Azabenzomorphane and Related Compounds. VII. Synthesis of 1, 2, 3, 4, 5, 6-Hexahydro-2, 6-methanobenzo [d][1, 3] diazocine Derivatives
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1 1 2 3 4 5 6 Complex craniofacial changes in blind cave-dwelling fish are mediated by genetically symmetric 7 and asymmetric loci 8 9 Joshua B. Gross, Amanda J. Krutzler and Brian M. Carlson 10 11 Department of Biological Sciences, University of Cincinnati, Cincinnati, Ohio 45221 12 13 14 15 16 17 18 19 20 21 22 23 Genetics: Early Online, published on February 4, 2014 as 10.1534/genetics.114.1...
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6-Carbethoxy-5-(3'-bromophenyl)-3-aryl-2-cyclohexenones 2a-j were obtained from the1-Aryl-3-(3'-bromophenyl)-2-propene-1-ones 1a-j by Micheal addition of ethyl acetoacetate, followed by internal Claisen condensation. Reaction of 2a-j with hydrazine hydrate afforded the corresponding 6-Aryl-4-(3'-bromophenyl)-3-oxo-2,3a,4,5-tetrahydro-2H-indazoles 3a-j. The structures of newly synthesized compou...
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8 9 A comparison was made between the composition of the recalcitrant organic matter (ROM) 10 isolated from a sandy forest soil as revealed by microwave assisted extractions and/or 11 hydrolyses and by usual pyrolysis techniques. Successive microwave irradiation treatments 12 were performed in H2O, 0.1 and 1 M HCl and 0.1 and 1 M KOH. At each step of the 13 treatment the insoluble residue was e...
متن کاملSynthesis and Leishmanicidal Activity of 1-[5-(5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl]-4-benzoylepiperazines
A series of (5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl derivatives 6a–6e have been synthesized and screened for in vitro anti-leishmanial activity against the promastigote form of L. major. The structure of Schiff bases were confirmed by 1H NMR, IR. Screening results indicate that all of the designed and synthesized final compounds (6a-6e) significantly reduced the viability of promastigotes ...
متن کاملSynthesis and Leishmanicidal Activity of 1-[5-(5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl]-4-benzoylepiperazines
A series of (5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl derivatives 6a–6e have been synthesized and screened for in vitro anti-leishmanial activity against the promastigote form of L. major. The structure of Schiff bases were confirmed by 1H NMR, IR. Screening results indicate that all of the designed and synthesized final compounds (6a-6e) significantly reduced the viability of promastigotes ...
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ژورنال
عنوان ژورنال: Chemical and Pharmaceutical Bulletin
سال: 1965
ISSN: 0009-2363,1347-5223
DOI: 10.1248/cpb.13.1220