Steric and Stereoelectronic Effects in Organic Chemistry

The steric and stereoelectronic effects control the rate and stereochemical outcome of reactions. Hence, a decent understanding of the related concepts is essential for successful synthetic planning. The book attempts to address several important issues related to these concepts in a simplified mann...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριος συγγραφέας: Yadav, Veejendra K. (Συγγραφέας)
Συγγραφή απο Οργανισμό/Αρχή: SpringerLink (Online service)
Μορφή: Ηλεκτρονική πηγή Ηλ. βιβλίο
Γλώσσα:English
Έκδοση: Singapore : Springer Singapore : Imprint: Springer, 2016.
Θέματα:
Διαθέσιμο Online:Full Text via HEAL-Link
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020 |a 9789811011399  |9 978-981-10-1139-9 
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100 1 |a Yadav, Veejendra K.  |e author. 
245 1 0 |a Steric and Stereoelectronic Effects in Organic Chemistry  |h [electronic resource] /  |c by Veejendra K. Yadav. 
264 1 |a Singapore :  |b Springer Singapore :  |b Imprint: Springer,  |c 2016. 
300 |a XI, 211 p. 300 illus., 83 illus. in color.  |b online resource. 
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505 0 |a Steric and Stereoelectronic Control of Organic Molecular Structures and Organic Reactions -- Reactions at Saturated and Unsaturated Carbons -- Diastereoselectivity in Organic Reactions -- A(1,2) and A(1,3) Strains -- The Conservation of Orbital Symmetry (Woodward-Hoffmann Rules) -- The Overlap Component of the Stereoelectronic Factor vis-à-vis the Conservation of Orbital Symmetry Rules -- Miscellaneous. 
520 |a The steric and stereoelectronic effects control the rate and stereochemical outcome of reactions. Hence, a decent understanding of the related concepts is essential for successful synthetic planning. The book attempts to address several important issues related to these concepts in a simplified manner, and is intended for graduate students. It lays stress on the important aspects of steric and stereoelectronic effects and their control on the conformational profile and reactivity features. The book covers the geometrical requirements for reactions at saturated and unsaturated carbons in both cyclic and acyclic systems, and the resultant stereochemical features. The aspect of geometrical flexibility is also covered with a few examples involving intramolecular reactions. It deals with the facial selectivity of nucleophilic additions to acyclic and cyclic carbonyl compounds, and explains how the steric and stereoelectronic effects control the same. The work comments on allylic strains and their stereochemical control on different reactions with the related conformational control. It is a must read to understand the control elements, the prominent among these elements are spiro-conjugation, periselectivity, torquoselectivity, a-effect, Hammett’s substituent constants, Hammond postulate, and Curtin-Hammett principle. 
650 0 |a Chemistry. 
650 0 |a Organic chemistry. 
650 0 |a Physical chemistry. 
650 1 4 |a Chemistry. 
650 2 4 |a Organic Chemistry. 
650 2 4 |a Physical Chemistry. 
710 2 |a SpringerLink (Online service) 
773 0 |t Springer eBooks 
776 0 8 |i Printed edition:  |z 9789811011382 
856 4 0 |u http://dx.doi.org/10.1007/978-981-10-1139-9  |z Full Text via HEAL-Link 
912 |a ZDB-2-CMS 
950 |a Chemistry and Materials Science (Springer-11644)