000			03845cam a2200565 i 4500
001			ocn951742623
003			OCoLC
005			20200827120531.0
006			m o d
007			cr |||||||||||
008			160613s2016 nyu ob 001 0 eng
010			_a 2016027315
040			_aDLC _beng _erda _cDLC _dOCLCF _dN$T _dEBLCP _dESU _dSNK _dDKU _dAUW _dMHW _dBTN _dIGB _dD6H _dVTS _dAGLDB _dAU@ _dG3B _dS8J _dS9I _dSTF _dDLC _dOCLCO
020			_a9781634856287 _q()
020			_a1634856287
020			_z9781634856041 (hardcover)
035			_a(OCoLC)951742623
042			_apcc
050	0	0	_aRC684.D52
060		4	_aQV 150
072		7	_aMED _x071000 _2bisacsh
082	0	0	_a615.7/1 _223
049			_aMAIN
245	0	0	_aNew research on dihydropyridines / _cJacquelyn Morales, editor.
264		1	_aNew York : _bNova Publishers, Inc., _c[2016]
300			_a1 online resource.
336			_atext _btxt _2rdacontent
337			_acomputer _bc _2rdamedia
338			_aonline resource _bcr _2rdacarrier
490	0		_aChemistry research and applications
504			_aIncludes bibliographical references and index.
588			_aDescription based on print version record and CIP data provided by publisher.
505	0		_aPreface; Recent Progress in the Synthesis of Dihydropyridines; Abstract; 1. Introduction; 2. Synthesis of Dyhydropyridines; 2.1. Multi-Component Coupling Reactions; 2.4. Miscellaneous; Outlook and Conclusion; Acknowledgments; References; Latest Research in the Synthesis of 1,4-Dihydropyridine Derivatives under Greener Reaction Conditions; Abstract; 1. Introduction; 2. Structure-Activity Relationship of 1,4-DHPs; 3. Pharmacological Activity of 1,4-DHPs; 4. Chemistry of 1,4-DHPs; 4.1. Hantzsch Dihydropyridine Synthesis and Other Synthetic Routes.
505	8		_a4.2. Catalyst-Free Synthesis of 1,4-DHPs4.3. Catalytic Synthesis of 1,4-DHPs; 4.3.1. Homogeneous Catalytic Synthesis of 1,4-DHPs; 4.3.1.1. Modified Hantzsch Synthesis; 4.3.1.1.1. Modified Hantzsch Synthesis through Route A; 4.3.1.1.2. Modified Hantzsch Synthesis through Route B; 4.3.1.1.3. Modified Hantzsch Synthesis through Route C; 4.3.1.1.4. Miscellaneous; 4.3.2. Heterogeneous Catalytic Synthesis of 1,4-DHPs; 4.4. Process Intensification for 1,4-DHPs Synthesis; Conclusion and Future Prospects; Acknowledgments; References.
505	8		_aSynthesis of Cyclic 1,4-Dihydropyridines Catalyzed by Fe(ClO4)3/SiO2Abstract; Introduction; Results and Discussion; Conclusion; Experimental; References; Synthesis of Chiral Dihydropyridines; Abstract; 1. Introduction; 2. Synthesis of 1,4-Dihydropyridines; 2.1. Thiazolidine-2-Thione as a Chiral Auxiliary; 2.3. Oxazolidine as a Chiral Auxiliary; 3. Synthesis of 1,2- and 1,6-Dihydropyridine Derivatives; 4. Synthesis of 1,4-Dihydroquinolines; 5. Synthetic Application of Dihydropyridines; Conclusion; References; Index.
590			_aeBooks on EBSCOhost _bEBSCO eBook Subscription Academic Collection - Worldwide
650		0	_aDihydropyridine. _0http://id.loc.gov/authorities/subjects/sh85037998
650		0	_aCalcium _xAntagonists. _0http://id.loc.gov/authorities/subjects/sh85018769
650		2	_aCalcium Channel Blockers.
650		7	_aMEDICAL _xPharmacology. _2bisacsh
650		7	_aCalcium _xAntagonists. _2fast _0(OCoLC)fst00844037
650		7	_aDihydropyridine. _2fast _0(OCoLC)fst00893778
655		4	_aElectronic books.
700	1		_aMorales, Jacquelyn, _eeditor.
776	0	8	_iPrint version: _tNew research on dihydropyridines _dHauppauge, New York : Nova Science Publishers, Inc., [2016] _z9781634856041 _w(DLC) 2016026171
856	4	0	_uhttps://libproxy.firstcity.edu.my:8443/login?url=http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=1356598
938			_aEBSCOhost _bEBSC _n1356598
938			_aEBL - Ebook Library _bEBLB _nEBL4698103
994			_a92 _bMYFCU
999			_c54319 _d54319