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Indian Journal of
Chemistry |
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Sect. B: Organic Chemistry
including Medicinal Chemistry |
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VOL. 47B |
NUMBER 12 |
December
2008 |
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CONTENTS
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Papers
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1851 |
Synthesis of a stable, storable and
differentially protected acyclic precursor of d-amicetose and its conversion to 4-O-benzyl-protected d-amicetose |
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Indrapal Singh Aidhen* & |
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1858 |
Regioselective reaction: Synthesis of
novel Mannich bases derived from
3-(4,6-disubstituted-2-thiomethylpyrimidyl)-4-amino-5-mercapto-1,2-4-triazoles
and their antimicrobial properties |
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Lingappa B, Girisha K S, Balakrishna
Kalluraya*,
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1865 |
Radermachol and naphthoquinone
derivatives from Tecomella undulata:
Complete 1H and |
Petroleum ether extract of the heartwood of Tecomella undulata affords
radermachol, an unusual rare pigment and |
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1 |
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Pahup Singh*, Poonam Khandelwal,
Noriyuki Hara, Teigo Asai & Yoshinori Fujimoto |
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1871 |
Tin(lV)
catalyzed one-pot synthesis of |
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1876 |
Synthesis
of quinazolinone analogues using sodium perborate as catalyst |
An environmentally
benign approach for the quinazolinone synthesis employing sodium perborate
(SPB) as a selective catalyst is described.
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Mazaahir Kidwai*
& Priya |
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1882 |
Quantitative Structure Activity
Relationship study for the nematicidal activity of O,O-diaryl O-n-propyl phosphorothionates |
The
relationship between the structure of a series of O,O-diaryl O-n-propyl phosphorothionates and their
nematicidal activity against M.
incognita and R. reniformis have been studied using
physicochemical parameters of the molecules. |
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R L Gupta |
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1886 |
Cycloaddition
of 6-hydroxy-2,6 dimethylcyclo-hexa-2,4-dienone: A stereoselective entry into
functionalized bicyclo[2.2.2]octanes and a novel 1,2-migration of methyl
group |
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Vishwakarma Singh*, Girish Chandra &
Shaikh M Mobin
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1892 |
Synthesis of some novel
ethoxyphthalimide derivatives of
pyrazolo[3,4-c]pyrazoles |
Some 6-N-ethoxyphthalimido-4-methyl-3-(4-substituted
phenyl)- 2-thiocarbamoyl-3,3a-dihydropyrazolo[3,4-c]pyrazoles
6a-d and |
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Chirag Sharma, Bhawana Thadhaney, Gangotri
Pemawat & G L Talesara* |
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Notes
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1898 |
Chemical
constituents of Limnophila indica |
Isolation and structural elucidation of two novel
flavonoids, 5,6-dihydroxy-7,8,4'-trimethoxyflavone 1 and 5,2'-dihydroxy-8,3',4'-trimethoxyflavone 2, together with three known
compounds, 5-hydroxy-7,2'-dimethoxy flavone 3, 5,2'-dihydroxy-7,8-dimethoxyflavone 4, and b-sitosterol 5 from the aerial parts and roots of Limnophila indica have been reported. |
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G Brahmachari*, S K Jash, A Gangopadhyay, S Sarkar, |
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1903 |
Synthesis of N-(substituted
benzyl)-2- (3′,5′-dimethyl-4′-hydroxyphenyl)acetamides |
The
chemical synthesis of a series of D-arabinofuranosyl-(1,5)-D-arabinofuranoside disaccharides incorporating
4-deoxy-4-thioarabinose is described. |
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B |
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1906 |
Effect of aniline in
methanol and benzene mixture – An ultrasonic study |
Sound velocity, density and viscosity values have been measured at 303 K in the ternary system of aniline + methanol + benzene. The results are interpreted in terms of molecular interaction between the components of the mixtures. |
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L Palaniappan* & R Thiyagarajan |
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1910 |
An investigation leading to
preparation of tetrahydro-quinazoline derivatives involving ureidoalkylation
and a-amidoalkylation reactions |
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V K Pandey*, Mukesh, Anilesh Kumar & Noopur Trivedi |
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1915 |
Synthesis
of dibenzo -18- crown -6 ether containing pyrimidine derivatives |
The
strategy employed for the synthesis of new macromolecules containing
pyrimidine moiety involved the acetylation of dibenzo-18-crown-6 (1)
to yield 4,4¢-
diacetyl derivative of dibenzo-18-crown-6 (2), which was further
reacted with different aldehydes to give the corresponding chalcone 3.
