-
1
-
-
84898855875
-
Task-specific ionic liquid incorporating anionic heteropolyacid-catalyzed Hantzsch and Mannich multicomponent reactions. Ionic liquid effect probed by ESIMS (/MS)
-
Alvim, H. G. O.; Bataglion, G. A.; Ramos, L. M.; De Oliveira, A. L.; De Oliveira, H. C. B.; Eberlin, M. N.; De Macedo, J. L.; Da Silva, W. A.; Neto, B. A. D. Task-specific ionic liquid incorporating anionic heteropolyacid-catalyzed Hantzsch and Mannich multicomponent reactions. Ionic liquid effect probed by ESIMS (/MS), Tetrahedron, 2014, 70, 3306-3313.
-
(2014)
Tetrahedron
, vol.70
, pp. 3306-3313
-
-
Alvim, H.G.O.1
Bataglion, G.A.2
Ramos, L.M.3
De Oliveira, A.L.4
De Oliveira, H.C.B.5
Eberlin, M.N.6
De Macedo, J.L.7
Da Silva, W.A.8
Neto, B.A.D.9
-
2
-
-
79955884563
-
Room-temperature ionic liquids: Solvents for synthesis and catalysis
-
Hallet, J. P.; Welton, T. Room-Temperature Ionic Liquids: Solvents for Synthesis and Catalysis. 2. Chem. Rev., 2011, 111, 3508-3576.
-
(2011)
2. Chem. Rev.
, vol.111
, pp. 3508-3576
-
-
Hallet, J.P.1
Welton, T.2
-
3
-
-
38349122534
-
Toxicity and biodegradability of imidazolium ionic liquids
-
(a) Romero, A.; Santos, A.; Tojo, J.; Rodrýguez, A. Toxicity and biodegradability of imidazolium ionic liquids. J. Hazard. Mater., 2008, 151, 268-273;
-
(2008)
J. Hazard. Mater.
, vol.151
, pp. 268-273
-
-
Romero, A.1
Santos, A.2
Tojo, J.3
Rodrýguez, A.4
-
5
-
-
84855806743
-
Exerted influence of deep eutectic solvent concentration in the room temperature ionic conductivity and thermal behavior of corn starch based polymer electrolytes
-
(c) Ramesh, S.; Shanti, R. Exerted influence of deep eutectic solvent concentration in the room temperature ionic conductivity and thermal behavior of corn starch based polymer electrolytes. Journal of Molecular Liquids, 2012, 166, 40-43.
-
(2012)
Journal of Molecular Liquids
, vol.166
, pp. 40-43
-
-
Ramesh, S.1
Shanti, R.2
-
6
-
-
33846227529
-
Ionic liquids: First direct determination of their cohesive energy
-
Santos, J.; Lopes, J.; Coutinho, J.; Esperança, J.; Gomes, L.; Marrucho, I.; Rebelo, L. Ionic Liquids: First Direct Determination of their Cohesive Energy. J. Am. Chem. Soc., 2007, 129, 284.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 284
-
-
Santos, J.1
Lopes, J.2
Coutinho, J.3
Esperança, J.4
Gomes, L.5
Marrucho, I.6
Rebelo, L.7
-
7
-
-
80051585686
-
Environmentally benign and energy efficient methodology for condensation: An interesting facet to the classical Perkin reaction
-
(a) Pawar, P. M.; Jarag, K. J.; Shankarling, G. S. Environmentally benign and energy efficient methodology for condensation: an interesting facet to the classical Perkin reaction. Green Chem. 2011, 13, 2130-2134;
-
(2011)
Green Chem
, vol.13
, pp. 2130-2134
-
-
Pawar, P.M.1
Jarag, K.J.2
Shankarling, G.S.3
-
8
-
-
84879492207
-
Efficient deep eutectic solvents catalyzed synthesis of pyran and benzopyran derivatives
-
(b) Azizi, N.; Dezfooli, S.; Khajeh, M.; Hashemi, M. M. Efficient deep eutectic solvents catalyzed synthesis of pyran and benzopyran derivatives. Journal of Molecular Liquids, 2013, 186, 76-80.
