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Stereochemistry : a three-dimensional insight /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Karnik, Anil V.
Otros Autores: Hasan, Mohammed
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Amsterdam : Elsevier, 2021.
Temas:
Acceso en línea:Texto completo

MARC

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003 OCoLC
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008 210725s2021 ne o 001 0 eng d
040 |a YDX  |b eng  |e pn  |c YDX  |d OPELS  |d OCLCO  |d EBLCP  |d OCLCF  |d UKMGB  |d N$T  |d UKAHL  |d OCLCO  |d OCLCQ  |d K6U  |d OCLCQ 
015 |a GBC180601  |2 bnb 
016 7 |a 020202624  |2 Uk 
020 |a 9780128210635  |q (electronic bk.) 
020 |a 012821063X  |q (electronic bk.) 
020 |z 9780128210628 
020 |z 0128210621 
035 |a (OCoLC)1261380194 
050 4 |a QD481 
082 0 4 |a 541.223  |2 23 
100 1 |a Karnik, Anil V. 
245 1 0 |a Stereochemistry :  |b a three-dimensional insight /  |c Anil V. Karnik, Mohammed Hasan. 
260 |a Amsterdam :  |b Elsevier,  |c 2021. 
300 |a 1 online resource 
336 |a text  |b txt  |2 rdacontent 
336 |a still image  |b sti  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
500 |a Includes index. 
505 0 |a Front Cover -- Stereochemistry -- Copyright Page -- Contents -- About the authors -- Foreword -- Preface -- I. Fundamentals of stereochemistry -- 1 Basic concepts of structure and stereochemistry -- 1.1 Introduction -- 1.2 A brief history -- 1.3 Molecular geometry -- 1.3.1 Van der Waals' radius -- 1.3.2 Bond length -- 1.3.3 Bond angle -- 1.3.4 Dihedral angle -- 1.4 Isomers -- 1.4.1 Conformational isomers -- 1.4.2 Configuration and configurational isomers -- 1.5 Projection formulae -- 1.5.1 Fischer projection -- 1.5.2 Newman projection -- 1.5.3 Sawhorse projection 
505 8 |a Questions and Problems -- References -- 3 Elements of chirality and chiral stereoisomerism -- 3.1 Introduction -- 3.2 Molecules with central chirality -- 3.2.1 Configurational descriptors for molecules with central chirality -- 3.2.1.1 The D-L system -- 3.2.1.2 The R/S system -- 3.3 Molecules with two or more chiral centres -- 3.3.1 Constitutionally unsymmetrical chiral molecules -- 3.3.1.1 Erythro and Threo -- 3.3.1.2 Pref and Parf -- 3.3.1.3 Like (l) and unlike (u) -- 3.3.1.4 Anti and Syn notations -- 3.3.1.5 Brewster's system 
505 8 |a 3.3.2 Stereoisomerism in constitutionally symmetrical chiral molecules -- 3.3.3 Stereoisomerism in cyclic molecules -- 3.4 Molecules with the presence of chiral axis -- 3.4.1 Assignment of configurational descriptors to molecules with presence of chiral axis -- 3.4.2 Allenes -- 3.4.3 Alkylidene cycloalkanes/Hemispiranes -- 3.4.4 Spiranes -- 3.4.5 Atropisomerism -- 3.4.6 Atropisomerism of biaryls, restricted rotation around sp2-sp2, C-C bond -- 3.4.7 Assignment of configurational descriptors to chiral biphenyls -- 3.4.8 Bridged biphenyls -- 3.5 Planar Chirality 
650 0 |a Stereochemistry. 
650 6 |a St�er�eochimie.  |0 (CaQQLa)201-0002577 
650 7 |a Stereochemistry.  |2 fast  |0 (OCoLC)fst01133138 
700 1 |a Hasan, Mohammed. 
776 0 8 |i Print version:  |z 0128210621  |z 9780128210628  |w (OCoLC)1237102163 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9780128210628  |z Texto completo