Reaction of chalcones 3 with guanidine hydrochloride give the target molecules 4.
The structures of synthesized compounds have been established on the basis of
spectroscopic data. |
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4 |
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M B Deshmukh*,
K N Alasundkar, S M Salunkhe , D K Salunkhe , S A Sankpal, D
R Patil & P V Anbhule |
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Annual Index
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1918 |
Author
Index |
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1923 |
Keyword
Index |
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1930 |
Announcement
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Authors for correspondence are indicated by (*)
Annual Index 2008
Author Index
Abbasoglu Rza 90
Abdula M M 1451
Abdullah S T 619
Adapa S R 1243
Adhikari A V 144, 439
Ahmed B 945
Aidhen I S 1851
Akbari J D 477
Alam M M 1243
Alam M S 619, 740
Alasundkar K N 1915
Ali I 740
Ali M 619
Alphonse I 942
Aminkhani A 1151
Amutha C 276
Anas S 1063
Anbhule V 792
Anbhule P V 1915
Anebouselvy K 449
Annamalai T 163
Ansari F Y 1759
Ansari S H 619
Arabindoo B 963
Arumugam P 1084
Asai T 1865
Asha S 1726
Awasthi P 1291
Babu S N N 297
Babu V V S 910, 917
Banerjee S 1108
Bapna A 1096
Barua A 938
Baruah A 1568
Basu B 1701
Bezbaruah B 1605
Bharathan A 1145
Bhat S V 1308
Bhavsar A M 579, 1135
Bhusari K P 586, 1559
B in H H 773
Biswas S 927
Bodhankar S L 903
Borhade S R 1549
Brahmachari G 1898
Britto S J 942
Bruni G 903
Cao Hong 166
Chakraborty B 485
Chandra G 1886
Chandrashekhar C 753
Chanotiya C S 1249
Chaturvedi S C 957
Chhetri M S 485
Coumar M S 903
Dabholkar V V 1759
Dandale A S 613
Dandia A 427
Das A T 1447
Das N 1555
Das P J 938, 1568
Das S 1701
Dash D K 460
Dash S 259
Deb A C 1120
Deepak D 1744
Deniz N G 1407
Desai K R 1695
Desai N C 579, 1135
Deshmukh M B 792, 1915
Deshmukh S P 613
Deshpande N 927
Devi C S 592
Devi Nirada 153
Devi S K C 1145
Dhandapani P S 276
Dhanwad R 144
Din A S E 1451
Dong H-S 171
D ong Z X 773
Dravyakar B R 1559
Dubey P K 1443
Duggar R 1298
Dwivedi A D 136
Francis M 1145
Fujimoto Y 1865
Gaidhane P K 1260
Ganapaty S 1243
Ganga V B 1071
Gangal S 601
Gangopadhyay A 1898
Ganguly M 153
Gao C 481
George V 1726
Ghosh D 1298
Girisha K S 1858
Gokhale G D 310
Gorai D 1898
Gupta M 1739
Gupta M M 470
Gupta N 1303
Gupta R 434, 1303
Gupta R L 1882
Gupta Rajive 1739
Gupta Raman 1739
Haldar A G M 1260
Hamid H 619
Hara N 1865
Hariharakrishnan V S 1281
Hariprasad K 1281
Hatzade K M 1260
He Y 1600
Hu Haobin 166
Huang K 1435
Huang S 1435
Huo G-Y 171
Ibis C 1407
Iinuma M 952
Ingle V N 1260
Ismail T 740
J M Rao 623
Jadhav S D 792
Jagdale A R 1091
Jagtap S S 792
Jain R 117
Jain Shubhi 136
Jana S 1430
Jash S K 1898
Jayashankara V P 1160
Jeyaraman R 129, 411
Jian Yufeng 166
Jindal D P 903