-
(2013)
Journal of Molecular Liquids
, vol.186
, pp. 76-80
-
-
Azizi, N.1
Dezfooli, S.2
Khajeh, M.3
Hashemi, M.M.4
-
9
-
-
79952481457
-
Processing of metals and metal oxides using ionic liquids
-
(a) Abbott, A. P.; Frisch, G.; Hartley, J.; Ryder, K. S. Processing of metals and metal oxides using ionic liquids. Green Chem., 2011, 13, 471-481;
-
(2011)
Green Chem.
, vol.13
, pp. 471-481
-
-
Abbott, A.P.1
Frisch, G.2
Hartley, J.3
Ryder, K.S.4
-
10
-
-
78651289933
-
Glycerol eutectic as sustainable solvent systems
-
(b) Abbott, A. P.; Harris, R. C.; Ryder, K. S.; Agostino, C. D.; Gladden, L. F.; Mantle, M. D. Glycerol eutectic as sustainable solvent systems. Green Chem., 2011, 13, 82-90;
-
(2011)
Green Chem.
, vol.13
, pp. 82-90
-
-
Abbott, A.P.1
Harris, R.C.2
Ryder, K.S.3
Agostino, C.D.4
Gladden, L.F.5
Mantle, M.D.6
-
11
-
-
84859138437
-
Novel choline-chloride-based deepeutecticsolvents with renewablehydrogen bond donors: Levulinic acid and sugar-based polyols
-
(c) Maugeri, Z.; Domýnguez De Marýa, P. Novel choline-chloride-based deepeutecticsolvents with renewablehydrogen bond donors: levulinic acid and sugar-based polyols. RSC Adv., 2012, 2, 421-425;
-
(2012)
RSC Adv.
, vol.2
, pp. 421-425
-
-
Maugeri, Z.1
Domýnguez De Marýa, P.2
-
12
-
-
84880045740
-
Organic synthesis in deep eutectic solvents: Paal-Knorr reactions
-
(d) Handy, S.; Lavender, K. Organic synthesis in deep eutectic solvents: Paal-Knorr reactions. Tetrahedron Lett., 2013, 54, 4377-4379.
-
(2013)
Tetrahedron Lett.
, vol.54
, pp. 4377-4379
-
-
Handy, S.1
Lavender, K.2
-
13
-
-
58549102475
-
5-Substituted pyrido[2, 3-d]pyrimidine, an inhibitor against three receptor tyrosine kinases
-
(a) Kammasud, N.; Boonyarat, C.; Sanphanya, K. 5-Substituted pyrido[2, 3-d]pyrimidine, an inhibitor against three receptor tyrosine kinases. Bioorg. Med. Chem. Lett., 2009, 19, 745-750;
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 745-750
-
-
Kammasud, N.1
Boonyarat, C.2
Sanphanya, K.3
-
14
-
-
0012907461
-
A novel pyridopyrimidine inhibitor of abl kinase is a picomolar inhibitor of Bcr-abl-driven K562 cells and is effective against STI571-resistant Bcr-abl mutants
-
(b) Huron, D. R.; Gorre, M. E.; Kraker, A. J.; Sawyers, C. L.; Rosen, N.; Moasser, M. M. A novel pyridopyrimidine inhibitor of abl kinase is a picomolar inhibitor of Bcr-abl-driven K562 cells and is effective against STI571-resistant Bcr-abl mutants. Clin. Cancer Res., 2003, 9, 1267-1273;
-
(2003)
Clin. Cancer Res.
, vol.9
, pp. 1267-1273
-
-
Huron, D.R.1
Gorre, M.E.2
Kraker, A.J.3
Sawyers, C.L.4
Rosen, N.5
Moasser, M.M.6
-
15
-
-
0029990447
-
2, 4-diamino-5-deaza-6-substituted pyrido[2, 3-d]pyrimidine antifolates as potent and selective nonclassical inhibitors of dihydrofolate reductases
-
(c) Gangjee, A.; Vasudevan, A.; Queener, S. F.; Kisliuk, R. L. 2, 4-diamino-5-deaza-6-substituted pyrido[2, 3-d]pyrimidine antifolates as potent and selective nonclassical inhibitors of dihydrofolate reductases. J. Med. Chem., 1996, 39, 1438-1446;
-
(1996)
