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Indian Journal of Chemistry www.niscair.res.in; http://nopr.niscair.res.in
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Sect.
B: Organic Chemistry including Medicinal Chemistry |
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VOL. 49B |
NUMBER 12 |
December
2010 |
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CONTENTS
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Papers
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1637 |
A new quinone from Maesa indica (roxb.)A.dc,
(myrsinaceae) |
A
new benzoquinone, kiritiquinone
2,5-dihydroxy-6-methyl-3-(henicos-16-enyl)-1,4-benzoquinone, has been
isolated from the fruits of Maesa
indica (Roxb.) A.DC. |
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Gina R Kuruvilla, M
Neeraja, A Srikrishna*
G S R Subba Rao, A V
Department of Organic Chemistry, Indian
Institute of Science, |
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1642 |
Synthesis and biological screening of novel
derivatives of 3-(N-substituted carboxamidoethylthio)-(4H)-1,2,4-triazoles |
3-Mercapto-(4H)-1,2,4-triazole has been synthesized
from |
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Anil M
Manikrao*, Ravindra A Fursule,
K
Department
of Pharmaceutical Chemistry, Parul Institute of Pharmacy, Limda, Vadodara 391
760, |
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1648 |
Total synthesis of three
natural products: Decyl 8-hydroxyheptadecanoate, undecyl hexadecanoate and
2,3-dihydroxypropyl hexadecanoate |
First
syntheses of decyl 8-hydroxy-heptadecanoate 1 and undecyl hexadecanoate 2
via utilization of microwave
energy have been achieved and a
new synthesis of 2,3-dihydroxypropyl hexadecanoate 3 has also been accomplished from readily available starting
compound hexadecanol. |
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Department
of Chemistry and Centre for Advanced Studies in Chemistry, |
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Notes |
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1653 |
Aluminium
nitrate as an efficient and reusable catalyst for the three components
one-pot Mannich reaction: Synthesis of β-amino carbonyl compounds |
Three components one-pot Mannich reaction of aromatic
ketones, aromatic aldehydes and aromatic amines has been efficiently
catalysed by recyclable aluminium nitrate at ambient temperature to give
various β-amino carbonyl compounds in high yields. |
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Min Wang*, Yan Liang & Zhiguo Song
College of
Chemistry and Chemical Engineering, |
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1657 |
Quantitative structure
activity relationships for the nematicidal activity of 4-amino-5-substituted aryl-3-mercapto-(4H)-1,2,4-triazoles |
The
relationship between the structure of a series of 4-amino-5-substituted
aryl-3-mercapto-(4H)-1,2,4-triazoles and their nematicidal activity against M. incognita and R. reniformis has been studied using physicochemical parameters
of the molecules. |
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Bijul Lakshman A, R L Gupta* & D Prasad
Division of Agricultural
Chemicals, Division of Nematology, Indian Agricultural Research Institute, |
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1662 |
Synthesis of
benzothiazole appended b-lactams through[2+2]-cycloaddition
reaction |
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Arasampattu S Nagarajan, D Kathirvelan,
M
Pramesh & Boreddy S R Reddy*
Industrial
Chemistry Laboratory, Central Leather Research Institute, Chennai 600 020, |
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1667 |
Synthesis of N-1-(3,5-dimethyl-4-isoxozolyl)-3-(4-aryl-5-thioxo-4,5-dihydro-1-H–1,2,4-triazol–3-yl)propanamides as
possible antitumor agents |
Synthesis
of N-1 (3,
5-dimethyl-4-isoxazolyl)-3-(4-aryl-5-thioxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)-propanamides 7 have been accomplished from 4-amino-3,5-dimethylisoxazole |
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M Nagi Reddy
& E Rajanarendar*
Department
of Chemistry, |
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1671 |
Synthesis and bioactivity evaluation of pyrazolone derivatives |
A series of 3-methyl pyrazolone derivatives have been
synthesized and characterized. All the compounds have shown significant
analgesic and anti inflammatory activity. |
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Department
of Pharmaceutical Chemistry, Himalayan Pharmacy Institute, Majhitar, East
Sikkim 737 136, |
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1675 |
Studies of antimicrobial activity of picryl amino
pyridine N-oxides |
Biologically active picryl amino pyridines and their
N-oxide have been successfully synthesized and screened for their
antimicrobial potency to set up the structure activity relationships and
found to possess better antibacterial activity than antifungal activity. |
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1678 |
High atom
efficient and environment-friendly preparation of herbicides bromoxynil and
ioxynil |
High
atom efficient and environment-friendly preparation of herbicides bromoxynil and
ioxynil using bromide/bromate and iodide/iodate couple as halogenating
reagent in water at room temperature is described. |
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Girdhar Joshi & Rajendra D
Patil
Central
Salt & Marine Chemicals Research Institute, (CSIR), G. B. Marg, |
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1681 |
Annual Index |
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Authors for correspondence are indicated by (*) |
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