Jirovetz L 1731
Jose B 1731
Joshi H S 477
Jyothi D 630
Kabiri R 1151
Kad Goverdhan L 155
Kadam V J 721, 1587
Kalita R 1605
Kalluraya B 1858
Kamat S P 1597
Kanaujia A 1298
Kantharaju 917
Karabasanagouda T 144
Karim M 892, 1605
Katade S 927
Kathiravan S 1117
Katiyar C K 1298
Kaur Irvinder 155
Kaur J 291
Kaur Jasamrit 155
Kaur R 470
Kawade D P 1559
Khade A B 626
Khan I A 740
Khan S 945
Khan Shabana I 97
Khandelwal P 427, 1865
Khare A 1744
Khare N K 1744, 1748
Khedekar P B 586, 1559
Khorassani S M H 1151
Kidwai M 1876
Koshti S M 329
Kotha S 1120
Kotra V 1243
Krishna N 325
Kumar A 1910
Kumar B N H 963
Kumar H M S 740
Kumar N 748
Kumar N D M 1443
Kumar N R 1243
Kumar N V 764
Kumar P R 1414
Kumar P Vijaya 106
Kumar S 1277, 1463
Kumar V 1739
Kumari N S 439, 1858
Kumar M M K 325
Kundu P 1402
Laskar S 1898
Li J T 283
Lin Z P 283
Lingappa B 1858
Liu C T 283
Liu Jianxin 166
Liu W 1600
Ma Z-T 171
Maddry J A 1748
Madhavan S 1113
Magerramov A 90
Maghsoodlou M T 1151
Mahajan R K 1291
Mahammed K A
Mahammed K A 575, 1160
Mahesh K 1707, 1713
Mahulikar P P 329
Maiti G 1402
Maity T K 460
Malasoni R 470
Mallya S 626
Mammen D 932
Mandal B 1701
Mandour A H 1451
Manju S L 1145, 1726
Manjula K 597
Marandi G 1151
Marihal S C 626
Mashelkar U C 764
Masoodi M H 945
Massarelli P 903
Master Hoshang E 97
Mathela C S 1249
Mayekar S A 1254, 1397, 1438
Medhi C 892, 1605
Mehta K B 477
Menezes J C 1597
Mishra B K 259
Misra R 966
Mistry B D 1695
Mobin S M 1886
Mohamed Shafi P 1731
Mohan A V N 1707
Mohan G 112, 781
Mohan R 721
Mohandass P 1447
More D H 329
Mukesh 1910
Mukhopadhyay T 163
Mulwad V V 1254, 1397, 1438
Mundada A S 721
Muralidhar P 325
Murthy P S K 575
Murugesh K 460
Muthusubramanian S 276, 305
Nagaraj A 315, 319, 787, 1154
Nagasathya R 1447
Nagle P S 329
Naidu A 1443
Namitharan K 305
Nandakumar K 903
Narendra N 917
Narute A S 586
Nayyar A 117
Nema A 606
Ojha S 1096
Padalia R C 1249
Padmaja A 734, 1713
Padmavathi V 734, 1707
Paira M 966, 1430
Paknikar S K 1597
Palaniappan L 1906
Pandey R 470
Pandey V K 1910
Parameshwarappa G 144
Paranjape T B 310
Paraskar A S 1091
Parthasarathy T 1871
Paschapur M S 626
Pasha M A 597, 1160
Patel B V 885
Patel H 473
Patel H S 885
Patel J A 1695
Patel K C 885
Patel S 259
Pathak S J 477
Pathak V N 434, 1303
Patil D R 792, 1915
Pattan S R 626
Paul K 291
Paul S 1739
Pawar Y A 329
Payani T 1713
Pemawat G 1892
Periasamy M 1080
Perumal P T 1084
Phalgune U 927
Pheko T 159
Philip S K 1145
Ponnuswamy S 129, 411
Poojari Krishna A 97
Pradeep N S 1726
Prajapati Y 473
Prakasam T 963
Prasad S H 630
Praveen B 781
Priya 1876
Purohit S S 626
Qazi G N 740
Qazi N A 740
Radhakrishnan K V 1063
Radhalakshmi T 1707
Raghavaiah P 592
Raghu M 315, 1572, 1578
Raghubir Ram 136
Raghunathan R 1117
Raghuvanshi R S 1735
Rai M 778
Rai N S 1858
Rajalingam D 460
Rajan R 1063
Rajanarendar E 112, 781, 1284, 1591,1753