J. Med. Chem.
, vol.39
, pp. 1438-1446
-
-
Gangjee, A.1
Vasudevan, A.2
Queener, S.F.3
Kisliuk, R.L.4
-
16
-
-
65149102947
-
Novel pyridopyrimidine derivatives as inhibitors of stable toxin a (STa) induced cGMP synthesis
-
(d) Tanifum, E. A.; Kots, A. Y.; Choi, B.-K.; Murad, F.; Gilbertson, S. R. Novel pyridopyrimidine derivatives as inhibitors of stable toxin a (STa) induced cGMP synthesis. Biorg. Med. Chem. Lett., 2009, 19, 3067-3071;
-
(2009)
Biorg. Med. Chem. Lett.
, vol.19
, pp. 3067-3071
-
-
Tanifum, E.A.1
Kots, A.Y.2
Choi, B.-K.3
Murad, F.4
Gilbertson, S.R.5
-
17
-
-
70349256453
-
The discovery and optimisation of pyrido[2, 3-d]pyrimidine-2, 4-diamines as potent and selective inhibitors of mTOR kinase
-
(e) Malaga, K.; Duggan, H.; Menear, K. The discovery and optimisation of pyrido[2, 3-d]pyrimidine-2, 4-diamines as potent and selective inhibitors of mTOR kinase. Bioorg. Med. Chem. Lett., 2009, 19, 5950-5953;
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 5950-5953
-
-
Malaga, K.1
Duggan, H.2
Menear, K.3
-
18
-
-
20244366405
-
Pyrido[2, 3-d]pyrimidin-7-ones as specific inhibitors of cyclin-dependent kinase 4
-
(f) VanderWel, S. N.; Harvey, P. J.; McNamara, D. J.; Repine, J. T.; Keller, P. R.; Quin, J.,; Booth, R. J.; Elliott, W. L.; Dobrusin, E. M.; Fry, D. W.; Toogood, P. L. Pyrido[2, 3-d]pyrimidin-7-ones as specific inhibitors of cyclin-dependent kinase 4. J. Med. Chem., 2005, 48, 2371-2387;
-
(2005)
J. Med. Chem.
, vol.48
, pp. 2371-2387
-
-
Vander Wel, S.N.1
Harvey, P.J.2
McNamara, D.J.3
Repine, J.T.4
Keller, P.R.5
Quin, J.6
Booth, R.J.7
Elliott, W.L.8
Dobrusin, E.M.9
Fry, D.W.10
Toogood, P.L.11
-
19
-
-
84855819783
-
Sulfur and selenium derivatives of quinazoline and pyrido[2, 3-d]pyrimidine: Synthesis and study of their potential cytotoxic activity in vitro
-
(g) Moreno, E.; Plano, D.; Lamberto, I.; Font, M.; Enico, I.; Palop, J. A.; Martin, C. S. Sulfur and selenium derivatives of quinazoline and pyrido[2, 3-d]pyrimidine: Synthesis and study of their potential cytotoxic activity in vitro. Eur. J. Med. Chem., 2012, 47, 283-298;
-
(2012)
Eur. J. Med. Chem.
, vol.47
, pp. 283-298
-
-
Moreno, E.1
Plano, D.2
Lamberto, I.3
Font, M.4
Enico, I.5
Palop, J.A.6
Martin, C.S.7
-
20
-
-
10644256476
-
KF-alumina catalyzed one-pot synthesis of pyrido[2, 3-d]pyrimidine derivatives
-
(h) Wang, X. S.; Zeng, Z. S.; Shi, D. Q.; Wei, X. Y.; Zong, Z. M. KF-Alumina Catalyzed One-Pot Synthesis of Pyrido[2, 3-d]Pyrimidine Derivatives. Synth. Commun., 2004, 34, 4331-4337;
-
(2004)
Synth. Commun.
