Inicio > Matemáticas y ciencia > Química > Química orgánica > Stereoselective Synthesis in Organic Chemistry
Stereoselective Synthesis in Organic Chemistry

Stereoselective Synthesis in Organic Chemistry

Atta-ur-Rahman / Zahir Shah

132,74 €
IVA incluido
Disponible
Editorial:
Springer Nature B.V.
Año de edición:
2011
Materia
Química orgánica
ISBN:
9781461383291
132,74 €
IVA incluido
Disponible

Selecciona una librería:

  • Librería Samer Atenea
  • Librería Aciertas (Toledo)
  • Kálamo Books
  • Librería Perelló (Valencia)
  • Librería Elías (Asturias)
  • Donde los libros
  • Librería Kolima (Madrid)
  • Librería Proteo (Málaga)

This monumental tome by Prof. Atta-ur-Rahman and Dr. Zahir Shah pres­ ents a broad overall perspective of stereo selectivity in the synthesis of or­ ganic molecules. Thus it treats a problem that is of fundamental importance and will be even more important in the future as the drug industry is required to supply 1000/0 optically pure compounds. After an exposition of general principles, the following subjects are treated: Catalytic Reductions, Heterogeneous Catalytic Hydrogenations, Stereoselective Non-Catalytic Reductions, Stereos elective Carbon-Carbon Bond Forming Reactions, Asymmetric Oxidations, Asymmetric Carbon­ Heteroatom Bond Formations, Enzyme Catalyzed Reactions, Stereo­ selective Free Radical Reactions, and finally Miscellaneous Stereoselective Reactions. For each subject, a wealth of examples are given. The highly selective reactions are mentioned along with reactions that are not. This is helpful as it will teach the practical chemist what to avoid. Much progress has been made in the last two decades in the design of new, very stereoselective reactions which can be applied in industry. For example, and in alphabetical order, we can mention (among other peers): H.C. Brown (hydroboration), D.C. Evans (carbon-carbon bond forma­ tion), R. Noyori (BINAP reagents for hydrogenation), and K.B. Sharpless (epoxidation and dihydroxylation of double bonds). Thus the field has completely changed since the 1950s, when optically pure compounds were always obtained by difficult resolutions of racemates and not by stereoselec­ tive reactions.

Artículos relacionados

  • Organic Chemistry Problems and Solutions
    G.R. Vijayagopal / V. Raman K.
    In the competitive world of entrance examinations for premier engineering and medical institutions, mastering the art of problem-solving is crucial. This book serves as a beacon for students aiming to secure their places in prestigious institutions such as IITs, CSIR laboratories, IISc, and top medical colleges through examinations like IIT-JEE, AIEEE, JIPMER, JAM, CSIR, NET, G...
    Disponible

    46,17 €

  • CHEMISTRY OF NATURAL PRODUCTS
    K. Anand Solomon
    'Chemistry of Natural Products' opens a window to the profound impact that natural products, derived from both plant and animal origins, have on human life. This book is meticulously crafted to illuminate the fascinating journey from the isolation and characterization of these natural compounds to understanding their biological and pharmacological activities. Aimed at students ...
    Disponible

    23,96 €

  • QUALITATIVE AND QUANTITATIVE ANALYSIS OF PHYTOCHEMICALS
    Mital Soni / Vijay Ram
    Kachchh district’s unique geographic features, situated near the Tropic of Cancer and encompassing one of Gujarat’s Gulfs, result in diverse environmental conditions throughout the year. The region, predominantly rural, is rich in traditional plant-based folk medicine, reflecting its high biodiversity and ecological value. Understanding the therapeutic potential of medicinal pl...
    Disponible

    54,25 €

  • The Emergence of Life
    Pier Luigi Luisi
    ...
  • Understanding Organic Reaction Mechanisms
    Adam Jacobs
    ...
    Disponible

    147,51 €

  • Synthese von (-) -Pyrenophorol, Bewertung von Heterozyklen gegen Krebs
    PERUGU EDUKONDALU
    Die Totalsynthese von (-)-Pyrenophorol mit hoher Enantioselektivität wurde durchgeführt, wobei die Stereozentren durch hydrolytische kinetische Jacobsen-Auflösung und asymmetrische Sharpless-Dihydroxylierung etabliert wurden und die Zyklisierung durch intermolekulare Mitsunobu-Zyklisierung erreicht wurde. Die Verbindung 90b mit der elektronenspendenden 3,4,5-Trimethoxygruppe am...
    Disponible

    84,90 €