By Gattermann L.
Der Anfänger findet hier eine ausführliche Einführung in den Umgang mit den Laborgeräten des organisch-chemischen Praktikums. Außerdem werden nützliche Informationen z.B. zur Herstellung von Lösungen bestimmter Konzentrationen oder zum Reinigen und Trocknen von Lösungsmitteln angeboten.
By Raymond Chang, Jason Overby
The 6th version of basic Chemistry: The Essential
Concepts, keeps the culture of providing purely the
material that's necessary to a one-year common chemistry
course. As with past variants, it comprises the entire core
topics which are important for a great beginning in general
chemistry with out sacrifi cing intensity, readability, or rigor.
General Chemistry covers those subject matters within the comparable depth
and on the related point as 1100-page texts. All crucial topics
are within the textual content except for descriptive chemistry.
Therefore, this ebook isn't a condensed model of a giant text.
Our wish is this concise-but-thorough procedure will
appeal to effi ciency-minded teachers and may please
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over the years exhibits that there's a powerful want for such a
text. So now we have written a textual content containing the entire center concepts
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By S. Uebel, K. H. Wiesmüller, G. Jung, R. Tampé (auth.), Professor Dr. Michael Famulok, Professor Dr. Ernst-L. Winnacker, Professor Dr. Chi-Huey Wong (eds.)
The essence of combinatorial chemistry or suggestions concerning "molecular variety" is to generate huge, immense populations of molecules and to take advantage of acceptable screening strategies to isolate energetic parts contained in those libraries. this concept has been the point of interest of study either in academia and within the pharmaceutical or biotechnology undefined. Its advancements cross hand in hand with an exploding variety of power drug goals rising from genomics and proteomics study. whilst the editors of present themes in Microbiology and Immunology inspired us to gather the current quantity on Combinatorial Chemistry in Biology, we instantly felt that this could end up really valuable for the viewers of this sequence. the sector of combinatorial chemistry extends over a vast diversity of disciplines, from artificial natural chemistry to biochemistry, from fabric sciences to mobilephone biology. every one of those fields can have its personal view in this subject, anything that's mirrored in more and more monographs and "special variants" of jour nals dedicated to this factor or facets thereof. The identify of the current quantity of Springer-Verlag's sequence means that it additionally has its personal certain concentration. And, normally talking, this isn't improper: we might even declare the exact concentration of this quantity is at the immunologically correct features of combinatorial chemistry.
By M. Kaloustian
Within the final region century there were merely seminal contributions within the box of natural stereochemistry - either via Kurt Mislow and his coworkers - ones that experience clarified the elemental thoughts of stereotopicity and chirotopicity. no longer withstanding a number of different sporadic contributions by means of others, thus far there were no systematic makes an attempt to unify and advance the conceptual framework and terminology of natural stereochemistry. current phrases are often misused or abused, wanted phrases - redundant, complicated or debatable - are invented randomly, and but different wanted phrases haven't noticeable the sunshine of day. This three-part paintings offers the weather of an easy, uniform and finished language of the stereochemical underpinnings of natural chemistry. it truly is crucial analyzing for business chemists, graduate scholars, collage professors and business researchers within the box of natural Stereochemistry.
"Covers worldwide and family pageant, advertising techniques, working bills, and environmental and safeguard laws for chemical pros in any respect degrees. includes up to date mergers and acquisitions of chemical companies."
By G E Inglett; S Ingemar Falkehag; American Chemical Society
By Caprio V., Williams J.
