|
|
|
|
LEADER |
00000cam a2200000 a 4500 |
001 |
SCIDIR_on1261380194 |
003 |
OCoLC |
005 |
20231120010555.0 |
006 |
m o d |
007 |
cr |n||||||||| |
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
|