|
|
|
|
| LEADER |
00000cam a2200000 i 4500 |
| 001 |
EBSCO_ocn951742623 |
| 003 |
OCoLC |
| 005 |
20231017213018.0 |
| 006 |
m o d |
| 007 |
cr ||||||||||| |
| 008 |
160613s2016 nyu ob 001 0 eng |
| 010 |
|
|
|a 2016027315
|
| 040 |
|
|
|a DLC
|b eng
|e rda
|c DLC
|d OCLCF
|d N$T
|d EBLCP
|d ESU
|d SNK
|d DKU
|d AUW
|d MHW
|d BTN
|d IGB
|d D6H
|d VTS
|d AGLDB
|d AU@
|d G3B
|d S8J
|d S9I
|d STF
|d DLC
|d OCLCO
|d OCLCQ
|d OCLCO
|
| 020 |
|
|
|a 9781634856287
|q ()
|
| 020 |
|
|
|a 1634856287
|
| 020 |
|
|
|z 9781634856041 (hardcover)
|
| 035 |
|
|
|a (OCoLC)951742623
|
| 042 |
|
|
|a pcc
|
| 050 |
0 |
0 |
|a RC684.D52
|
| 060 |
|
4 |
|a QV 150
|
| 072 |
|
7 |
|a MED
|x 071000
|2 bisacsh
|
| 082 |
0 |
0 |
|a 615.7/1
|2 23
|
| 049 |
|
|
|a UAMI
|
| 245 |
0 |
0 |
|a New research on dihydropyridines /
|c Jacquelyn Morales, editor.
|
| 264 |
|
1 |
|a New York :
|b Nova Publishers, Inc.,
|c [2016]
|
| 300 |
|
|
|a 1 online resource.
|
| 336 |
|
|
|a text
|b txt
|2 rdacontent
|
| 337 |
|
|
|a computer
|b c
|2 rdamedia
|
| 338 |
|
|
|a online resource
|b cr
|2 rdacarrier
|
| 490 |
0 |
|
|a Chemistry research and applications
|
| 504 |
|
|
|a Includes bibliographical references and index.
|
| 588 |
|
|
|a Description based on print version record and CIP data provided by publisher.
|
| 505 |
0 |
|
|a Preface; 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 |
|
|a 4.2. 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 |
|
|a Synthesis 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 |
|
|
|a eBooks on EBSCOhost
|b EBSCO eBook Subscription Academic Collection - Worldwide
|
| 650 |
|
0 |
|a Dihydropyridine.
|
| 650 |
|
0 |
|a Calcium
|x Antagonists.
|
| 650 |
|
2 |
|a Calcium Channel Blockers
|
| 650 |
|
2 |
|a Dihydropyridines
|
| 650 |
|
6 |
|a Dihydropyridines.
|
| 650 |
|
6 |
|a Calcium
|x Antagonistes.
|
| 650 |
|
7 |
|a MEDICAL
|x Pharmacology.
|2 bisacsh
|
| 650 |
|
7 |
|a Calcium
|x Antagonists
|2 fast
|
| 650 |
|
7 |
|a Dihydropyridine
|2 fast
|
| 700 |
1 |
|
|a Morales, Jacquelyn,
|e editor.
|
| 776 |
0 |
8 |
|i Print version:
|t New research on dihydropyridines
|d Hauppauge, New York : Nova Science Publishers, Inc., [2016]
|z 9781634856041
|w (DLC) 2016026171
|
| 856 |
4 |
0 |
|u https://ebsco.uam.elogim.com/login.aspx?direct=true&scope=site&db=nlebk&AN=1356598
|z Texto completo
|
| 938 |
|
|
|a EBSCOhost
|b EBSC
|n 1356598
|
| 938 |
|
|
|a EBL - Ebook Library
|b EBLB
|n EBL4698103
|
| 994 |
|
|
|a 92
|b IZTAP
|
