Biginelliova reakce (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Biginelliova reakce" in Czech language version.

refsWebsite

Global rank Czech rank

18doi.org

2^nd place

4^th place

4nih.gov

4^th place

8^th place

2zenodo.org

621^st place

2,192^nd place

2worldcat.org

5^th place

3^rd place

doi.org

dx.doi.org

P. Biginelli. Ueber Aldehyduramide des Acetessigäthers. Chemische Berichte. 1891, s. 1317–1319. Dostupné online. DOI 10.1002/cber.189102401228.
P. Biginelli. Ueber Aldehyduramide des Acetessigäthers. II. Chemische Berichte. 1891, s. 2962–2967. Dostupné online. DOI 10.1002/cber.189102402126.
H. E. Zaugg; W. B. Martin. Α-Amidoalkylations at Carbon. Organic Reactions. 1965, s. 88. ISBN 0471264180. DOI 10.1002/0471264180.or014.02.
C. O. Kappe. 100 years of the biginelli dihydropyrimidine synthesis. Tetrahedron. 1993, s. 6937–6963. ISBN 0471264180. DOI 10.1016/S0040-4020(01)87971-0.
C. O. Kappe; A. Stadler. The Biginelli Dihydropyrimidine Synthesis. Organic Reactions. 2004, s. 1–116. ISBN 0471264180. DOI 10.1002/0471264180.or063.01.
Dailei Song; Runxia Wang; Yongli Chen; Shaohua Zhang; Chunsheng Liu; Genxiang Luo. Reaction Kinetics and Catalysis Letters. Reaction Kinetics and Catalysis Letters. 2008, s. 385. DOI 10.1007/s11144-008-5379-2.
E. H. Hu; D. R. Sidler; U.-H. Dolling. Unprecedented Catalytic Three Component One-Pot Condensation Reaction: An Efficient Synthesis of 5-Alkoxycarbonyl- 4-aryl-3,4-dihydropyrimidin-2(1H)-ones. The Journal of Organic Chemistry. 1998, s. 3454. DOI 10.1021/jo970846u.
P. Wipf; A. Cunningham. A solid phase protocol of the biginelli dihydropyrimidine synthesis suitable for combinatorial chemistry. Tetrahedron Letters. 1995, s. 7819–7822. DOI 10.1016/0040-4039(95)01660-A.
C. O. Kappe. Highly versatile solid phase synthesis of biofunctional 4-aryl-3,4-dihydropyrimidines using resin-bound isothiourea building blocks and multidirectional resin cleavage. Bioorganic & Medicinal Chemistry Letters. 2000, s. 49–51. DOI 10.1016/S0960-894X(99)00572-7. PMID 10636241.
G. C. Rovnyak, K. S. Atwal, A. Hedberg, S., D. Kimball, S. Moreland, J. Z. Gougoutas, B. C. O'Reilly, J. Schwartz, M. F. Malley. Dihydropyrimidine calcium channel blockers. 4. Basic 3-substituted-4-aryl-1,4-dihydropyrimidine-5-carboxylic acid esters. Potent antihypertensive agents. Journal of Medicinal Chemistry. 1992, s. 3254–3263. DOI 10.1021/jm00095a023. PMID 1387168.
CRESPO, Abel; EL MAATOUGUI, Abdelaziz; BIAGINI, Pierfrancesco; AZUAJE, Jhonny; COELHO, Alberto; BREA, José; LOZA, María Isabel. Discovery of 3,4-Dihydropyrimidin-2(1H)-ones As a Novel Class of Potent and Selective A2B Adenosine Receptor Antagonists. ACS Medicinal Chemistry Letters. 2013-10-03, s. 1031–1036. ISSN 1948-5875. DOI 10.1021/ml400185v. PMID 24900602.
EL MAATOUGUI, Abdelaziz; AZUAJE, Jhonny; GONZÁLEZ-GÓMEZ, Manuel; MIGUEZ, Gabriel; CRESPO, Abel; CARBAJALES, Carlos; ESCALANTE, Luz. Discovery of Potent and Highly Selective A2B Adenosine Receptor Antagonist Chemotypes. Journal of Medicinal Chemistry. 2016-03-10, s. 1967–1983. ISSN 0022-2623. DOI 10.1021/acs.jmedchem.5b01586. PMID 26824742.
K. Folkers; T. B. Johnson. Researches on Pyrimidines. CXXXVI. The Mechanism of Formation of Tetrahydropyrimidines by the Biginelli Reaction1. Journal of the American Chemical Society. 1933, s. 3784–3791. DOI 10.1021/ja01336a054.
F. Sweet; J. D. Fissekis. Synthesis of 3,4-dihydro-2(1H)-pyrimidinones and the mechanism of the Biginelli reaction. Journal of the American Chemical Society. 1973, s. 8741–8749. DOI 10.1021/ja00807a040.
C. O. Kappe. A Reexamination of the Mechanism of the Biginelli Dihydropyrimidine Synthesis. Support for anN-Acyliminium Ion Intermediate. The Journal of Organic Chemistry. 1997, s. 7201–7204. DOI 10.1021/jo971010u.
B. C. O'Reilly; K. S. Atwal. Synthesis of Substituted 1,2,3,4-Tetrahydro-6-methyl-2-oxo-5-pyrimidinecarboxylic Acid Esters: The Biginelli Condensation Revisited. Heterocycles. 1987, s. 1185–1188. DOI 10.3987/R-1987-05-1185.
B. C. O'Reilly; K. S. Atwal. Synthesis of Substituted 1,2,3,4-Tetrahydro-6-methyl-2-thioxo-5-pyrimidinecarboxylic Acid Esters: The Biginelli Condensation Revisited. Heterocycles. 1987, s. 1189–1192. DOI 10.3987/R-1987-05-1189.
Atul Kumar; Ram Awatar Maurya. An efficient bakers' yeast catalyzed synthesis of 3,4-dihydropyrimidin-2-(1H)-ones. Tetrahedron Letters. 2007, s. 4569. DOI 10.1016/j.tetlet.2007.04.130.