, vol.34
, pp. 4331-4337
-
-
Wang, X.S.1
Zeng, Z.S.2
Shi, D.Q.3
Wei, X.Y.4
Zong, Z.M.5
-
21
-
-
60649098957
-
Synthesis of new 2-substituted pyrido[2, 3-d]pyrimidin-4 (1H)-ones and their antibacterial activity
-
(i) Narayana, B. L.; Rao, A. R. R.; Rao, P. S. Synthesis of new 2-substituted pyrido[2, 3-d]pyrimidin-4 (1H)-ones and their antibacterial activity. Eur. J. Med. Chem., 2009, 44, 1369-1376;
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 1369-1376
-
-
Narayana, B.L.1
Rao, A.R.R.2
Rao, P.S.3
-
22
-
-
67649160744
-
Synthesis of 4-substituted pyrido[2, 3-d]pyrimidin-4 (1H)-one as analgesic and antiinflammatory agents
-
(j) El-Gazzar, A. B. A.; Hafez, H. N. Synthesis of 4-substituted pyrido[2, 3-d]pyrimidin-4 (1H)-one as analgesic and antiinflammatory agents. Bioorg. Med. Chem. Lett., 2009, 19, 3392-3397;
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 3392-3397
-
-
El-Gazzar, A.B.A.1
Hafez, H.N.2
-
23
-
-
33847784997
-
Biological profile of new apoptotic agents based on 2, 4-pyrido[2, 3-d]pyrimidine derivatives
-
(k) Cordeu, L.; Cubedo, E.; Bandres, E.; Rebollo, A.; Saenz, X.; Chozes, H. M.; Dominquez, V.; Echeverria, M.; Mendivil, B.; Sanmartin, C.; Palop, J. A.; Font, M.; Garcia-Foncillas, J. Biological profile of new apoptotic agents based on 2, 4-pyrido[2, 3-d]pyrimidine derivatives. Bioorg. Med. Chem., 2007, 15, 1659-1669;
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 1659-1669
-
-
Cordeu, L.1
Cubedo, E.2
Bandres, E.3
Rebollo, A.4
Saenz, X.5
Chozes, H.M.6
Dominquez, V.7
Echeverria, M.8
Mendivil, B.9
Sanmartin, C.10
Palop, J.A.11
Font, M.12
Garcia-Foncillas, J.13
-
24
-
-
0025691476
-
-
(l) Ahluwalia, V. K.; Bhatla, R.; Khurana, A.; Kumar, R. Indian J. Chem. Sect. B, 1990, 29, 1141;
-
(1990)
Indian J. Chem. Sect. B
, vol.29
, pp. 1141
-
-
Ahluwalia, V.K.1
Bhatla, R.2
Khurana, A.3
Kumar, R.4
-
25
-
-
46149094634
-
Pyridopyrimidine derivatives as inhibitors of cyclic nucleotide synthesis: Application for treatment of diarrhea
-
(m) Kots, A. Y.; Choi, B.-K.; Estrella-Jimenez, M. E.; Warren, C. A.; Gilbertson, S. R.; Guerrant, R. L.; Murad, F. Pyridopyrimidine derivatives as inhibitors of cyclic nucleotide synthesis: Application for treatment of diarrhea. Proc. Natl. Acad. Sci., 2008, 105, 8440-8445.
-
(2008)
Proc. Natl. Acad. Sci.
, vol.105
, pp. 8440-8445
-
-
Kots, A.Y.1
Choi, B.-K.2
Estrella-Jimenez, M.E.3
Warren, C.A.4
Gilbertson, S.R.5
Guerrant, R.L.6
Murad, F.7
-
26
-
-
0015511678
-
Pyrido (2, 3-d) pyrimidines. 3. Synthesis of some 8-(-D-ribofuranosyl) pyrido (2, 3-d) pyrimidines structurally related to the antibiotic sangivamycin
-
Rizkalla, B. H.; Broom, A. D. J. Pyrido (2, 3-d) pyrimidines. 3. Synthesis of some 8-(-D-ribofuranosyl) pyrido (2, 3-d) pyrimidines structurally related to the antibiotic sangivamycin. J. Org. Chem., 1972, 37, 3980-3985.
