000			03189nam a22004935i 4500
001			978-3-319-29773-6
003			DE-He213
005			20160615101139.0
007			cr nn 008mamaa
008			160426s2016 gw | s |||| 0|eng d
020			_a9783319297736 _9978-3-319-29773-6
024	7		_a10.1007/978-3-319-29773-6 _2doi
049			_aAlfaisal Main Library
050		4	_aQD415-436
072		7	_aPNN _2bicssc
072		7	_aSCI013040 _2bisacsh
082	0	4	_a547 _223
100	1		_aMamedov, Vakhid A. _eauthor.
245	1	0	_aQuinoxalines _h[electronic resource] : _bSynthesis, Reactions, Mechanisms and Structure / _cby Vakhid A. Mamedov.
264		1	_aCham : _bSpringer International Publishing : _bImprint: Springer, _c2016.
300			_aXV, 437 p. 591 illus., 546 illus. in color. _bonline resource.
336			_atext _btxt _2rdacontent
337			_acomputer _bc _2rdamedia
338			_aonline resource _bcr _2rdacarrier
347			_atext file _bPDF _2rda
505	0		_aIntroduction: Quinoxaline as a Parent Heterocycle -- Synthesis of Quinoxalines -- Synthesis of Pyrrolo[l,2-a]quinoxalines -- Synthesis of Imidazo[1,5-a]- and Imidazo[1,2-a]quinoxalines -- Synthesis of Quinoxaline Macrocycles -- Rearrangements of Quinoxalin(on)es in the Synthesis of Benzimidazol(on)es -- Appendix.
520			_aThis book reviews the fundamental aspects of quinoxaline chemistry: synthesis, reactions, mechanisms, structure, properties, and uses. The first four chapters present a survey of the developments in quinoxaline chemistry since the publication of the monograph on “Condensed Pyrazines” by Cheeseman and Cookson in 1979. These chapters give comprehensive coverage of all the methods of the synthesis of quinoxalines and the important quinoxaline-containing ring systems such as thiazolo[3,4-a]-, pyrrolo[1,2-a]-, and imidazo[1,5-a]quinoxalines. Chapter five describes many new methods for the construction of quinoxaline macrocycles, which are important in applications such as optical devices and materials. The final chapter reviews all previously known rearrangements of heterocyclic systems that lead to benzimidazole derivatives. Mamedov critically analyses these transformations to reveal a novel acid-catalyzed rearrangement of quinoxalinones giving 2-heteroarylbenzimidazoles and 1-heteroarylbenzimidazolones in the presence of nucleophilic reactants (MAMEDOV Heterocycle Rearrangement). This book is of interest to researchers in the fields of heterocyclic and synthetic organic chemistry. .
650		0	_aChemistry.
650		0	_aOrganic chemistry.
650		0	_aChemical engineering.
650		0	_aMedicinal chemistry.
650	1	4	_aChemistry.
650	2	4	_aOrganic Chemistry.
650	2	4	_aMedicinal Chemistry.
650	2	4	_aIndustrial Chemistry/Chemical Engineering.
655		7	_aElectronic books. _2local
710	2		_aSpringerLink (Online service)
773	0		_tSpringer eBooks
776	0	8	_iPrinted edition: _z9783319297712
856	4	0	_uhttp://ezproxy.alfaisal.edu/login?url=http://dx.doi.org/10.1007/978-3-319-29773-6
912			_aZDB-2-CMS
942			_2lcc _cEBOOKS
999			_c259621 _d259621