nih.gov

ncbi.nlm.nih.gov

C. O. Kappe. Highly versatile solid phase synthesis of biofunctional 4-aryl-3,4-dihydropyrimidines using resin-bound isothiourea building blocks and multidirectional resin cleavage. Bioorganic & Medicinal Chemistry Letters. 2000, s. 49–51. DOI 10.1016/S0960-894X(99)00572-7. PMID 10636241.
G. C. Rovnyak, K. S. Atwal, A. Hedberg, S., D. Kimball, S. Moreland, J. Z. Gougoutas, B. C. O'Reilly, J. Schwartz, M. F. Malley. Dihydropyrimidine calcium channel blockers. 4. Basic 3-substituted-4-aryl-1,4-dihydropyrimidine-5-carboxylic acid esters. Potent antihypertensive agents. Journal of Medicinal Chemistry. 1992, s. 3254–3263. DOI 10.1021/jm00095a023. PMID 1387168.
CRESPO, Abel; EL MAATOUGUI, Abdelaziz; BIAGINI, Pierfrancesco; AZUAJE, Jhonny; COELHO, Alberto; BREA, José; LOZA, María Isabel. Discovery of 3,4-Dihydropyrimidin-2(1H)-ones As a Novel Class of Potent and Selective A2B Adenosine Receptor Antagonists. ACS Medicinal Chemistry Letters. 2013-10-03, s. 1031–1036. ISSN 1948-5875. DOI 10.1021/ml400185v. PMID 24900602.
EL MAATOUGUI, Abdelaziz; AZUAJE, Jhonny; GONZÁLEZ-GÓMEZ, Manuel; MIGUEZ, Gabriel; CRESPO, Abel; CARBAJALES, Carlos; ESCALANTE, Luz. Discovery of Potent and Highly Selective A2B Adenosine Receptor Antagonist Chemotypes. Journal of Medicinal Chemistry. 2016-03-10, s. 1967–1983. ISSN 0022-2623. DOI 10.1021/acs.jmedchem.5b01586. PMID 26824742.

worldcat.org

CRESPO, Abel; EL MAATOUGUI, Abdelaziz; BIAGINI, Pierfrancesco; AZUAJE, Jhonny; COELHO, Alberto; BREA, José; LOZA, María Isabel. Discovery of 3,4-Dihydropyrimidin-2(1H)-ones As a Novel Class of Potent and Selective A2B Adenosine Receptor Antagonists. ACS Medicinal Chemistry Letters. 2013-10-03, s. 1031–1036. ISSN 1948-5875. DOI 10.1021/ml400185v. PMID 24900602.
EL MAATOUGUI, Abdelaziz; AZUAJE, Jhonny; GONZÁLEZ-GÓMEZ, Manuel; MIGUEZ, Gabriel; CRESPO, Abel; CARBAJALES, Carlos; ESCALANTE, Luz. Discovery of Potent and Highly Selective A2B Adenosine Receptor Antagonist Chemotypes. Journal of Medicinal Chemistry. 2016-03-10, s. 1967–1983. ISSN 0022-2623. DOI 10.1021/acs.jmedchem.5b01586. PMID 26824742.

zenodo.org

P. Biginelli. Ueber Aldehyduramide des Acetessigäthers. Chemische Berichte. 1891, s. 1317–1319. Dostupné online. DOI 10.1002/cber.189102401228.
P. Biginelli. Ueber Aldehyduramide des Acetessigäthers. II. Chemische Berichte. 1891, s. 2962–2967. Dostupné online. DOI 10.1002/cber.189102402126.