Content material: Preface to the second one variation. Preface to the 1st variation. 1 creation. 1.1 Reactions Amenable to uneven Catalysis. 1.2 task of (R) and (S) Stereochemical Descriptors. Futher studying. References. 2 relief of Alkenes. 2.1 uneven Hydrogenation with Rhodium Complexes. 2.2 uneven Hydrogenation with Ruthenium Catalysts. 2.3 Alkene Hydrogenation with Titanium and Zirconium Catalysts. 2.4 Alkene Hydrogenation with Iridium Catalysts. 2.5 Alkene Hydrogenation with Organocatalysts. 2.6 Alkene Hydrosilylation. 2.7 Alkene Hydroboration. 2.8 Hydroamination. 2.9 Hydroformylation. 2.10 Hydroacylation of Alkenes. 2.11 Hydrocyanation of Alkenes. References. three aid of Ketones and Imines. 3.1 Hydrogenation of Ketones. 3.2 Hydrogenation and move Hydrogenation of Imines and comparable Compounds. 3.3 move Hydrogenation of Ketones. 3.4 Heterogeneous Hydrogenation. 3.5 relief of Ketones utilizing Enantioselective Borohydride Reagents. 3.6 Hydrosilylation of Ketones. 3.7 Hydrosilylation of Imines and Nitrones. References. four Epoxidation. 4.1 Epoxidation of Allylic Alcohols. 4.2 Epoxidation with Metal(salen) Complexes. 4.3 Epoxidation utilizing Metal-Porphyrin-Based Catalysts. 4.4 OtherMetal-Catalysed Epoxidations of Unfunctionalised Olefins. 4.5 Epoxidation of Electron-Deficient Alkenes. 4.6 Epoxidation with Iminium Salts. 4.7 Epoxidation with Ketone Catalysts. 4.8 Epoxidation of Aldehydes. 4.9 Aziridination of Alkenes. 4.10 Aziridination of Imines. References. five extra Oxidation Reactions. 5.1 Dihydroxylation. 5.2 Aminohydroxylation. 5.3 alpha-Heterofunctionalisation of Aldehydes and Ketones. 5.4 Oxidation of C-H. 5.5 Baeyer-Villiger Oxidation. 5.6 Oxidation of Sulfides. References. 6 Nucleophilic Addition to Carbonyl Compounds. 6.1 Addition of Organozincs to Carbonyl Compounds. 6.2 Addition of Cyanide to Aldehydes and Ketones. 6.3 Allylation of Aldehydes. 6.4 Hydrophosphonylation of Aldehydes. 6.5 Nucleophilic Additions to Imines. References. 7 The Aldol and comparable Reactions. 7.1 The Aldol response. 7.2 Isocyanide and comparable Aldol Reactions. 7.3 The Nitroaldol response. 7.4 Addition of Enolates to Imines. 7.5 Darzens Condensation. 7.6 Morita-Baylis-Hillman response. 7.7 Carbonyl-Ene Reactions. References. eight Cycloadditions. 8.1 Diels-Alder Reactions. 8.2 Inverse Electron call for Diels-Alder Reactions. 8.3 Hetero-Diels-Alder Reactions. 8.4 1,3-Dipolar Cycloaddition Reactions. 8.5 [2+2] Cycloadditions. 8.6 Pauson-Khand-Type Reactions. References. nine Catalytic Reactions related to Carbenes and Ylides. 9.1 Cyclopropanation. 9.2 Insertion Reactions. 9.3 uneven Ylide Reactions. References. 10 Catalytic Carbon-Carbon Bond-Forming Reactions. 10.1 Cross-Coupling Reactions. 10.2 Metal-Catalysed Allylic Substitution. 10.3 Heck Reactions. 10.4 Alkylmetalation of Alkenes. References. eleven Conjugate Addition Reactions. 11.1 Conjugate Addition of Enolates. 11.2 Conjugate Addition of Sulfur Nucleophiles. 11.3 Conjugate Addition of Nonstabilised Nucleophiles. 11.4 Conjugate Addition with Nitrogen-Based Nucleophiles and Electrophiles. References. 12 additional Catalytic Reactions. 12.1 Isomerisations and Rearrangements. 12.2 Deprotonation Reactions. 12.3 Protonation Reactions. 12.4 Alkylation and Allylation of Enolates. 12.5 Formation of Alkenes. 12.6 Oxyselenylation-Elimination Reactions. 12.7 The Benzoin Condensation. 12.8 Ester Formation and Hydrolysis. 12.9 Ring-Opening of Epoxides. References. Index