000			03275nam a22004935i 4500
001			978-3-642-12675-8
003			DE-He213
005			20140220084535.0
007			cr nn 008mamaa
008			100721s2010 gw | s |||| 0|eng d
020			_a9783642126758 _9978-3-642-12675-8
024	7		_a10.1007/978-3-642-12675-8 _2doi
050		4	_aQD415-436
072		7	_aPNN _2bicssc
072		7	_aSCI013040 _2bisacsh
082	0	4	_a547 _223
100	1		_aOrru, Romano V. A. _eeditor.
245	1	0	_aSynthesis of Heterocycles via Multicomponent Reactions I _h[electronic resource] / _cedited by Romano V. A. Orru, Eelco Ruijter.
264		1	_aBerlin, Heidelberg : _bSpringer Berlin Heidelberg : _bImprint: Springer, _c2010.
300			_aXV, 280p. 87 illus. _bonline resource.
336			_atext _btxt _2rdacontent
337			_acomputer _bc _2rdamedia
338			_aonline resource _bcr _2rdacarrier
347			_atext file _bPDF _2rda
490	1		_aTopics in Heterocyclic Chemistry, _x1861-9282 ; _v23
505	0		_aSynthesis of Heterocycles Through Classical Ugi and Passerini Reactions Followed by Secondary Transformations Involving One or Two Additional Functional Groups -- Aminoazoles as Key Reagents in Multicomponent Heterocyclizations -- The Piperazine Space in Isocyanide-based MCR Chemistry -- ?-Acidic Isocyanides in Multicomponent Chemistry -- Microreactor Technology as an Efficient Tool for Multicomponent Reactions -- Cyclic Peptidomimetics and Pseudopeptides from Multicomponent Reactions -- ?-Diketo Building Blocks for MCRs-Based Syntheses of Heterocycles.
520			_aContents: L. Banfi ∙ A. Basso ∙ R. Riva: Synthesis of Heterocycles Through Classical Ugi and Passerini Reactions Followed by Secondary Transformations Involving One or Two Additional Functional Groups.- V.A. Chebanov ∙ K. A. Gura ∙ S.M. Desenko: Aminoazoles as Key Reagents in Multicomponent Heterocyclizations.- Y. Huang ∙ K. Khoury ∙ A. Dömling: Piperazine Scaffolds by Multicomponent 3 Reactions: The Piperazine Space 4 in MCR Chemistry 5 Deep MCR Piperazine Space.- N. Elders ∙ E. Ruijter ∙ V.G. Nenajdenko ∙ R.V.A. Orru: α-Acidic Isocyanides in Multicomponent Chemistry.- A. Cukalovic ∙ J.-C.M.R. Monbaliu ∙ C.V. Stevens: Microreactor Technology as an Efficient Tool for Multicomponent Reactions.- L.A. Wessjohann ∙ C.R.B. Rhoden ∙ D.G. Rivera ∙ O. Eichler Vercillo: Cyclic Peptidomimetics and Pseudopeptides from Multicomponent Reactions.- M. del Mar Sanchez Duque ∙ C. Allais ∙ N. Isambert ∙ T. Constantieux ∙ J. Rodriguez: ß-Diketo Building Blocks for MCRs-Based Syntheses of Heterocycles
650		0	_aChemistry.
650		0	_aBiochemical engineering.
650		0	_aChemistry, Organic.
650		0	_aBiochemistry.
650	1	4	_aChemistry.
650	2	4	_aOrganic Chemistry.
650	2	4	_aBiochemical Engineering.
650	2	4	_aMedicinal Chemistry.
700	1		_aRuijter, Eelco. _eeditor.
710	2		_aSpringerLink (Online service)
773	0		_tSpringer eBooks
776	0	8	_iPrinted edition: _z9783642126741
830		0	_aTopics in Heterocyclic Chemistry, _x1861-9282 ; _v23
856	4	0	_uhttp://dx.doi.org/10.1007/978-3-642-12675-8
912			_aZDB-2-CMS
999			_c112122 _d112122