Characterization of brassinazole, a triazole-type brassinosteroid biosynthesis inhibitor
T. Asami, Y.K. Min, N. Nagata, K.Y. amagishi, S. Takatsuto, S. Fujioka, N. Murofushi, I. Yamaguchi, and S. Yoshida Characterization of brassinazole, a triazole-type brassinosteroid biosynthesis inhibitor Plant Physiol. 123 1 2000 93 100
Bis heterocycles as potential chemotherapeutic agents X. Synthesis of bis(4-arylthiosemicarbazido)-, bis(2-arylamino-1,3,4-thiadiazol-5-yl) and bis(4-aryl-1,2,4-triazolin-3-thione-5-yl)pentanes and related compounds
V.J. Ram, L. Mishra, N.H. Pandey, D.S. Kushwaha, L.A.C. Pieters, and A.J. Vlietinck Bis heterocycles as potential chemotherapeutic agents X. Synthesis of bis(4-arylthiosemicarbazido)-, bis(2-arylamino-1,3,4-thiadiazol-5-yl) and bis(4-aryl-1,2,4-triazolin-3-thione-5-yl)pentanes and related compounds J. Heterocycl. Chem. 27 1990 351
Studies on sulphone derivatives: Preparation and antimicrobial activity of thiosemicarbazides, thiazolidones, triazoles, oxadiazoles and thiadiazoles
P.S. Upadhyay, R.N. Vansdadia, and A.J. Baxi Studies on sulphone derivatives: preparation and antimicrobial activity of thiosemicarbazides, thiazolidones, triazoles, oxadiazoles and thiadiazoles Indian J. Chem. Sect. B. 29 1990 793
Synthese und biologische Wirkungeiniger 1,4-disubstituierter thiosemicarbazide und deren 1,2,4-triazol-5-thion-derivate
N. Ergen, E. lhan, and G. Ötük Synthese und biologische Wirkungeiniger 1,4-disubstituierter thiosemicarbazide und deren 1,2,4-triazol-5-thion-derivate Pharmazie 47 1992 59
Synthesis and antimicrobial evaluation of 3-(4-tert-amino-2-butynyl)thio and alkyl/alkenylthio-4,5-disubstituted-4H-1,2,4-triazoles
Z. Muhi-Eldeen, M. Nadir, N.R. Aljobory, F. Husseen, and S.J. Stohs Synthesis and antimicrobial evaluation of 3-(4-tert-amino-2-butynyl)thio and alkyl/alkenylthio-4,5-disubstituted-4H-1,2,4-triazoles Eur. J. Med. Chem. 26 1991 237
Synthesis of certain thiosemicarbazide and triazole derivatives as potential antimicrobial agents
F.A. Ashour, and S.A. Almazroa Synthesis of certain thiosemicarbazide and triazole derivatives as potential antimicrobial agents Il Farmaco 45 1990 1207
Synthesis of substituted 2,5-bis(1,3,4-oxadiazolyl/thiadiazolyl/1,2,4- triazolyl)indoles and study of their biological activities
S.P. Hiremath, K. Shivaramayya, K.R. Sekhar, and M.G. Purohit Synthesis of substituted 2,5-bis(1,3,4-oxadiazolyl/thiadiazolyl/1,2,4-triazolyl)indoles and study of their biological activities Indian J. Chem. Sect. B. 29 1990 1118
Synthesis of some new hydrazidehydrazones, thiosemicarbazides, thiadiazoles, triazoles and their derivatives as possible antimicrobials
A. Gürsoy,. Demirayak, Z. Cesur, J. Reisch, and G. Ötük Synthesis of some new hydrazidehydrazones, thiosemicarbazides, thiadiazoles, triazoles and their derivatives as possible antimicrobials Pharmazie 45 1990 246
Synthesis of some substituted benzimidazoles with potential antimicrobial activity
I.M. Labouta, A.M.M. Hassan, O.M. Aboulwafa, and O. Kader Synthesis of some substituted benzimidazoles with potential antimicrobial activity Monatsh. Chem. 120 1989 571
