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Indian Journal of Chemistry |
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Sect.
B: Organic Chemistry including Medicinal Chemistry |
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VOL. 49B |
NUMBER 4 |
April
2010 |
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CONTENTS
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Papers
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461 |
A novel one pot room
temperature ionic liquid mediated synthesis of 1,5-benzodiazepine ribofuranosides |
A novel one pot ecofriendly synthesis of
7-substituted/7,8-disubstituted-2,2,4-trisubstituted-1-(2′,3′,5′-tri-O-benzoyl-β-d-ribofuranosyl)-2,3-dihydro-1,5-benzodiazepines
has been accomplished stepwise, i.e.
reacting o-phenylenediamine and a ketone in the first step followed by
addition of β-d-ribofuranose-1-bromo-2,3,5-tribenzoate.
The yields (72-90%) of the targeted compounds are excellent. |
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Ashok K Yadav*, Manoj Kumar, Tripti Yadav
& Renuka Jain
Department
of Chemistry, |
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469 |
Efficient microwave activation of hydrotalcite clays
in Michael addition under solvent-free conditions |
Microwave
irradiation has been successfully utilized for the activation of unmodified
hydrotalcite clays, in the Michael addition reaction under solventless
conditions. A plausible mechanism for hydrotalcite catalysis is presented. |
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Sakthivel Vijaikumar & Kasi Pitchumani*
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475 |
One- pot synthesis of
antifungal active 9-substituted-3-aryl-5H,13aH-quinolino [3,2-f][1,2,4]triazolo [4,3-b][1,2,4]triazepines |
The title compounds, 9-substituted-3-aryl-5H,13aH-quinolino[3,2-f][1,2,4]triazolo[4,3-b][1,2,4]triazepines 8, are synthesized from
5-aryl-3,4-diamino-1,2,4-triazoles 5
and 2-chloro-3-formylquinolines 7
using catalytic amount of p-TsOH
and N,N-dimethylformamide as an
energy transfer medium using microwave heating as well as solvent using
oil-bath heating at 80оC affords novel
9-substituted-3-aryl-5H,13aH-quinolino[3,2-f][1,2,4]triazolo[4,3-b][1,2,4]triazepines.
The products are obtained in the good to moderate yields and are in a state
of high purity. |
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Monika Gupta*, Satya
Paul & Rajive Gupta
Department of
Chemistry, |
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482 |
Three component one pot synthesis of β-amino ketones mediated by (bromodimethyl)sulfonium bromide |
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M Shailaja, A Manjula & B Vittal Rao*
Organic Division -
II, Indian Institute of Chemical Technology, |
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Notes |
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487 |
A facile synthesis of N-substituted maleimides |
A
simple and efficient method for the synthesis of N-substituted maleimides from the corresponding maleamic acids
under the phase transfer catalysis has been described. |
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Sunita R Deshpande*, Shailaja P
Maybhate, Anjali P Likhite & Preeti M Chaudhary
Organic
Chemistry Division, National Chemical Laboratory, Pune 411 008, |
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489 |
Purification of lignin
peroxidase from Hexagona tenuis MTCC-1119 and its kinetic properties
in aqueous medium containing miscible organic solvents |
Hexagona tenuis MTCC-1119 secretes lignin peroxidase of molecular wt.48 kDa which retains
50% of its activity in 10% of the water miscible organic solvents acetone,
dioxane, diethyl ether, acetonitrile and dimethyl formamide in aqueous
medium. |
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Meera Yadav*, Sunil Kumar Singh, Kamlesh
Singh Yadav & Kapil Deo Singh Yadav
Department of
Chemistry, |
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495 |
Synthesis of
heneicos-6(Z)-en-11-one, dec-5(Z)-en-1-yl acetate, dec-5(Z)- en-1-yl 3-methylbutanoate (insect
sex pheromones) |
Synthesis of heneicos-6(Z)-en-11-one 1, dec-5(Z)-en-1-yl acetate 2, dec-5(Z)-en-1-yl 3-methylbutanoate 3 has been accomplished by utilizing sodium acetoxyborohydride
