and step-economy. In Chapter 1, the author describes a Pd- and Ni- |
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catalyzed cycloisomerization of aryl iodides to alkyl iodides, known as carboiodination. In the context of the Pd-catalyzed variant, the chapter explores the production of enantioenriched carboxamides through diastereoselective Pd-catalyzed carboiodination. It then discusses Ni-catalyzed reactions to generate oxindoles and an enantioselective variant employing a dual ligand system. Chapter 2 introduces readers to a Pd-catalyzed diastereoselective anion-capture cascade. It also examines diastereoselective Pd-catalyzed aryl cyanation to synthesize alkyl nitriles, a method that generates high yields of borylated chromans as a single diastereomer, and highlights its synthetic utility. Lastly, Chapter 3 presents a Pd-catalyzed domino process harnessing carbopalladation, C–H activation and π-system insertion (benzynes and alkynes) to generate spirocycles. It also describes the mechanistic studies performed on these reactions. |
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