Rajasekharan K N 1145, 1726
Rajeswar Rao V 106
Raju B C 623, 1903
Raju K M 575
Rama C S 721
Ramana D V 963
Ramesh D 753
Ramesh P 1447
Rameshwar N 1871
Rami Reddy A S 112, 1591, 1753
RamReddy A 1871
Ramu K 1284
Rane M D 1308
Rangappa K S 297
Ranu B C 1108
Rao B K 592
Rao B V 1281
Rao D V 325
Rao E K 781
Rao G V 1762
Rao H S P 272
Rao M S 781, 1423
Rao V R 759
Rasal V P 626
Rauf A 601
Ravindra K C 1271
Reddy A S R 781, 1284
Reddy C S 315, 319, 787, 1154
Reddy K M 759
Reddy P V V P 1443
Reji T F A F 1145
Reynolds R C 1748
Roy S 1108
Roy S C 966, 1430
Saghatforoush L 1151
Sahoo P K 957
Sahu Sagarika 259
Sahu Sandhyamayee 259
Salunkhe D K 1915
Salunkhe S M 792, 1915
Samant S D 310
Sandhu J S 1463
Sanjeeva Reddy Ch 1572, 1578
Sankpal S A 792, 1915
Saravanan S 276, 305
Sarika C 1063
Sarkar S 1898
Sarma R L 892, 1605
Sastry B S 325
Satishkumar S 1080
Satyamurthi N 1851
Sawant S D 740
Sawy E R E 1451
Saxena A K 579
Selvaraj S J 942
Sen J P 1583
Sengupta P 460
Shafi S 740
Shah M D 579, 1135
Shaik F P 1284, 1591, 1753
Shaker K H 1451
Shanmugam P 1113
Sharma A K 903
Sharma C 1892
Sharma L K 1277
Sharma R 957
Sharma S 601
Shen T 1600
S heng H H 773
Shirodkar P Y 1587
Shrivastava P K 1555
Shrivastava S K 1555
Shukla D K 463
Shukla Rakesh 136
Siddhaye B M 1597
Sidhu A 778
Singh A N 1281
Singh G S 159
Singh J 460
Singh Jasvinder 155
Singh K N 1545, 1735
Singh M S 767
Singh P 291, 427, 1865
Singh P P 740
Singh Pallavi 767
Singh Pratibha 767
Singh R 903
Singh R K P 1277
Singh S K 1545
Singh V 1886
Sireesha B 592
Sivasubramanian S 276
Solankee A 473
Solankee P 473
Solankee S 473
Somani R R 1587
Sonar J P 329
Sonawane A E 329
Sondhi Sham M 136
Sonu 155
Sonwane S K 633
Sreejalekshmi K G 1145
Srikrishna A 449, 1414, 1423
Srinivas A 787
Srinivasan P S 963
Srivastava S D 463, 606, 633, 1583
Srivastava S K 606, 633
Sudalai A 1091
Sudheer K 734
Sun G 1600
Sun L 481
Suresh C H 1071
Suresh E 1071
Syam S 1308
Taile V S 1260
Talesara G L 1096, 1892
Tandel R C 932
Tang K 1435
Thadhaney B 1892
Thirupathaiah A 1762
Thiyagarajan R 1906
Thomas K K 1145
Thomas P S 1298
Tiwari A 1249
Trivedi N 1910
Uygur Yaprak 90
Vagdevi H M 1271
Vaidya V P 753, 1271
Vaithiyanathan V 1113
Varala R 1243
Varma R L 1071
Varshney B 434
Vattipalli Ramya 1587
Venkataramanarao R 910
Venkateswara Rao G 163
Venkatraj M 129, 411
Verma A 1555
Verma M 1545
Vijaya kumar P 759
Vineel B G 1443
Viswambharan B 1113
Waghmode S B 1549
Wagle S 439
Wakharkar R 927
Wang L 952
Wang M 952
Wang Z T 952
Wei Y 481
Xu L S 952
Yadav A K 748
Yadav P 1277
Yeligar V C 460
Yi J 1435
Zhang C F 952
Zhang M 952
Zheng S 1600
Zheng Xudong 166
Zhou W 481
Keyword Index
Ab initio 1605, 892
Ab initio calculations 90
Absolute configuration 1744
Acetamides 1903
Acetylation 1739, 1915
Acetylenic esters 1151
Acid chlorides 597
Acid hydrazide 1438
Acorones 1423
Acylpyrimidines 291
Adrenergic blockers 1587