Synthesis of 1,2,4-triazole, 1,2,4-triazolo[3,4-b][1,3,4]thiadiazole and 1,2,4-triazolo[3,4-b][1,3,4]thiadiazine derivatives of benzotriazole
S.M. El-Khawass, and N.S. Habib Synthesis of 1,2,4-triazole, 1,2,4-triazolo[3,4-b][1,3,4]thiadiazole and 1,2,4-triazolo[3,4-b][1,3,4] thiadiazine derivatives of benzotriazole J. Heterocycl. Chem. 26 1989 177
Synthesis of some new 5-carboxymethylthio-3,4-disubstituted-triazoles as possible antimicrobial and antiinflammatory agents
N. Ergen, E. lhan, A. Salman, and S. Salman Synthesis of some new 5-carboxymethylthio-3,4-disubstituted-triazoles as possible antimicrobial and antiinflammatory agents J. Fac. Pharm. stanbul 24 1988 37
Synthesis of 4-(5-nitro-2-furfurylidene)amino-3-mercapto-5-(substituted)- 1,2,4-triazoles as possible antibacterial agents
B.S. Holla, B. Kalluraya, and K.R. Sridhar Synthesis of 4-(5-nitro-2-furfurylidene)amino-3-mercapto-5-(substituted)-1,2,4-triazoles as possible antibacterial agents Curr. Sci. 56 1987 236
Synthesis and antibacterial activity of 1-(2,4-dichlorobenzoyl)-4- substituted thiosemicarbazides, 1,2,4-triazoles and their methyl derivatives
B.N. Goswami, J.C.S. Kataky, and J.N. Baruah Synthesis and antibacterial activity of 1-(2,4-dichlorobenzoyl)-4-substituted thiosemicarbazides, 1,2,4-triazoles and their methyl derivatives J. Heterocycl. Chem. 21 1984 1225
Synthesis and antimicrobial testing of certain oxadiazoline and triazole derivatives
E. Hassan, M.I. Al-Ashmawi, and B. Abdel-Fattah Synthesis and antimicrobial testing of certain oxadiazoline and triazole derivatives Pharmazie 38 1983 833
Synthesis of oxadiazolyl-, thiadiazolyl- and triazolylindoles and indolylthiazolidinones
S.P. Hiremath, V.N. Sonar, K.R. Sekhar, and M.G. Purohit Synthesis of oxadiazolyl-, thiadiazolyl- and triazolylindoles and indolylthiazolidinones Indian J. Chem. Sect. B. 28 1989 626
Synthesis and antifungal activity of some new 2-[2-(4′-aryl- 5′-methoxystyryl)-1′,2′,4′-triazol-3′-thio] pyridines [4-aryl-5-[2-[2-(2-pyridyl)vinyl]phenoxy]methyl-1,2,4-triazole-3- thiones]
B.K. Bhattacharya, V.D. Dirk, G. Hoornaert, and S. Sawant Synthesis and antifungal activity of some new 2-[2-(4′-aryl-5′-methoxystyryl)- 1′,2′,4′-triazol-3′-thio]pyridines [4-aryl-5-[2-[2-(2- pyridyl)vinyl]phenoxy]methyl-1,2,4-triazole-3-thiones] Bokin Bobai 12 1984 383
Pyrimidines. VI. Synthesis of 2-methylthio-5-bromopyrimidine-4-carboxylic acid thiosemicarbazides, 3-pyrimidyl-1,2,4-4H-triazoles and 2-arylamino-1,3,4-thiadiazoles
S.C. Bennur, V.B. Jigajinni, and V.V. Badiger Pyrimidines. VI. Synthesis of 2-methylthio-5-bromopyrimidine-4-carboxylic acid thiosemicarbazides, 3-pyrimidyl-1,2,4-4H-triazoles and 2-arylamino-1,3,4-thiadiazoles Rev. Roum. Chim. 21 1976 757
Synthesis and biocidal activity of some substituted oxadiazoles, thiadiazoles and triazoles
C.S. Andotra, and S.K. Sharma Synthesis and biocidal activity of some substituted oxadiazoles, thiadiazoles and triazoles Indian J. Pharm. Sci. 51 1989 107
Studies on acylthiosemicarbazides and related heterocyclic compounds X. Cyclization of 1-(4′-pyridinoyl)-4-aroylthiosemicarbazide derivatives