generated in situ from sodium
borohydride and acetic acid as the key step for selective
hydroboration-iodination/oxidation. |
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Rani Jindal, Aarti
Devi, Goverdhan L Kad & Jasvinder Singh*
Department of
Chemistry & Centre of Advanced Studies in Chemistry, |
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500 |
Efficient synthesis of
9-aryl-6-(2-fluorophenyl)-1,2,4- |
A simple and highly efficient procedure has been
described for the synthesis of 9-aryl-6-(2-fluoro-phenyl)-1,2,4-
triazolo[4,3-a][1,8]naphthyridines 8 by oxidation of the corresponding aryl aldehyde3-(2-fluorophenyl)-1,8-naphthyridin-2-ylhydrazones
7 with chloramines-T in ethanol
under microwave irradiation. |
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K Mogilaiah*, K Dhanaja,
Department of
Chemistry, |
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505 |
Synthesis and study of chlorosubstituted 4-aroyl and
4-alkoyl-pyrazolines, pyrazoles and their effect on some flowering plants |
Some 4-aroyl and 4-alkoyl-pyrazoline 5a,b from 3-aroyl and 3-alkoylchromanone 4a,b respectively and 4-aroyl and 4-alkoylpyrazole 7a,b from 3-aroyl and
3-alkoylchromone 6a,b
respecttively have been synthesized. Synthesized compounds have been
characterized by analytical and spectral studies. |
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Jaishree D Mahale, S C Manoja, N
G Belsare* & P R Rajput
Department
of Chemistry, Vidyabharati Mahavidyalaya, |
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512 |
Facile synthesis of acyclic
analogues of carbocyclic nucleoside as potential anti-HIV pro-drug |
Microwave induced
montmorillonite K10 clay catalyzed Michael addition of sulphur nucleophile,
(4-oxo-butyl)-dithiocarbamic acid 1 to 4-arylidene-5(4H)-oxazolones
2a-j followed by ring transformation of the resultant Michael adducts 3a-j
which then undergo intramolecular nucleophilic attack on 2 with the simultaneous
cleavage of the oxazolone ring to yield 4a-j in solvent-free
conditions. The control Aldol condensation of compound 4a-j with HCHO
gives compound 5a-j, which upon selective reduction with NaBH4
gives the title compound 6a-j. |
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Ibadur R
Siddiqui*, Pravin K Singh, Vishal Srivastava & J Singh
Laboratory of Green
Technology-Synthesis Division, Department of Chemistry, University of
Allahabad, |
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521 |
Synthesis of some new N-[4-acetyl-4,5- dihydro-5-(1-aryl-5-methyl-1H-1,2,3-triazol-4-yl) -5-methyl-1,3,4-thiadiazol-2-yl]acetamide
derivatives |
The synthesis of some new N-[4-acetyl-4,5-dihydro-5-(1-aryl-
5-methyl-1H-1,2,3-triazol-4-yl)-5-methyl-1,3,4-thiadiazol-2-yl]
acetamide derivatives was reported in paper. |
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Hui-Cheng Wang, Rong-Shan Li,
Hong-Ru Dong & Heng-Shan Dong*
State Key
Laboratory of Applied Organic Chemistry, |
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526 |
Development and assessment of green
synthesis of hydrazides |
An expeditious, solvent-free one
pot method for the preparation of hydrazides from corresponding acids
directly under microwave irradiation was developed and assessed using green
chemistry matrices. |
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Ajoy
Saha, Rajesh Kumar*, Rajendra Kumar & C Devakumar
Division of Agricultural Chemicals, Indian
Agricultural Research Institute, |
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532 |
Synthesis of new isoxazolyl coumarins by eco-friendly
dipyridine cobalt chloride catalyzed Pechmann reaction at ambient temperature |
Dipyridine cobalt chloride is
used as an alternative conventional Lewis acid catalyst in the Pechmann
condensation of isoxazolyl phenols with β-ketoesters leading to the
formation of isoxazolyl coumarins. |
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E Rajanarendar*, Firoz
Pasha Shaik & M Nagi Reddy
Department of
Chemistry, |
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536 |
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Authors for correspondence are indicated by (*) |
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