-
(1972)
J. Org. Chem.
, vol.37
, pp. 3980-3985
-
-
Rizkalla, B.H.1
Broom, A.D.J.2
-
27
-
-
84913545663
-
Recent advances in the synthesis of biologically active spirooxindoles
-
Press, Accepted Manuscript
-
(a) Santos, M. M. M. Recent advances in the synthesis of biologically active spirooxindoles. Tetrahedron, 2014 (In Press, Accepted Manuscript, Available online);
-
(2014)
Tetrahedron
-
-
Santos, M.M.M.1
-
28
-
-
84905924558
-
The use of spirocyclic scaffolds in drug discovery
-
(b) Zheng, Y.; Tice, C. M.; Singh, S. B. The use of spirocyclic scaffolds in drug discovery. Bioorganic & Medicinal Chemistry Letters, 2014, 24, 3673-3682;
-
(2014)
Bioorganic & Medicinal Chemistry Letters
, vol.24
, pp. 3673-3682
-
-
Zheng, Y.1
Tice, C.M.2
Singh, S.B.3
-
29
-
-
84869188848
-
Isatins as privileged molecules in design and synthesis of spiro-fused cyclic frameworks
-
(c) Singh, G. S.; Desta, Z. Y. Isatins As Privileged Molecules in Design and Synthesis of Spiro-Fused Cyclic Frameworks. Chem. Rev., 2012, 112, 6104-6155.
-
(2012)
Chem. Rev.
, vol.112
, pp. 6104-6155
-
-
Singh, G.S.1
Desta, Z.Y.2
-
30
-
-
84855797583
-
Synthesis and QSAR study of novel cytotoxic spiro[3H-indole-3, 2" (1"H) - Pyrrolo[3, 4-c]pyrrole]-2, 3", 5" (1H, 2"aH, 4"H)-triones
-
(a) Girgis, A. S.; Stawinski, J.; Ismail, N. S.; Farag, H. Synthesis and QSAR study of novel cytotoxic spiro[3H-indole-3, 2" (1"H) - pyrrolo[3, 4-c]pyrrole]-2, 3", 5" (1H, 2"aH, 4"H)-triones. Eur. J. Med. Chem., 2012, 47, 312-322;
-
(2012)
Eur. J. Med. Chem.
, vol.47
, pp. 312-322
-
-
Girgis, A.S.1
Stawinski, J.2
Ismail, N.S.3
Farag, H.4
-
31
-
-
84874657033
-
Facile one-pot synthesis of novel dispirooxindole-pyrrolidine derivatives and their antimicrobial and anticancer activity against A549 human lung adenocarcinoma cancer cell line
-
(b) Arun, Y.; Bhaskar, G.; Balachandran, C.; Ignacimuthu, S.; Perumal, P. T. Facile one-pot synthesis of novel dispirooxindole-pyrrolidine derivatives and their antimicrobial and anticancer activity against A549 human lung adenocarcinoma cancer cell line. Bioorganic & Medicinal Chemistry Letters, 2013, 23, 1839-1845;
-
(2013)
Bioorganic & Medicinal Chemistry Letters
, vol.23
, pp. 1839-1845
-
-
Arun, Y.1
Bhaskar, G.2
Balachandran, C.3
Ignacimuthu, S.4
Perumal, P.T.5
-
32
-
-
84868526878
-
Discovery and optimization of a novel spiropyrrolidine inhibitor of α-secretase (BACE1) through fragment-based drug design
-
(c) Efremov, I. V.; Vajdos, F. F.; Borzilleri, K. A.; Capetta, S.; Chen, H.; Dorff, P. H.; Dutra, J. K.; Goldstein, S. W.; Mansour, M.; McColl, A.; Noell, S.; Oborski, C. E.; O'Connell, T. N.; O'Sullivan, T. J.; Pandit, J.; Wang, H.; Wei, B.; Withka, J. M. Discovery and Optimization of a Novel Spiropyrrolidine Inhibitor of α-Secretase (BACE1) through Fragment-Based Drug Design. J. Med. Chem., 2012, 55, 9069-9088;
-
(2012)
