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CONTENTS
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Rapid Communications
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2523
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A new protocol for synthesis of a,b-unsaturated
ketones using zirconium tetrachloride under microwave irradiation
IPC:
Int.Cl.7 C 07 C
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Utpal Bora, Anil Saikia & Romesh C
Boruah*
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Papers
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2527
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A study on the
reactivity of 1,3-dimethyl-2,6-diphenyl-4-piperidone : Synthesis of some
novel heterocycles
IPC: Int.Cl.7 C 07 D
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Some interesting
heterocycles, viz.: tetrahydropyridine, diazepanone, oxazepanone,
pyridoindole, thiazolopyridine,
furanylmethylenepiperidone, pyridopyrimidone and
pyridopyrimidinethione are prepared from piperidin-4-one by exploiting
ketomethylene functionality using microwave, ultrasound and conventional
methods.
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V Padmavathi*, T V Ramana Reddy,
K Audisesha
Reddy, A Padmaja &
D Bhaskar Reddy
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2532
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Synthesis and
anti-inflammatory, analgesic, ulcerogenic and lipid peroxidation activities
of 3,5-dimethyl pyrazoles, 3-methyl pyrazol-5-ones and 3,5-disubstituted
pyrazolines
IPC: Int.Cl.7 C 07 D
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Pyrazole derivatives of
diclofenac, ibuprofen, flurbiprofen and 2,4-dichlorophenoxy acetic acid have
been synthesized with the aim of reducing their ulcerogenic activity.
Moreover, pyrazoline derivatives of ibuprofen have also been synthesized.
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Mohd Amir* &
Shikha Kumar
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2538
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Beibersteneolide-a
and -b: Two new sesquiterpene lactones from Achillea beiberstenii
IPC: Int.Cl.7 C 07 D
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Two new
sesquiterpene lactones obtained from Achillea
beiberstenii have been characterized as 3a, 9b- diacetoxy- 1b, 10-epoxy
5(4)-en-germacran -6b, 12-olide,
named as beibersteneolide-a 1, and
4, 9b-dihydroxy-2(1),
6(5), 11(13) triene-guaian7a, 12-olide,
designated as beibersteneolide-b 2.
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Tawfeq A
Al-Howiriny , Jaber S Mossa &
Bahar Ahmed*
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2545
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Condensation of
reactive phenols with aromatic 1,2-diketones: A single step protocol for
synthesis of benzo-fused g-lactones
IPC: Int.Cl.7 C 07 C
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Condensation of
certain reactive phenols with 1,2-diketones under acid/Lewis acid catalysis
affords benzofused g-lactones in
reasonable yields.
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Sabir H
Mashraqui*, Mamta B Patil, Hitesh D Mistry, Mohamed Ashraf &
Subramanian Sundaram
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2550
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Synthesis and
characterization of di(p-fluorobenzyl)tin
bis(heteroaromatic carboxylate) and crystal structure of di(p-fluorobenzyl)tin
bis(3-pyridinecarboxylate)
IPC: Int.Cl.7 C 07
D
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Reaction of di(p-fluorobenzyl)tin oxide
with heteroaromatic carboxylic acid in 1:2 stoichiometry
yields compounds of the type (4-F-Bz)3Sn(OOCR)2
[R=3-pyridinyl 1,
4-pyridinyl 2, 2-pyridinyl 3, 2-indolyl 4, 2-furanyl 5,
2-thiophenyl 6, 3-indolyl 7, 3-indolmethyl 8]. These compounds have been characterized by
elemental analysis, IR, 1H and 119Sn NMR spectra. The crystal and molecular structure of compound 1 has been determined by X-ray single
crystal diffraction.
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Han DongYin*, Qi
Bao Wang & Sheng Cai Xue
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2555
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Polymer-bound
cationic Rh(I) phosphine catalyst for homogeneous asymmetric hydrogenation
IPC: Int.Cl.7 C 07 D
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Facile synthesis
of polymer bound Rh(I) phosphine catalyst for homogeneous asymmetric
hydrogenation is described. Polymer
bound Pyrphos Rh(I) complex catalyses hydrogenation of prochiral Z-a-acetamido cinnamic acid to
S-N-acetyl phenyl alanine with 76% ee. The polymer bound catalyst is cleanly
separated from the product by membrane osmodialysis.
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Nirmal Koshti*, Shubhangi Naik & Bharat Parab
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2560
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Improved
synthesis of an energetic material, 1,3,3-trinitroazetidine (TNAZ) exploiting
2-iodoxy benzoic acid (IBX) as an oxidising agent
IPC: Int.Cl.7 C 07 D
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The synthesis and characterisation of a powerful strained ring
energetic compound which is of considerable interest to military agency, has
been discussed. Most of the effort for producing the next generation of
energetic materials is currently centered around the production of TNAZ. The
advent of this new high energy explosive presents the possibility of
increased performance with reduced sensitivity.
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Alok Singh,
Nirmala Sikder & Arun K Sikder*
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2564
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Single crystal
XRD structural elucidation of
1-oxopyridinium-2-thioacetic acid
IPC: Int.Cl.7 C 07 D
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Sudalaiandi Kumaresan*, Palani Ramadevi, Balasingh
Ravindran Durainayagam & Rosa Walsh
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2569
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Michael addition
of active methylene compounds to a,bunsaturated
sulfones
IPC: Int.Cl.7 C 07 D
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The Michael
addition of dimethyl malonate and ethyl cyanoacetate to a,b-unsaturated
sulfones in the presence of Triton-B and K2CO3 is
studied.