Z. Zhang, X. Feng, L. Chen, Q. Meng, and D. Gao Studies on acylthiosemicarbazides and related heterocyclic compounds X. Cyclization of 1-(4′-pyridinoyl)-4-aroylthiosemicarbazide derivatives Gaodeng Xuexiao Huaxue Xuebao 10 1989 471
Pyrazine derivatives. XXI. Synthesis and tuberculostatic activity of 4-aryl-1-pyrazinoylthiosemicarbazides and of the products of their cyclization to the derivatives of 1,2,4-triazol-3-thione
W. Rudnicka, H. Foks, M. Janowiec, and Z. Zwolska-Kwiek Pyrazine derivatives. XXI. Synthesis and tuberculostatic activity of 4-aryl-1- pyrazinoylthiosemicarbazides and of the products of their cyclization to the derivatives of 1,2,4-triazol-3-thione Acta Pol. Pharm. 43 1986 523
Reaction of 1,2,4-triazolo-3-thione and some derivatives thereof with isocyanates and isothiocyanates
W. Rudnicka, and J. Sawlewicz Reaction of 1,2,4-triazolo-3-thione and some derivatives thereof with isocyanates and isothiocyanates Acta Pol. Pharm. 35 1978 135
Synthesis and antiviral activity evaluation of some new 6-substituted 3-(1-adamantyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazoles
DOI 10.1016/S0014-827X(01)01189-2, PII S0014827X01011892
M. Kritsanida, A. Mouroutsou, P. Marakos, N. Pouli, S. Papakonstantinou-Garoufalias, C. Pannecouque, M. Witvouw, and E. De Clercq Synthesis and antiviral activity evaluation of some new 6-substituted 3-(1-adamantyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazoles Il Farmaco 57 2002 253 257 (Pubitemid 38365953)
Studies on synthesis and pharmacological activities of 3,6-disubstituted-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles and their dihydro analogues
V. Mathew, J. Keshavayya, V.P. Vaidya, and D. Giles Studies on synthesis and pharmacological activities of 3,6-disubstituted-1,2,4-triazolo[3,4-b]-1,3,4- thiadiazoles and their dihydro analogues Eur. J. Med. Chem. 42 2007 823 840
6-Benzylidenethiazolo[3,2-b]-1,2,4-triazole-5(6H)-ones substituted with ibuprofen: Synthesis, characterization and evaluation of anti-inflammatory activity
B. Tozkoparan, N. Gökhan, G. Aktay, E. Yeilada, and M. Ertan 6-Benzylidenethiazolo[3,2-b]-1,2,4-triazole-5(6H)-ones substituted with ibuprofen: synthesis, characterization and evaluation of anti-inflammatory activity Eur. J. Med. Chem. 35 2000 743 750
Preparation of 5-aryl-3-alkylthio-l,2,4-triazoles and corresponding sulfones with antiinflammatory-analgesic activity
B. Tozkoparan, E. Küpeli, E. Yeilada, and M. Ertan Preparation of 5-aryl-3-alkylthio-l,2,4-triazoles and corresponding sulfones with antiinflammatory-analgesic activity Bioorg. Med. Chem. 15 2007 1808 1814
Synthesis and evaluation of anti-inflammatory, analgesic, ulcerogenic and lipid peroxidation properties of ibuprofen derivatives
M. Amir, and S. Kumar Synthesis and evaluation of anti-inflammatory, analgesic, ulcerogenic and lipid peroxidation properties of ibuprofen derivatives Acta Pharm. 57 2007 31 45
M.S. Langley, and S.P. Clissold Adis International Brotizolam: a Review of Its Pharmacodynamic and Pharmacokinetic Properties, and Therapeutic Efficacy as an Hypnotic, Drugs 1988 104 122
Some 3-thioxo/alkylthio-1,2,4-triazoles with a substituted thiourea moiety as possible antimycobacterials
