Stereoelectronic Effects: A Bridge Between Structure and Reactivity
Igor V. Alabugin
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Description for Stereoelectronic Effects: A Bridge Between Structure and Reactivity
Paperback. Num Pages: 392 pages. BIC Classification: PNRH; TDCB. Category: (P) Professional & Vocational. Dimension: 191 x 254 x 20. Weight in Grams: 834.
Stereoelectronic Effects illustrates the utility of stereoelectronic concepts using structure and reactivity of organic molecules
- An advanced textbook that provides an up-to-date overview of the field, starting from the fundamental principles
- Presents a large selection of modern examples of stereoelectronic effects in organic reactivity
- Shows practical applications of stereoelectronic effects in asymmetric catalysis, photochemical processes, bioorganic chemistry and biochemistry, inorganic and organometallic reactivity, supramolecular chemistry and materials science
Product Details
Publisher
John Wiley & Sons Inc
Format
Paperback
Publication date
2016
Condition
New
Number of Pages
400
Place of Publication
New York, United States
ISBN
9781118906347
SKU
V9781118906347
Shipping Time
Usually ships in 7 to 11 working days
Ref
99-50
About Igor V. Alabugin
Professor Igor V. Alabugin, Department of Chemistry and Biochemistry, Florida State University, USA Over the last 12 years, Professor Alabugin has published a body of work dedicated to stereoelectronic effects and applied these concepts in practice to the development of new organic reactions. The wide appeal of these concepts is reflected in a large number citations for his papers ... Read more
Reviews for Stereoelectronic Effects: A Bridge Between Structure and Reactivity
"This book is highly recommended to every chemist and particularly to every student to work through this book. The higher understanding thus obtained in many chemical fields will be beneficial throughout every phase of chemical education and work. It should furthermore be perfectly suitable as accompanying book for an advanced course on this topic." (Angewandte, 1 February 2017)