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Author: Alan Hutchinson
Publisher:
ISBN:
Category : Metabolites
Languages : en
Pages : 264
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Book Description
Author: Alan Hutchinson
Publisher:
ISBN:
Category : Metabolites
Languages : en
Pages : 264
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Book Description
Author: Elias J. Corey
Publisher: Elsevier
ISBN: 0128001518
Category : Science
Languages : en
Pages : 334
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Book Description
Written by world-renowned and best-selling experts, Nobel Laureate E. J. Corey and Laszlo Kurti, Enantioselective Chemical Synthesis offers an authoritative and comprehensive overview of the field's progress; the processes and tools for key formations; future development for complex, stereocontrolled (enantiomeric or diastereoisomeric) molecules; and valuable examples of multi-step syntheses. Utilizing a color-coded scheme to illustrate chemical transformations, Enantioselective Chemical Synthesis provides clear explanation and guidance through vital asymmetrical syntheses and insight into the next steps for the field. Researchers, professionals, and academics will benefit from this valuable, thorough, and unique resource. - In Part I, the authors present clearly, comprehensively and concisely the most useful enantioselective processes available to synthetic chemists. - Part II provides an extensive discussion of the most logical ways to apply these new enantioselective methods to the planning of syntheses of stereochemically complex molecules. This hitherto neglected area is essential for the advancement of enantioselective synthesis to a more rational and powerful level. - Part III describes in detail many reaction sequences which have been used successfully for the construction of a wide variety of complex target molecules - Clearly explains stereochemical synthesis in theory and practice - Provides a handy tool box for scientists wishing to understand and apply chiral chemical synthesis - Describes almost 50 real life examples of asymmetric synthesis in practice and examines how the chiral centers were introduced at key synthetic stages
Author: José Pérez Sestelo
Publisher: MDPI
ISBN: 3039435671
Category : Science
Languages : en
Pages : 234
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Book Description
In this Special Issue, recent advances in cross-coupling reactions are presented in the form of original research articles, reviews, and short communications. These contributions cover different topics in this area, including novel coupling reactions, reaction conditions, synthetic alternatives, metal ligands, and applications for new pharmaceutical compounds and organic materials. In particular, the reviews deal with methodologies such as the synthesis of diarylketones through palladium catalysis and the most relevant examples of Suzuki–Miyaura and Buchwald–Hartwig coupling reactions in the synthesis of bioactive compounds. The synthetic utility of cross-coupling reactions for the synthesis of medium-size rings and the utility of Stille and Suzuki coupling reactions for the synthesis of new molecular machines based on sterically hindered anthracenyl trypticenyl units are also summarized. The original research articles present the synthesis of 2-alkynylpyrrols by inverse Sonogashira coupling and the synthesis of indoles under oxidative dearomative cross-dehydrogenative conditions. The efficient combination of iridium-catalyzed C–H borylation of aryl halides with the Sonogashira coupling and a sequential iridium-catalyzed borylation of NH-free pyrroles followed by a Suzuki–Miyaura reaction are included. The synthesis of aryl propionic acids, a common structural motif in medicinal chemistry, and the synthesis of new organic dyes are also covered.
Author: Maliha Uroos
Publisher: Elsevier
ISBN: 0323972489
Category : Science
Languages : en
Pages : 236
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Book Description
Indole Alkaloids: Spirooxindole details the multistep synthesis of natural products using schematic diagrams, providing a quick-and-easy way to review and understand new and novel synthetic strategies to construct structural frameworks of natural products. As a volume in the Visual Guides to Natural Product Synthesis series, this book presents the schematic total syntheses of natural products containing a "spirooxindole core structure. It covers spirooxindole molecules through visual diagrams, highlighting key steps involved in total, formal and semi-syntheses. Sections cover Brevianamide A and B, Citrinadin A and B, Coerulescine and Horsfiline, Elacomine and Isoelacomine, Gelsemine, Paraherquamide A and B, Rynchophylline, Isorynchophylline, and more. Visual layouts provide quick-and- easy access to developed synthetic routes towards the targeted spirooxindoles. - Outlines synthetic strategies for natural products bearing a spirooxindole core structure - Includes schematic diagrams of multistep synthetic routes, highlighting key steps along the way - Describes all routes for the formal synthesis, semi-synthesis and total synthesis of spirooxindole alkaloids
Author: Anthony Wayne McCollum
Publisher:
ISBN:
Category : Diterpenes
Languages : en
Pages : 200
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Book Description
![I. Completion of the Synthesis of Kopsia Lapidilecta Alkaloid (±)-lapidilectine B. ; II. Synthesis of 1-azabicyclo[n.3.0]alkanes Via [3+2] Cycloadditions of Nonstabilized Azomethine Ylides PDF](https://books.google.com/books/content/images/frontcover/2P4dAQAAMAAJ?fife=w80-h100)
Author: Patrick Stoy
Publisher:
ISBN:
Category :
Languages : en
Pages : 816
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Book Description
Author: Robert A. Volkmann
Publisher:
ISBN:
Category :
Languages : en
Pages : 228
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Book Description
Author:
Publisher:
ISBN:
Category : Dissertations, Academic
Languages : en
Pages : 714
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Book Description
Author: ROGER CLAYTON KIERSTEAD
Publisher:
ISBN:
Category :
Languages : en
Pages : 220
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Book Description
Author: Carolyn Burger Abrahams
Publisher:
ISBN:
Category : Acids
Languages : en
Pages : 182
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Book Description