I. Küükgüzel, S.G. Küükgüzel, S. Rollas, and M. Kiraz Some 3-thioxo/alkylthio-1,2,4-triazoles with a substituted thiourea moiety as possible antimycobacterials Bioorg. Med. Chem. Lett. 11 2001 1703 1707
Synthesis of 3-alkyl(aryl)-4-alkylidenamino-4,5-dihydro-1H-1,2,4-triazol- 5-ones and 3-alkyl-4-alkylamino-4,5-dihydro-1H-1,2,4-triazol-5-ones as antitumor agents
N. Demirba, R. Uurluolu, and A. Demirba Synthesis of 3-alkyl(aryl)-4- alkylidenamino-4,5-dihydro-1H-1,2,4-triazol-5-ones and 3-alkyl-4-alkylamino-4,5- dihydro-1H-1,2,4-triazol-5-ones as antitumor agents Bioorg. Med. Chem. 10 2002 3717 3723
Results of the ATAC (Arimidex, Tamoxifen, Alone or in Combination) trial after completion of 5 years' adjuvant treatment for breast cancer
ATAC Trialists Group J.S.
A. Howell, J. Cuzick, M. Baum, A. Buzdar, M. Dowsett, J.F. Forbes, G. Hoctin-Boes, J. Houghton, G.Y. Locker, J.S. Tobias ATAC Trialists Group Results of the ATAC (Arimidex, Tamoxifen, Alone or in Combination) trial after completion of 5 years' adjuvant treatment for breast cancer Lancet 365 2005 60 62
Synthesis and analgesic activity of some triazoles and triazolothiadiazines
DOI 10.1016/S0014-827X(99)00016-6, PII S0014827X99000166
G. Turan-Zitouni, Z.A. Kaplancikli, K. Erol, and F.S. Killic Synthesis and analgesic activity of some triazoles and triazolothiadiazines Il Farmaco 54 1999 218 223 (Pubitemid 29259824)
Antifungal agents: Mode of action, mechanism of resistance, and correlation of these mechanisms with bacterial resistance
M. Ghannoum, and L.B. Rice Antifungal agents: mode of action, mechanism of resistance, and correlation of these mechanisms with bacterial resistance Clin. Microbiol. Rev. 12 1999 501 517
Further studies in substituted 4H-1,2,4-triazoles for possible hypoglycemic activity
M.Y. Mhasalkar, M.H. Shah, and S.T. Nikam Further studies in substituted 4H-1,2,4-triazoles for possible hypoglycemic activity J. Med. Chem. 14 3 1971 260 262
The mechanism of action of aldolases. III. Schiff base formation with lysine
E. Grazi, P.T. Rowley, T. Cheng, O. Tchola, and B.L. Horecker The mechanism of action of aldolases. III. Schiff base formation with lysine Biochem. Biophys. Res. Commun. 9 1962 38 43
Synthesis and antimicrobial activity of some 5-phenyl-4-substituted amino-3-mercapto (4H)-1,2,4-triazoles
G. Rao, S. Rajasekaran, and M. Attimarad Synthesis and antimicrobial activity of some 5-phenyl-4-substituted amino-3-mercapto (4H)-1,2,4-triazoles Indian J. Pharm. Sci. 62 6 2000 475 477
Synthesis of heterocycles. Part VI. Synthesis and antimicrobial activity of some 4-amino-5-aryl-1,2,4-triazole-3-thiones and their derivatives
N.F. Eweiss, A.A. Bahajaj, and E.A. Elsherbini Synthesis of heterocycles. Part VI. Synthesis and antimicrobial activity of some 4-amino-5-aryl-1,2,4- triazole-3-thiones and their derivatives J. Heterocyclic Chem. 23 5 1986 1451 1458
2,4-Dihydro-3H-1,2,4-triazol-3-ones as anticonvulsant agents
J.M. Kane, B.M. Baron, M.W. Dudley, S.M. Sorensen, M.A. Staeger, and F.P. Miller 2,4-Dihydro-3H-1,2,4-triazol-3-ones as anticonvulsant agents J. Med. Chem. 33 10 1990 2772 2777
(1990)J. Med. Chem., vol.33, Issue.10, pp. 2772-2777
