Studies on Spiroheterocycles, Part III: Synthesis of Diazaspiroundecanetetraone Derivatives Containing Biologically Active Heterocycles
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A. Behera | R. Behera | A. Pati | R. Pradhan | Manabendra Patra | A. Behera
[1] A. Behera,et al. Studies on Spiroheterocycles, Part II: Heterocyclization of the Spiro Compounds Containing Cyclohexanone and Thiobarbituric Acid with Different Bidentate Nucleophilic Reagents , 2006 .
[2] M. Pedras,et al. Unprecedented chemical structure and biomimetic synthesis of erucalexin, a phytoalexin from the wild crucifer Erucastrum gallicum. , 2006, Organic & biomolecular chemistry.
[3] W. Haq,et al. Synthesis and biological evaluation of 4-thiazolidinone derivatives as potential antimycobacterial agents , 2005 .
[4] S. Kotha,et al. Spiro-annulation of barbituric acid derivatives and its analogs by ring-closing metathesis reaction. , 2005, Bioorganic & medicinal chemistry letters.
[5] M. Kidwai,et al. Ecofriendly synthesis of novel antifungal (thio)barbituric acid derivatives , 2005 .
[6] E. Stevens,et al. Preparation of Nitrogen Heterocycles of Spiro[Furo[2,3‐d]‐Pyrimidine]Pyrimidine Derivatives , 2004 .
[7] M. Ghate,et al. Synthesis of spiro[indolo-1,5-benzodiazepines] from 3-acetyl coumarins for use as possible antianxiety agents , 2004 .
[8] A. Shaabani,et al. Microwave-assisted efficient synthesis of spiro-fused heterocycles under solvent-free conditions , 2004 .
[9] Ruby Singh,et al. MICROWAVE INDUCED DRY-MEDIA SYNTHESIS OF SPIRO[INDOLE-THIAZOLIDINONES/ THIAZINONES] AS POTENTIAL ANTIFUNGAL AND ANTITUBERCULAR AGENTS AND STUDY OF THEIR REACTIONS , 2004 .
[10] A. Shaabani,et al. A reexamination of Biginelli-like multicomponent condensation reaction: One-pot regioselective synthesis of spiro heterobicyclic rings , 2004, Molecular Diversity.
[11] M. Kotera,et al. Synthesis and properties of spiro nucleosides containing the barbituric acid moiety. , 2002, The Journal of organic chemistry.
[12] B. Kokel. A facile entry into a new heterocyclic system: Synthesis of 4,5-annulated-2-dimethylamino-1,3,8,10-tetraaza-spiro[5.5]-1,4-undecadiene-7,9,11(3H,8H,10H)triones , 1996 .
[13] J. P. Williams. Lee's Synopsis of Anesthesia , 1995 .
[14] E. De Clercq,et al. 2',5'-Bis-O-(tert-butyldimethylsilyl)-3'-spiro-5''-(4''-amino-1'',2''- oxathiole-2'',2'-dioxide)pyrimidine (TSAO) nucleoside analogues: highlyselective inhibitors of human immunodeficiency virus type 1 that are targeted at the viral reverse transcriptase. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[15] Takuma Sasaki,et al. Purealidins B and C, new bromotyrosine alkaloids from the okinawan marine sponge psammaplysilla purea , 1991 .
[16] V. Padmavathi,et al. Antimicrobial activity of newly synthesized spiro-pyrimidinetriones, pyrazolidinediones and isoxalidinediones , 1991 .
[17] M. Rajopadhye,et al. Synthesis and antileukemic activity of spiro[indoline‐3,2′‐thiazolidine]‐2,4′‐diones , 1987 .
[18] I. Purkis. Drugs in Anaesthetic Practice , 1980 .
[19] J. Cashman,et al. Lee's Synopsis of anaesthesia , 1973 .
[20] K. Moody,et al. Heterocyclic compounds from alloxan and amines. XII. Tetrahydroquinoxalinespirobarbituric acids and 5-(1-Benzimidazolio)-4-barbiturates from 2-Dialkylaminoanilines , 1970 .
[21] M. Vickers,et al. Drugs in Anaesthetic Practice , 1969 .