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Index of Named Reactions

Although the index of named reactions in Eicher-Hauptmann s excellent book includes this reaction as Balaban reaction, the more appropriate name should be that adopted in the present review and included also in the Hassner-Stumer book. ... [Pg.402]

The Index of Named Reactions covers the named reactions, reaction types and principles for synthesis of the aforementioned heterocyclic systems. The heterocycle resulting from a named synthesis is shown in brackets, e.g. Fischer synthesis (indole). [Pg.621]

Chapter 9 consists of a series of problems - presented in broad variety and selected almost exclusively from the most recent Hterature - and is intended to deepen the knowledge and understanding of the reader and to extend the topics of heterocycHc chemistry treated in this book. The concluding chapters contain the General Subject Index (10.1) and an Index of Named Reactions (10.2). [Pg.643]

Wheeler and Gowan, Name Index of Organic Reactions, 1953 (Society of Chemical Industry). [Pg.1130]

The Merck Index, Merck CO., Inc., Whitehouse Station, N. J. (now in the 13th Edition) Each edition has an updated list of Named Reactions. [Pg.1]

For rapid access to information such as mp, bp, density, solubility, optical rotation, A max, and crystal form, one turns first to the Handbook of Chemistry and Physics where information is found on some 15,000 organic compounds, including the Beilstein reference to each compound. These compounds are well known and completely characterized. The majority are commercially available. The Merck Index contains information on nearly 10,000 compounds, especially those of pharmaceutical interest. In addition to the usual physical properties, information and literature references to synthesis, isolation, and medicinal properties, such as toxicity data, are found. The last third of the book is devoted to such items as a long cross index of names (which is very useful for looking up drugs), a table of organic name reactions, an excellent section on first aid for poisons, a list of chemical poisons, and a listing of the locations of many poison control centers. [Pg.623]

The print edition of this Reference Work contains two indexes, the Index of Drug Names and the Index of Adverse Reactions . Both indexes are print oriented and point at pages in the main text in which a reaction is discussed or a drug name used. [Pg.1]

Two other sites related to chemical synthesis inclnde http //orgchem.chem.nconn.edn/namereact/named.html which inclndes details of abont 100 named reactions and the reaction index at http //www.pmf.nkim.edu.mk/PMF/ Chemistry/reactions/rindex.htm, which contains a very extensive list of named reactions in organic chemistry. [Pg.264]

J.E. Gowan and T.S. Weeler, Name Index of Organic Reaction, Longmans, London, 1960. [Pg.506]

Name reactions are also defined in two other publications. Name Reactions in Organic Chemistry by A. R. Surrey (Academic Press, 1961) describes about 125 reactions known by the name of their discoverers listed in alphabetical order and gives for each a brief biography, a description of the reaction and its mechanism together with an indication of its usefulness and limitations, and a literature reference. Name Index of Organic Reactions by J. E. Gowan and T. S. Wheeler (Interscience, 1960) gives concise explanations with references of 739 named reactions. Many... [Pg.147]

It is a great honor to write a foreword to the preeminent dictionary of named processes in the chemical industry. Named industrial processes have always been the poor relation of named reactions. On my bookshelf, I have several books devoted to named organic reactions, including ones by J. S. Gowan and T. S. Wheeler (1960), Alexander Surrey (2nd ed., 1961), and R. C. Denny (1969). The Merck Index also has an excellent section on named reactions. For industrial processes, Comyns stands practically alone, its only rival being the book by Kurt Wagner (1951), which has a much broader brief and is now completely out of date. Yet industrial processes and names are more often mentioned than named organic reactions and far more often by nonchemists. The Haber-Bosch process is far better known than the Cannizzaro reaction or the Michael addition. [Pg.409]

Secondly, chemical IR may be thought of as a specialized index into the scientific and patent literature, with the chemical structure representing an extremely condensed abstract of the journal article or patent document. In this sense, the structures are not stored for their intrinsic interest, but as pointers to other documents, some of which, for example, may be related to their synthesis, physicochemical properties and numeric data, or applications. This is the sense in which a few data vendors supply chemical and reaction databases (Derwent and Institute for Scientific Information), and the alternate sense in which the CAS databases may be used. The use of CIR systems in synthesis design - providing access, for example, to databases of reagents or starting materials, or of name reactions - provides a crucial tool for the contemporary chemical and pharmaceutical industry. [Pg.2772]

This index contains over 40,000 individual entries to the 6200 text pages of Volumes 1-7. The index mainly covers general classes of heterocyclic compound and specific heterocyclic compounds, but also included are natural products, other organic and organometallic compounds where their synthesis or use involves heterocyclic compounds, types of reaction, named reactions, spectroscopic techniques and topics involving heterocyclic compounds. [Pg.507]

The Subject Index of over 20 000 entries has been compiled from keywords, names and formulae in the text and tables. It covers general classes of compound, specific compounds, general types of reaction, specific and named reactions, spectral and other properties, and other topics in heterocyclic chemistry. More details are again given at the beginning of the index in Volume 8. [Pg.6]

The choice of which reactions to include is not an easy one. First there are the well known "Name Reactions", that have appeared in various monographs or in the old Merck index. Some of these are so obvious mechanistically to the modern organic chemistry practitioner that we have in fact omitted them for instance esterification of alcohols with acid chlorides - the Schotten-Baumann procedure. Others are so important and so well entrenched by name, like the Baeyer-Villiger ketone oxidation, that it is impossible to ignore them. In general we have kept older name reactions that are not obvious at first glance. [Pg.459]

The third edition contains major improvements over the previous two editions. I have updated references. Each reaction is now supplemented with two to three representative examples in synthesis to showcase its synthetic utility. As Emil Fischer stated Science is not an abstraction but as a product of human endeavor it is inseparably bound up in its development with the personalities and fortunes of those who dedicate themselves to it. To that end, I added biographical sketches for most of the chemists who discovered or developed those name reactions. Furthemore, I have significantly beefed up the subject index to help the reader navigate the book more easily. [Pg.660]

Three main parameters were used to evaluate the efficiency of the polymerization, namely monomer conversion (Cmma), initiation efficiency of the reaction (/ = Mn theo/3 n,SEc), and polydispcrsity index (PDI). These results are depicted in Fig. 2. It is obvious that the Cu(I)-catalyzed systems are more effective than the Fe(II)-catalyzed systems under the studied conditions. It was concluded that a bipyridine based ligand with a critical length of the substituted alkyl group (e.g., dHbpy) shows the best performance in Cu(I)-mediated systems. Besides, Cu(I) halide-mediated ATRP with 4,5 -Mbpy as the ligand and TsCl as the initiator was better controlled than that with dMbpy as the ligand, and polymers with much lower PDI values were obtained in the former case. [Pg.24]


See other pages where Index of Named Reactions is mentioned: [Pg.557]    [Pg.630]    [Pg.557]    [Pg.630]    [Pg.1211]    [Pg.382]    [Pg.10]    [Pg.288]    [Pg.418]    [Pg.10]    [Pg.27]    [Pg.472]    [Pg.55]    [Pg.1618]    [Pg.1628]    [Pg.1342]    [Pg.772]    [Pg.503]    [Pg.628]    [Pg.31]    [Pg.1251]   


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