Discriminating behavior of metal ions and ligands with regard to their biological significance
H. Sigel, and D.B. McCormick Discriminating behavior of metal ions and ligands with regard to their biological significance Acc. Chem. Res. 3 1970 201 208
Extension of the "model" approach to the study of coordination chemistry of vit. B12 group compounds
A. Bigotto, G. Costa, G. Mestroni, G. Pellizer, A. Puxeddu, E. Reisenhofer, L. Stefani, and G. Tauzher Extension of the "model" approach to the study of coordination chemistry of vit. B12 group compounds Inorg. Chim. Acta, Rev. 4 1970 41 49
Synthesis of 1,10-dithia-4,7,13,16-tetra-azacyclo-octadecane, 1-aza-4,7-dithiacyclononane, and N, N′-1,2-bis(1-aza-4,7-dithia- cyclononyl)ethane. Structural and solution studies of their silver complexes
A.S. Craig, R. Kataky, R.C. Matthews, D. Parker, G. Ferguson, A. Lough, H. Adams, N. Bailey, and H. Schneider Synthesis of 1,10-dithia-4,7,13,16-tetra- azacyclo-octadecane, 1-aza-4,7-dithiacyclononane, and N, N′-1,2-bis(1-aza- 4,7-dithia-cyclononyl)ethane. Structural and solution studies of their silver complexes J. Chem. Soc., Perkin Trans. 2 1990 1523 1531
Synthesis, X-ray crystal structure, and solution properties of nickel(II) complexes of new 16-membered mixed-donor macrocyclic Schiff base ligand incorporating a pendant alcohol function
A.A. Khandar, and S.A. Hosseini-Yazdi Synthesis, X-ray crystal structure, and solution properties of nickel(II) complexes of new 16-membered mixed-donor macrocyclic Schiff base ligand incorporating a pendant alcohol function Polyhedron 22 11 2003 1481 1487
Synthesis and characterization of the nickel(II) complex of a macrocyclic Schiff base ligand with a single pendant coordinating hydroxyl arm
A.A. Khandar, and S.A. Hosseini-Yazdi Synthesis and characterization of the nickel(II) complex of a macrocyclic Schiff base ligand with a single pendant coordinating hydroxyl arm Aust. J. Chem. 56 12 2003 1255 1257
Copper complexes with new oxaaza-pendant-armed macrocyclic ligands: X-ray crystal structure of a macrocyclic copper(II) complex
M. Vicente, R. Bastida, A. Macias, L. Valencia, C.F.G.C. Geraldes, and C.D. Bronidino Copper complexes with new oxaaza-pendant-armed macrocyclic ligands: X-ray crystal structure of a macrocyclic copper(II) complex Inorg. Chim. Acta 358 4 2005 1141 1150
Synthesis and characterization of some metal complexes with new nitrogen-oxygen donor macrocyclic ligands - X-ray crystal structures of a 26-membered reduced monoprotonated macrocycle and a 20-membered pendant Schiff-base macrocyclic cadmium(II) complex
M. Vicente, C. Lodeiro, H. Adams, R. Bastida, A. Blas, D.E. Fenton, A. Macias, A. Rodríguez, and T. Rodríguez-Blas Synthesis and characterization of some metal complexes with new nitrogen-oxygen donor macrocyclic ligands - X-ray crystal structures of a 26-membered reduced monoprotonated macrocycle and a 20-membered pendant Schiff-base macrocyclic cadmium(II) complex Eur. J. Inorg. Chem. 2000 5 2000 1015 1024
Some general principles for designing electrocatalysts with hydrogenase activity
V. Artero, and M. Fontecave Some general principles for designing electrocatalysts with hydrogenase activity Coord. Chem. Rev. 249 15-16 2005 1518 1535