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V Padmavathi*, D R C Venkata Subbaiah,
A Balaiah, B Chandra Obula Reddy & A
Padmaja |
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2575 |
Synthesis of isoflavones containing naturally
occurring substitution pattern by oxidative rearrangement of
respective flavanones using thallium(III) p-tosylate
IPC: Int.Cl.7 C 07
D |
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Om V Singh*, M Muthukrishnan &
M Sunderavadivelu |
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2582 |
Design, synthesis and characterisation of a
novel anticancer prodrug having antiproliferative activity against
prostrate tumour
IPC: Int.Cl.7 C 07
C |
5'-O-Curcuminyl-diglycinoyl-DNA had
antiproliferative activity against prostrate tumor
derived DU145 cells. It acts by hybridisation with target telomerase
sequence. |
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Satyendra
Mishra, Snehlata Tripathi, Roli Mishra & Krishna Misra*
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2589
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Rapid and
convenient synthetic strategy for
2-amino-4-aryl-5-aryl-sulfonyl thiazoles
IPC: Int.Cl.7 C 07 D
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A convenient one
pot synthetic strategy for 2-amino-4-aryl-5-aryl sulfonyl thiazoles has been
first time introduced.
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V E Bhingolikar,
S R Mahalle, S P Bondge &
R A Mane*
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Notes
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2594
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Synthesis and
biological screening of some new novel indole derivatives
IPC: Int.Cl.7 C 07 D
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Synthesis of some novel indole derivatives has been undertaken by
the reaction of 1,4-benzoquinone with ethyl-b-(arylamino)-crotonates in the presence of nitrogen atmosphere or
in the absence of nitrogen atmosphere.
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D S Mehta, K H
Sikotra & V H Shah*
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2598
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Base induced
carbon-nitrogen (C=N) double bond migration in Schiff bases
IPC: Int.Cl.7 C 07 C
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Various Schiff bases are prepared to study
base induced carbon-nitrogen double bond migrations. Schiff bases derived
from aliphatic aldehydes display highest selectivity. Hydrolysis of the
resulting rearranged Schiff base provides an entry to make amines from
aldehydes.
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B Gangadasu, P
Narender, B China Raju* &
V Jayathirtha
Rao
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2601
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Reaction of
2'-hydroxy-5'-acetamido chalcones with dimethyl sulfoxide-iodine,
pyridine-mercuric (II) acetate and triethanolamine
IPC: Int.Cl.7 C 07 D
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Reaction of 2'-hydroxy-5'-acetamido chalcones with catalytic
amount of iodine in DMSO affords flavone, molar amount of mercuric acetate in
pyridine gives aurones while with phenylhydrazine and hydrazine hydrate gives
pyrazoline in triethanolamine medium.
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Nitin N Agrawal*
& P A Soni
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2604
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Two dimeric
flavonoids from Bauhinia purpurea
IPC: Int.Cl.7 C 07 D
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Bauhinia purpurea leaves yield two new
dimeric flavonoids namely, bis [3¢,4¢-dihydroxy-6-methoxy-7,8-furano-5¢,6¢-monomethylallyloxy]-5-C-5-biflavonyl 1 and (4¢-hydroxy-7-methyl-3-C-a-l-rhamnopyranosyl)-5-C-5-(4¢-hydroxy-7-methyl-3-C-a-glucopyranosyl)
biflavonoid 2 with protein
precipitating capacity 214.4 and
199.24 mgBSA/g,
respectively.
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SurabhiYadav
& Brijesh K Bhadoria*
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2608
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A facile
synthesis of 1-hydroxy-5-chloro-benzo[f][2,7]naphthyridines
IPC: Int.Cl.7 C 07 D
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Synthesis of the
titled compounds from 2-chloro-3-formyl
quinolines is reported.
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N Sampathkumar,
S Thiruvaranga Ramalingam & S P Rajendran*
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2611
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Wolff
rearrangement of Nα-
Boc-/Z-protected aminodiazoketones to the corresponding β-amino acids under microwave
irradiation
IPC: Int.Cl.7 C 07 C
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The Wolff
rearrangement of Na-Boc-/Z-protected aminodiazoketones assisted by microwave
irradiation is described. All the resulting b-amino acids have
been isolated in good yield and purity.
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X= Boc-/Z-
group
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Kantharaju,
Basanagoud S Patil & Vommina V Suresh Babu*
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2614
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Synthesis and antimicrobial activity of some
3-alkyl-
4-(arylmethyleneamino)-4,5-dihydro-1H-1,2,4-triazol-5-ones
IPC: Int.Cl.7 C 07 D
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Eight new ethyl Nı-(3-methyl-4-arylmethyleneamino-4,5-dihydro-1H-1,2,4-triazolyl-5-one)acetates 2 and Nı - (3-methyl-4-arylmethyleneamino-4, 5-dihydro-1H-1,2,4-triazolyl-5-one)acetylhydrazines
3 have been synthesized. The
compounds show some antimicrobial activities.
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Bahittin Kahveci*, Olcay Bekircan &
Şengül Alpay Karaoğlu
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Announcements
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2618
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Second International Symposium On Green/
Sustainable Chemistry
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2619
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Annual Index
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Authors for correspondence are indicated by (*)
IPC: International Patent Classification
Int. Cl7.: International
Classification, 7th Edition, 1999
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