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Organic synthesis /

A reactions oriented course is a staple of most graduate organic programs, and synthesis is taught either as a part of that course or as a special topic. Ideally, the incoming student is an organic major, who has a good working knowledge of basic reactions, stereochemistry and conformational princip...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Smith, Michael, 1946 October 17-
Formato: Electrónico eBook
Idioma:Inglés
Publicado: [Irvine, CA] : Wavefunction, Inc., [2010]
Edición:3rd ed.
Temas:
Acceso en línea:Texto completo

MARC

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100 1 |a Smith, Michael,  |d 1946 October 17- 
245 1 0 |a Organic synthesis /  |c Michael B. Smith. 
250 |a 3rd ed. 
260 |a [Irvine, CA] :  |b Wavefunction, Inc.,  |c [2010] 
300 |a 1 online resource (xxvii, 1506 pages) :  |b illustrations 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
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520 |a A reactions oriented course is a staple of most graduate organic programs, and synthesis is taught either as a part of that course or as a special topic. Ideally, the incoming student is an organic major, who has a good working knowledge of basic reactions, stereochemistry and conformational principles. In fact, however, many (often most) of the students in a first year graduate level organic course have deficiencies in their undergraduate work, are not organic majors and are not synthetically inclined. To save students much time catching up this text provides a reliable and readily available source for background material that will enable all graduate students to reach the same high level of proficiency in organic chemistry. Produced over many years with extensive feedback from students taking an organic chemistry course this book provides a reaction based approach. The first two chapters provide an introduction to functional groups; these are followed by chapters reviewing basic organic transformations (e.g. oxidation, reduction). The book then looks at carbon-carbon bond formation reactions and ways to 'disconnect' a bigger molecule into simpler building blocks. Most chapters include an extensive list of questions to test the reader's understanding. There is also a new chapter outlining full retrosynthetic analyses of complex molecules which highlights common problems made by scientists. The book is intended for graduate and postgraduate students, scientific researchers in chemistry New publisher, new edition; extensively updated and corrected Over 950 new references with more than 6100 references in total Over 600 new reactions and figures replaced or updated Over 300 new homework problems from the current literature to provide nearly 800 problems to test reader understanding of the key principles Free molecular modeling software to explore 60 new synthesis-oriented molecular modeling problems; designed to aid visualisation and understanding of organic synthesis. 
504 |a Includes bibliographical references and index. 
505 0 |a Retrosynthesis, stereochemistry, and conformations -- Acids, bases and functional group exchange reactions -- Oxidation -- Reduction -- Hydroboration -- Stereocontrol and ring formation -- Protecting groups -- Cd disconnect products: nucleophilic species that form carbon-carbon bonds -- Cd disconnect products: nucleophilic species that form carbon-carbon bonds: enolate anions -- Synthetic strategies -- Pericyclic carbon-carbon bond forming reactions: multiple bond disconnections -- Ca disconnect products: electrophilic carbon-carbon bond forming reactions -- Carbon radical disconnect products: formation of carbon-carbon bonds via radicals and carbenes -- Student synthesis: the first synthetic problem. 
588 0 |a Print version record. 
650 0 |a Organic compounds  |x Synthesis. 
650 6 |a Compos�es organiques  |x Synth�ese.  |0 (CaQQLa)201-0020323 
650 7 |a Organic compounds  |x Synthesis  |2 fast  |0 (OCoLC)fst01047668 
776 0 8 |i Print version:  |a Smith, Michael, 1946 October 17-  |t Organic synthesis.  |b 3rd ed.  |d [Irvine, CA]: Wavefunction, Inc., [2010]  |z 1890661406  |w (OCoLC)671303987 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9781890661403  |z Texto completo