J. Med. Chem.
, vol.55
, pp. 9069-9088
-
-
Efremov, I.V.1
Vajdos, F.F.2
Borzilleri, K.A.3
Capetta, S.4
Chen, H.5
Dorff, P.H.6
Dutra, J.K.7
Goldstein, S.W.8
Mansour, M.9
McColl, A.10
Noell, S.11
Oborski, C.E.12
O'Connell, T.N.13
O'Sullivan, T.J.14
Pandit, J.15
Wang, H.16
Wei, B.17
Withka, J.M.18
-
33
-
-
84901623552
-
Recent progress on routes to spirooxindole systems derived from isatin
-
(e) Xia, M.; Ma, R.-Z. Recent Progress on Routes to Spirooxindole Systems Derived from Isatin. Journal of Heterocyclic Chemistry, 2014, 51, 539-554.
-
(2014)
Journal of Heterocyclic Chemistry
, vol.51
, pp. 539-554
-
-
Xia, M.1
Ma, R.-Z.2
-
34
-
-
0001030407
-
Horsfiline, an oxindole alkaloid from Horsfieldia superb
-
(a) Jossang, A.; Josslang, P.; Hadi, H. A.; Sevenet, T.; Bodo, B. Horsfiline, an oxindole alkaloid from Horsfieldia superb. J. Org. Chem. 1991, 56, 6527-6530;
-
(1991)
J. Org. Chem
, vol.56
, pp. 6527-6530
-
-
Jossang, A.1
Josslang, P.2
Hadi, H.A.3
Sevenet, T.4
Bodo, B.5
-
35
-
-
0000860872
-
Alkaloids of Alstonia Muelleriana
-
(b) Elderfield, R. C.; Gilman, R. E. Alkaloids of Alstonia Muelleriana. Phytochemistry, 1972, 11, 339-343;
-
(1972)
Phytochemistry
, vol.11
, pp. 339-343
-
-
Elderfield, R.C.1
Gilman, R.E.2
-
36
-
-
0003888361
-
-
Springer-Verlag, Berlin
-
(c) Tang, W.; Eisenbrand, G. Chinese Drugs of Plant Origin, Chemistry, Pharmacology and Use in Traditional and Modern Medicine, Springer-Verlag, Berlin, 1992, pp. 997-1002.
-
(1992)
Chinese Drugs of Plant Origin, Chemistry, Pharmacology and use in Traditional and Modern Medicine
, pp. 997-1002
-
-
Tang, W.1
Eisenbrand, G.2
-
37
-
-
33847703663
-
Antiproliferative effects of mitraphylline, a pentacyclic oxindole alkaloid of Uncaria tomentosa on human glioma and neuroblastoma cell lines
-
(d) Garcia Prado, E.; Garcia Gimenez, M. D.; De La Puerta Vazquez, R.; Espartero Sanchez, J. L.; Saenz Rodriguez, M. T. Antiproliferative effects of mitraphylline, a pentacyclic oxindole alkaloid of Uncaria tomentosa on human glioma and neuroblastoma cell lines. Phytomedicine, 2007, 14, 280-284;
-
(2007)
Phytomedicine
, vol.14
, pp. 280-284
-
-
Garcia Prado, E.1
Garcia Gimenez, M.D.2
De La Puerta Vazquez, R.3
Espartero Sanchez, J.L.4
Saenz Rodriguez, M.T.5
-
38
-
-
0033174686
-
Suspected blue canary grass (Phalaris coerulescens) poisoning of horses
-
(e) Colegate, S. M.; Anderton, N.; Edgar, J.; Bourke, C. A.; Oram, R. N. Suspected blue canary grass (Phalaris coerulescens) poisoning of horses. Aust. Vet. J. 1999, 77, 537-538;
-
(1999)
Aust. Vet. J
, vol.77
, pp. 537-538
-
-
Colegate, S.M.1
Anderton, N.2
Edgar, J.3
Bourke, C.A.4
Oram, R.N.5
-
39
-
-
0016604813
-
Gardneria alkaloids-IX structures of chitosenine and three other minor bases: From Gardneria multiflora makino
-
(f) Sakai, S.; Aimi, N.; Yamaguchi, K.; Ohhira, H.; Hori, K.; Haginiwa, J. Gardneria alkaloids-IX structures of chitosenine and three other minor bases: From Gardneria multiflora makino. Tetrahedron Lett., 1975, 16, 715-718;
-
(1975)
Tetrahedron Lett.