Carboxyester hydrolysis catalyzed by a novel dicopper(II) complex with an alcohol-pendant macrocycle
S. Li, J. Xia, D. Yang, Y. Xu, D. Li, M. Wu, and W. Tang Carboxyester hydrolysis catalyzed by a novel dicopper(II) complex with an alcohol-pendant macrocycle Inorg. Chem. 41 7 2002 1807 1815
(2002)Inorg. Chem., vol.41, Issue.7, pp. 1807-1815
Applications of polyazamacrocycles with nitrogen-attached pendant arms
K.P. Wainwright Applications of polyazamacrocycles with nitrogen-attached pendant arms A.G. Sykes, Advances in Inorganic Chemistry 52 2001 AcademicPress San Diego 293 334
Complexes of macrocycles with pendant arms as models for biological molecules
J. Costamagna, G. Ferraudi, B. Matsuhiro, M. Campos-Vallette, J. Canales, M. Villagrán, J. Vargas, and M.J. Aguirre Complexes of macrocycles with pendant arms as models for biological molecules Coord. Chem. Rev. 196 1 2000 125 164
A facile synthesis, structure, and antimicrobial evaluation of novel 4-arylhydrazono-5-trifluoromethyl-2,4-dihydropyrazol-3-ones, their N- and N, O-bis-β-d-glucosides
N.S.A.M. Khalil A facile synthesis, structure, and antimicrobial evaluation of novel 4-arylhydrazono-5-trifluoromethyl-2,4-dihydropyrazol-3-ones, their N- and N, O-bis-β-d-glucosides Carbohydr. Res. 344 2009 1654 1659
Antimicrobial evaluation and structure-activity relationship (SAR) of 4-amino-4H-[1,2,4]-triazole-3,5-dithiol and some related 6-substituted-2H-[1,2, 4]triazolo[3,4-b][1,3,4]thiadiazole-3-thiones
N.S.A.M. Khalil, G.A.M.A. Darwish, F.A.A. Mostafa, and N.I. Bassuony Antimicrobial evaluation and structure-activity relationship (SAR) of 4-amino-4H-[1,2,4]-triazole-3,5-dithiol and some related 6-substituted-2H-[1,2, 4]triazolo[3,4-b][1,3,4]thiadiazole-3-thiones Az. J. Pharm. Sci. 37 2008 34 48
Novel simple efficient synthetic approach toward 6-substituted-2H-[1,2,4] triazolo[3,4-b][1,3,4]thiadiazole-3-thiones and first synthesis and biological evaluation of N-and S-β-d-glucosides of the[1,2,4]triazolo [3,4-b][1,3,4]thiadiazole ring system
N.S.A.M. Khalil Novel simple efficient synthetic approach toward 6-substituted-2H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole-3-thiones and first synthesis and biological evaluation of N-and S-β-d-glucosides of the[1,2,4]triazolo [3,4-b][1,3,4]thiadiazole ring system Nucleosides, Nucleotides Nucleic Acids 26 2007 347 359
First synthesis and antimicrobial activity of N- and S-α-l- arabinopyranosyl-1,2,4-triazoles
N.S.A.M. Khalil First synthesis and antimicrobial activity of N- and S-α-l-arabinopyranosyl-1,2,4-triazoles Nucleosides, Nucleotides Nucleic Acids 26 2007 361 377
N- and S-α-l-Arabinopyranosyl[1,2,4]triazolo[3,4-b][1,3,4]thi- adiazoles. First synthesis and biological evaluation
N.S.A.M. Khalil N- and S-α-l-Arabinopyranosyl[1,2,4]triazolo[3,4-b] [1,3,4]thi-adiazoles. First synthesis and biological evaluation Eur. J. Med. Chem. 42 2007 1193 1199
Efficient synthesis, structure, and antimicrobial activity of some novel N- and S-β-d-glucosides of 5-pyridin-3-yl-1,2,4-triazoles
