Synthesis of Functionalized Organoboron Compounds Through Copper(I) Catalysis

This book describes state-of-the-art borylation chemistry using copper(I) catalysis. Enantioselective reactions are included to afford a variety of functionalized, complex organoboronate esters, which will find wide application in asymmetric synthesis, drug discovery, and material science. Organobor...

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Bibliographic Details
Main Author: Kubota, Koji. (Author)
Corporate Author: SpringerLink (Online service)
Format: eBook
Language: English
Published: Singapore : Springer Singapore : Imprint: Springer, 2017.
Series: Springer Theses, Recognizing Outstanding Ph.D. Research,
Subjects:
Chemistry.
Organic chemistry.
Catalysis.
elektronické knihy
electronic books
ISBN: 9789811049354
Physical Description: 1 online resource (XIII, 213 p. 225 illus.)

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Table of contents

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020 |a 9789811049354 
024 7 |a 10.1007/978-981-10-4935-4  |2 doi 
100 1 |a Kubota, Koji.  |e author. 
245 1 0 |a Synthesis of Functionalized Organoboron Compounds Through Copper(I) Catalysis /  |c by Koji Kubota. 
264 1 |a Singapore :  |b Springer Singapore :  |b Imprint: Springer,  |c 2017. 
300 |a 1 online resource (XIII, 213 p. 225 illus.) 
336 |a text  |b txt  |2 rdacontent 
337 |a počítač  |b c  |2 rdamedia 
338 |a online zdroj  |b cr  |2 rdacarrier 
490 1 |a Springer Theses, Recognizing Outstanding Ph.D. Research,  |x 2190-5053 
505 0 |a General Introduction -- Copper(I)-Catalyzed Direct Boryl Substitution of Unactivated alkyl Halides -- Copper(I)-Catalyzed Intramolecular Borylative exo-Cyclization of Alkenyl Halides Containing Unactivated Double-Bond -- Copper(I)-Catalyzed Regio- and Enantioselective Monoborylation of Alkenylsilanes -- Copper(I)-Catalyzed Enantioselective Nucleophilic Borylation of Aldehydes -- Computational Insight into the Enantioselective Borylation of Aldehydes Cataluzed by Chiral Bisphosphine Copper(I) Complexes -- Copper(I)-Catalyzed Enantioselective Borylative Dearomatization of Indoles -- Copper(I)-Catalyzed Regio- and Enantioselective Borylation of 1,2-Dihydropyridines -- Summary and Outlook. 
506 |a Plný text je dostupný pouze z IP adres počítačů Univerzity Tomáše Bati ve Zlíně nebo vzdáleným přístupem pro zaměstnance a studenty 
520 |a This book describes state-of-the-art borylation chemistry using copper(I) catalysis. Enantioselective reactions are included to afford a variety of functionalized, complex organoboronate esters, which will find wide application in asymmetric synthesis, drug discovery, and material science. Organoboron compounds are recognized as useful reagents in organic synthesis; therefore, great effort has been devoted to the development of a simple, mild, and efficient method for their preparation in the past several years. However, the synthesis of functionalized organoboron compounds remains a challenging issue because known reactions often require the use of highly reactive organometallic carbon nucleophiles. This book focuses on conceptually new, formal nucleophilic copper(I)-catalyzed borylation reactions with diboron compounds that show high selectivity and excellent functional group compatibility. Theoretical studies based on density functional theory calculations to understand the reaction mechanisms have also been described. Advances in this novel borylation chemistry will allow the rapid and efficient synthesis of complex molecules with potentially interesting properties in combination with the boron functionalization process. . 
650 0 |a Chemistry. 
650 0 |a Organic chemistry. 
650 0 |a Catalysis. 
655 7 |a elektronické knihy  |7 fd186907  |2 czenas 
655 9 |a electronic books  |2 eczenas 
710 2 |a SpringerLink (Online service) 
776 0 8 |i Printed edition:  |z 9789811049347 
830 0 |a Springer Theses, Recognizing Outstanding Ph.D. Research,  |x 2190-5053 
856 4 0 |u https://proxy.k.utb.cz/login?url=http://dx.doi.org/10.1007/978-981-10-4935-4  |y Plný text 
992 |c NTK-SpringerCHEMS 
999 |c 100529  |d 100529 
993 |x NEPOSILAT  |y EIZ 

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