, vol.16
, pp. 715-718
-
-
Sakai, S.1
Aimi, N.2
Yamaguchi, K.3
Ohhira, H.4
Hori, K.5
Haginiwa, J.6
-
40
-
-
0029820050
-
Spirotryprostatin B, a novel mammalian cell cycle inhibitor produced by Aspergillus fumigates
-
(i) Cui, C. B.; Kakeya, H.; Osada, H. Spirotryprostatin B, a novel mammalian cell cycle inhibitor produced by Aspergillus fumigates. J. Antibiot., 1996, 49, 832-835;
-
(1996)
J. Antibiot.
, vol.49
, pp. 832-835
-
-
Cui, C.B.1
Kakeya, H.2
Osada, H.3
-
41
-
-
0034647225
-
The asymmetric total synthesis of (+) - and (.) - Spirotryprostatin B
-
(j) Sebahhar, P. R.; Williams, R. M. The Asymmetric Total Synthesis of (+) - and (.) - Spirotryprostatin B. J. Am. Chem. Soc., 2000, 122, 5666-5667.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 5666-5667
-
-
Sebahhar, P.R.1
Williams, R.M.2
-
42
-
-
80051582567
-
Base catalyzed multicomponent synthesis of spiroheterocycles with fused heterosystems
-
(a) Arya, A. K.; Kumar, M. Base catalyzed multicomponent synthesis of spiroheterocycles with fused heterosystems. Mol. Divers., 2011, 15, 781-789;
-
(2011)
Mol. Divers.
, vol.15
, pp. 781-789
-
-
Arya, A.K.1
Kumar, M.2
-
43
-
-
84867258225
-
A domino protocol for the efficient synthesis of structurally diverse benzothiazolylquinoline-2, 5-diones and their spiro analogues
-
(b) Arya, A. K.; Gupta, S. K.; Kumar, M. A domino protocol for the efficient synthesis of structurally diverse benzothiazolylquinoline-2, 5-diones and their spiro analogues. Tetrahedron Lett., 2012, 53, 6035-6038;
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 6035-6038
-
-
Arya, A.K.1
Gupta, S.K.2
Kumar, M.3
-
44
-
-
84864065935
-
Use of SO3H-functionalized halogenfree ionic liquid ([MIM (CH2) 4SO3H] [HSO4]) as efficient promoter for the synthesis of structurally diverse spiroheterocycles
-
(c) Kumar, M.; Sharma, K.; Arya, A. K. Use of SO3H-functionalized halogenfree ionic liquid ([MIM (CH2) 4SO3H] [HSO4]) as efficient promoter for the synthesis of structurally diverse spiroheterocycles. Tetrahedron Lett., 2012, 53, 4604-4608;
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 4604-4608
-
-
Kumar, M.1
Sharma, K.2
Arya, A.K.3
-
45
-
-
79955618726
-
An efficient green chemical approach for the synthesis of structurally diverse spiroheterocycles with fused heterosystems
-
(d) Arya, A. K.; Kumar, M. An efficient green chemical approach for the synthesis of structurally diverse spiroheterocycles with fused heterosystems. Green Chem., 2011, 13, 1332-1338;
-
(2011)
Green Chem.
, vol.13
, pp. 1332-1338
-
-
Arya, A.K.1
Kumar, M.2
-
46
-
-
84893136017
-
An Efficient and environmentally benign four-component domino protocol for synthesis of spirooxindoles spiroannulated with fused heterosystems of privileged heterocycles
-
(e) Khandelwal, S.; Rajawat, A.; Kumar, M. An Efficient and environmentally benign four-component domino protocol for synthesis of spirooxindoles spiroannulated with fused heterosystems of privileged heterocycles. Current Bioactive Compounds, 2013, 09, 203-210;
-
(2013)
Current Bioactive Compounds
, vol.9
, pp. 203-210
-
-
Khandelwal, S.1
Rajawat, A.2
Kumar, M.3
-
47
-
-
84872359679
-
An efficient, ionic liquid mediated onepot, three component sequential synthesis of 3-benzothiazolyl-2-styrylquinazolin-4 (3H)-ones
-
(f) Kumar, M.; Sharma, K., Sharma, D. K.; Arya, A. K. An efficient, ionic liquid mediated onepot, three component sequential synthesis of 3-benzothiazolyl-2-styrylquinazolin-4 (3H)-ones. Tetrahedron Lett., 2013, 54, 878-882;
-
(2013)
Tetrahedron Lett.
