Organic chemistry /

Detalles Bibliográficos
Autor principal: Clayden, Jonathan
Otros Autores: Greeves, Nick, Warren, Stuart, Wothers, Peter
Formato: Libro
Lenguaje:Inglés
Publicado: [Oxford] : Oxford University Press, c2001
Edición:1st. ed.
Materias:
Aporte de:Registro referencial: Solicitar el recurso aquí
LEADER 03723cam a22009137a 4500
001 BIBLO-39196
003 AR-BaUEN
005 20241226171838.0
008 080424s2009 xxkad||f |||| 001 0|eng|d
020 |a 9780198503460 
040 |a AR-BaUEN  |b spa  |c AR-BaUEN 
044 |a xxk 
080 |a 547 
100 1 |a Clayden, Jonathan 
245 1 0 |a Organic chemistry /   |c Jonathan Cayden ... [et al.] 
250 |a 1st. ed. 
260 |a [Oxford] :   |b Oxford University Press,  |c c2001 
300 |a 1512 p. :  |b gráfs., il. 
500 |a Incluye problemas y ejercicios al final de cada capítulo. 
504 |a Índice analítico de materias. 
505 0 0 |g 1  |t What is organic chemistry 
505 0 0 |g 2  |t Organic structures 
505 0 0 |g 3  |t Determining organic structures 
505 0 0 |g 4  |t Structures of molecules 
505 0 0 |g 5  |t Organic reactions 
505 0 0 |g 6  |t Nucleophilic addition to the carbonyl group 
505 0 0 |g 7  |t Delocalization and conjugation 
505 0 0 |g 8  |t Acidity, basicity, and pKa 
505 0 0 |g 9  |t Using organometallic reagents to make C-C bonds 
505 0 0 |g 10  |t Conjugate addition 
505 0 0 |g 11  |t Proton nuclear magnetic resonance 
505 0 0 |g 12  |t Nucleophilic substitution at the carbonyl (C=O) group 
505 0 0 |g 13  |t Equilibria, rates, and mechanisms: summary of mechanistic principles 
505 0 0 |g 14  |t Nucleophilic substitution at C=O with loss of carbonyl oxygen 
505 0 0 |g 15  |t Review of spectroscopic methods 
505 0 0 |g 16  |t Stereochemistry 
505 0 0 |g 17  |t Nucleophilic substitution at saturated carbon 
505 0 0 |g 18  |t Conformational analysis 
505 0 0 |g 19  |t Elimination reactions 
505 0 0 |g 20  |t Electrophilic addition to alkenes 
505 0 0 |g 21  |t Formation and reactions of enols and enolates 
505 0 0 |g 22  |t Electrophilic aromatic substitution 
505 0 0 |g 23  |t Electrophilic alkenes 
505 0 0 |g 24  |t Chemoselectivity: selective reactions and protection 
505 0 0 |g 25  |t Synthesis in action 
505 0 0 |g 26  |t Alkylation of enolates 
505 0 0 |g 27  |t Reactions of enolates with aldehydes and ketones: the aldol reaction 
505 0 0 |g 28  |t Acylation at carbon 
505 0 0 |g 29  |t Conjugate addition of enolates 
505 0 0 |g 30  |t Retrosynthetic analysis 
505 0 0 |g 31  |t Controlling the geometry of double bonds 
505 0 0 |g 32  |t Determination of stereochemistry by spectroscopic methods 
505 0 0 |g 33  |t Stereoselective reactions of cyclic compounds 
505 0 0 |g 34  |t Diastereoselectivity 
505 0 0 |g 35  |t Pericyclic reactions 1: cycloadditions 
505 0 0 |g 36  |t Pericyclic reactions 2: sigmatropic and electrocyclic reactions 
505 0 0 |g 37  |t Rearrangements 
505 0 0 |g 38  |t Fragmentation 
505 0 0 |g 39  |t Radical reactions 
505 0 0 |g 40  |t Synthesis and reactions of carbenes 
505 0 0 |g 41  |t Determining reaction mechanisms 
505 0 0 |g 42  |t Saturated heterocycles and stereoelectronics 
505 0 0 |g 43  |t Aromatic heterocycles 1: structures and reactions 
505 0 0 |g 44  |t Aromatic heterocycles 2: synthesis 
505 0 0 |g 45  |t Asymmetric synthesis 
505 0 0 |g 46  |t Organo-main-group chemistry I: sulfur 
505 0 0 |g 47  |t Organo-main-group chemistry II: boron, silicon, and tin 
505 0 0 |g 48  |t Organometallic chemistry 
505 0 0 |g 49  |t The chemistry of life 
505 0 0 |g 50  |t Mechanisms in biological chemistry 
505 0 0 |g 51  |t Natural products 
505 0 0 |g 52  |t Polymerization 
505 0 0 |g 53  |t Organic chemistry today 
650 1 7 |2 spines  |a QUIMICA ORGANICA 
700 1 |a Greeves, Nick 
700 1 |a Warren, Stuart 
700 1 |a Wothers, Peter 
931 |a DQO 
962 |a info:eu-repo/semantics/book  |a info:ar-repo/semantics/libro  |b info:eu-repo/semantics/publishedVersion