N.S.A.M. Khalil Efficient synthesis, structure, and antimicrobial activity of some novel N- and S-β-d-glucosides of 5-pyridin-3-yl-1,2,4- triazoles Carbohydr. Res. 341 2006 2187 2199
Synthesis of some new 1,3/ or 1,4-bis(glucopyranosyl-1,2,4-triazol-5- ylthio)propanes/or butanes as potential antimicrobial agents
A.A. Abbas, and N.S.A.M. Khalil Synthesis of some new 1,3/ or 1,4-bis(glucopyranosyl-1,2,4-triazol-5-ylthio)propanes/or butanes as potential antimicrobial agents Nucleosides, Nucleotides Nucleic Acids 24 2005 1353 1372
Synthesis of some novel N-ribosyl-1,2,4-triazin-6(1H)-/ones or thiones as potential antibacterial and antifungal chemotherapeutics
N.S.A.M. Khalil Synthesis of some novel N-ribosyl-1,2,4-triazin-6(1H)-/ ones or thiones as potential antibacterial and antifungal chemotherapeutics Nucleosides, Nucleotides Nucleic acids 24 2005 111 120
Synthesis of some novel 6-benzyl(or substituted benzyl)-2-β-d- glucopyranosyl-1,2,4-triazolo[4,3-b][1,2,4]triazines as potential antimicrobial chemotherapeutics
N.S.A.M. Khalil, A.K. Mansour, and M.M. Eid Synthesis of some novel 6-benzyl(or substituted benzyl)-2-β-d-glucopyranosyl-1,2,4-triazolo[4,3-b] [1,2,4]triazines as potential antimicrobial chemotherapeutics Nucleosides, Nucleotides Nucleic Acids 23 2004 1889 1910
Selective synthesis and reactions of 6-substituted-2-β-galactosyl-1, 2,4-triazines of potential anticancer activity
A.K. Mansour, M.M. Eid, and N.S.A.M. Khalil Selective synthesis and reactions of 6-substituted-2-β-galactosyl-1,2,4-triazines of potential anticancer activity Nucleosides, Nucleotides Nucleic Acids 22 2003 21 44
Synthesis of some new 2-α-l-arabinopyranosyl-1,2,4-triazines as potential antitumor chemotherapeutics
A.K. Mansour, M.M. Eid, and N.S.A.M. Khalil Synthesis of some new 2-α-l-arabinopyranosyl-1,2,4-triazines as potential antitumor chemotherapeutics Nucleosides, Nucleotides Nucleic Acids 22 2003 1805 1823
Synthesis of some N-galactosides of 3-aryl-5-benzyl(or substituted benzyl)-1,2,4-triazin-6(1H)-/ones or thiones of expected biological activity
A.K. Mansour, M.M. Eid, and N.S.A.M. Khalil Synthesis of some N-galactosides of 3-aryl-5-benzyl(or substituted benzyl)-1,2,4-triazin-6(1H)-/ ones or thiones of expected biological activity Nucleosides, Nucleotides Nucleic Acids 22 2003 1825 1833
Synthesis and reactions of some new heterocyclic carbohydrazides and related compounds as potential anticancer agents
A.K. Mansour, M.M. Eid, and N.S.A.M. Khalil Synthesis and reactions of some new heterocyclic carbohydrazides and related compounds as potential anticancer agents Molecules 8 2003 744 755
Selective synthesis and structure of 6-arylvinyl-2- and 4-glucosyl-1,2,4-triazines of expected interesting biological activity
A.K. Mansour, Y.A. Ibrahim, and N.S.A.M. Khalil Selective synthesis and structure of 6-arylvinyl-2- and 4-glucosyl-1,2,4-triazines of expected interesting biological activity Nucleosides Nucleotides 18 1999 2265 2283
Efficient route to 20-32 membered macrocyclic crown diamides via ring closing metathesis
Y.A. Ibrahim, H. Behbehani, and N.S. Khalil Efficient route to 20-32 membered macrocyclic crown diamides via ring closing metathesis Tetrahedron 60 2004 8429 8436