New Gold-Catalyzed Reactions and Applications for the Synthesis of Alkaloids

Nonfiction, Science & Nature, Science, Chemistry, Technical & Industrial, Organic
Cover of the book New Gold-Catalyzed Reactions and Applications for the Synthesis of Alkaloids by Ana Escribano Cuesta, Springer International Publishing
View on Amazon View on AbeBooks View on Kobo View on B.Depository View on eBay View on Walmart
Author: Ana Escribano Cuesta ISBN: 9783319007021
Publisher: Springer International Publishing Publication: August 13, 2013
Imprint: Springer Language: English
Author: Ana Escribano Cuesta
ISBN: 9783319007021
Publisher: Springer International Publishing
Publication: August 13, 2013
Imprint: Springer
Language: English

Ana Escribano Cuesta's thesis presents a detailed study of the inter- and intramolecular reactions of carbonyl compounds with 1,6-enynes using gold (I) complexes. An important part of the work involved streamlining the variables that allow the selective synthesis of different products such as tricyclic compounds, dihydropyrans, 1,3-dienes or cyclobutenes. The second chapter highlights the importance and difficulties in synthesising a cyclobutene subunit and the author includes a detailed description of how the products were prepared. The final chapter outlines the synthesis of lundurines using methodology developed by the author's research group for intramolecular gold-catalyzed cyclization of indoles with alkynes. The lundurine products developed in this work show significant in vitro cytoxicity toward B16 melanoma cells. The work in this thesis has led to a number of publications in high-profile chemistry journals.

View on Amazon View on AbeBooks View on Kobo View on B.Depository View on eBay View on Walmart

Ana Escribano Cuesta's thesis presents a detailed study of the inter- and intramolecular reactions of carbonyl compounds with 1,6-enynes using gold (I) complexes. An important part of the work involved streamlining the variables that allow the selective synthesis of different products such as tricyclic compounds, dihydropyrans, 1,3-dienes or cyclobutenes. The second chapter highlights the importance and difficulties in synthesising a cyclobutene subunit and the author includes a detailed description of how the products were prepared. The final chapter outlines the synthesis of lundurines using methodology developed by the author's research group for intramolecular gold-catalyzed cyclization of indoles with alkynes. The lundurine products developed in this work show significant in vitro cytoxicity toward B16 melanoma cells. The work in this thesis has led to a number of publications in high-profile chemistry journals.

More books from Springer International Publishing

Cover of the book Assessment of Learning Outcomes in Higher Education by Ana Escribano Cuesta
Cover of the book Grand Strategies of Weak States and Great Powers by Ana Escribano Cuesta
Cover of the book INCREaSE by Ana Escribano Cuesta
Cover of the book Space Capitalism by Ana Escribano Cuesta
Cover of the book Improving Energy Decisions by Ana Escribano Cuesta
Cover of the book Deconstructing Ethnography by Ana Escribano Cuesta
Cover of the book Connective Tissue Disease by Ana Escribano Cuesta
Cover of the book New Trends in Applied Harmonic Analysis by Ana Escribano Cuesta
Cover of the book The Nexus: Energy, Environment and Climate Change by Ana Escribano Cuesta
Cover of the book Clinical Cases in Psoriasis by Ana Escribano Cuesta
Cover of the book Twin Peaks for Europe: State-of-the-Art Financial Supervisory Consolidation by Ana Escribano Cuesta
Cover of the book Algorithmic Advances in Riemannian Geometry and Applications by Ana Escribano Cuesta
Cover of the book Quantifying Interactions of Biomolecules with Inorganic Surfaces by Ana Escribano Cuesta
Cover of the book Modeling and Control of Greenhouse Crop Growth by Ana Escribano Cuesta
Cover of the book Advances in Web-Based Learning – ICWL 2018 by Ana Escribano Cuesta
We use our own "cookies" and third party cookies to improve services and to see statistical information. By using this website, you agree to our Privacy Policy