, vol.54
, pp. 878-882
-
-
Kumar, M.1
Sharma, K.2
Sharma, D.K.3
Arya, A.K.4
-
48
-
-
84891764800
-
Deep eutectic solvent promoted efficient and environmentally benign four-component domino protocol for synthesis of spirooxindoles
-
(g) Rajawat, A.; Khandelwal, S.; Kumar, M. Deep eutectic solvent promoted efficient and environmentally benign four-component domino protocol for synthesis of spirooxindoles. RSC Adv., 2014, 4, 5105-5112.
-
(2014)
RSC Adv.
, vol.4
, pp. 5105-5112
-
-
Rajawat, A.1
Khandelwal, S.2
Kumar, M.3
-
49
-
-
77956182123
-
Synthesis and antioxidant activity of quinolinobenzothiazinones
-
(a) Kumar, M.; Sharma, K.; Samarth, R. M.; Kumar, A. Synthesis and antioxidant activity of quinolinobenzothiazinones. Eur. J. Med. Chem., 2010, 45, 4467-4472;
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 4467-4472
-
-
Kumar, M.1
Sharma, K.2
Samarth, R.M.3
Kumar, A.4
-
50
-
-
34547760900
-
-
Elsevier: Amsterdam
-
(b) Gupta, R. R.; Kumar, M. "Synthesis, Reactions and Properties of Phenothiazines" in Phenothiazines and 1, 4-Benzothiazines, Chemical and Biomedical Aspect. Elsevier: Amsterdam, 1998, 1-161.
-
(1998)
"Synthesis, Reactions and Properties of Phenothiazines" in Phenothiazines and 1, 4-benzothiazines, Chemical and Biomedical Aspect.
, pp. 1-161
-
-
Gupta, R.R.1
Kumar, M.2
-
51
-
-
33745610170
-
Synthesis of 7-chloro-5-trifluoromethyl/7-fluoro/7-trifluoromethyl-4H-1, 4-benzothiazines as antimicrobial agents
-
(a) Rathore, B. S.; Kumar, M. Synthesis of 7-chloro-5-trifluoromethyl/7-fluoro/7-trifluoromethyl-4H-1, 4-benzothiazines as antimicrobial agents. Bioorg. Med. Chem., 2006, 14, 5678-5682;
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 5678-5682
-
-
Rathore, B.S.1
Kumar, M.2
-
52
-
-
33846880466
-
Synthesis of 7-chloro-9-trifluoromethyl-/7-fluorophenothiazines
-
(b) Rathore, B. S.; Gupta, V.; Gupta, R. R.; Kumar, M. Synthesis of 7-chloro-9-trifluoromethyl-/7-fluorophenothiazines. Heteroatom Chem., 2007, 18, 81-86;
-
(2007)
Heteroatom Chem.
, vol.18
, pp. 81-86
-
-
Rathore, B.S.1
Gupta, V.2
Gupta, R.R.3
Kumar, M.4
-
53
-
-
84928667701
-
L-Proline catalyzed synthesis of structurally diverse 1, 4-dihydropyridines fused with medicinally privileged heterocyclic systems
-
(c) Khandelwal, S.; Rajawat, A.; Kumar, M. L-Proline catalyzed synthesis of structurally diverse 1, 4-dihydropyridines fused with medicinally privileged heterocyclic systems. Current Organocatalysis, 2014, 1. 51-58.
-
(2014)
Current Organocatalysis
, vol.1
, pp. 51-58
-
-
Khandelwal, S.1
Rajawat, A.2
Kumar, M.3
|