Adrenergic blocking agents 903
Adrenergic receptor binding 903
Alcohols 1739
Aldehyde 938, 1091, 1108, 1762
Aldehyde synthesis 485
Aldose reductase activity 957
Aldoximes 259
Alkali 473
Alkenylbenzothiazole 601
Alkyl halides 439
Alkylation 892
Alkylbenzothiazole 601
Alstonia scholaris 1298
Alstonoside 1298
Aluminium trichloride 283
Amide 315, 1851
Amine 291, 1572, 1739
Amino coumarin 1397
Amino methylcarbamates 920
Amino nitriles 1572
Amino thiophenols 1753
Amino-4-phenyl-1,3-thiazole 633
Aminoacetophenone 778
Aminobenzonitrile 1876
Aminobenzothiazole 1583
Aminocoumarin 1254
Aminoethanethiol 1713
Aminoethanol 1713
Aminothiazole 1145
Analgesic 136
Analgesic activity 439, 1271
Anti rotamer 411
Antibacterial 144,297, 463,
Antibacterial activity 579, 606, 781, 787, 932,
1135, 1284, 1397, 1695, 1726
Anticancer 106
Anti-cancer activity 291, 460
Anticonvulsant 626
Antifungal 144, 463, 1695
Antifungal activity 1284
Antifungal activity 606, 740, 781, 787, 932
A ntihepatotoxic activity 945
Antihypertensive 626
Antihypertensive activity 764
Anti-inflammatory 136, 144, 439
Anti-inflammatory activity 1243
Anti-inflammatory effect 1451
Antimicrobial activity 159,477, 633, 748, 753, 927,
1243, 1254, 1271, 1303, 1583
Antimicrobial peptide 297
Antimony trichloride 1402
Antipyretic 619
Antitubercular 106
Antitubercular activity 297, 586, 1695
Antiviral 106
Aphrodisiac 619
Apocynaceae 1298
Aromatic aldehydes 1397
Aromatization 1568
Aryl amines 613
Aryl-1,3-thiazoles 144
Arylidenes 633
Aryl-N-[1-methyl-2-(2/4-chlorophenyl)]ethyl nitrones 276
Aryloxypropanolamines 1587
Asclepiadaceae 1744
Asymmetric synthesis 1308
Azetidinone 159, 606, 1695
Aziridine ring 892
Azo compounds 329
Azomethine ylide 1113, 1117
Barbituric acid 1120
Baylis-Hillman adduct 1113
Benzal-4-acetylanilines 778
Benzaldehydes 778
Benzimidazole 957, 787, 1096, 1154, 1443
Benzo[ b ]pyran 1108
Benzodiazepines 1463
Benzodioxin derived macrocycle 1071
Benzofuran 1451
Benzooxazole 1254
Benzopyran-2-one 106, 759
Benzothiaphene 586
Benzothiazepine 473
Benzothiazole 1254
Benzothiazolyl carbamides 613
Benzotriazole 463
Benzoyl glycine 932
Benzyloxy-3,5-dimethylphenylacetate 1903
Berberidaceae 1600
Berberis pachycantha 945
B ibenzyl derivative 952
BiCl 3 1762
Bicyclo[2.2.2]octane 1886
Bicyclo[3.2.2]nona-6,8-diene 90
Biginelli condensation 434
Biginelli reaction 1871
Biological activity 1260
Bis(indolyl) methane 623, 1402
Bisthiazole 1726
Boat conformation 129, 411
Boc-amino acids 920
Bromoalkoxyphthalimide 1096
Bromopyridines 1701
Burseran 1430
13 CNMR 305
Calculated parameters 1906
Calix[4]bis(spirodienone) 1071
Calogenin 1744
Carbamate 613, 1545
Carbazoles 606
Carbonyl compound 259, 623, 1572
Carbostyril 1759
Carvone 1414
Catalysis 966
Catalyst 1091, 1549
Catalyst free 1084
Cathartic 619
Cationic 297
Cell count 460
Ceric ammonium nitrate 315, 966
Chalcones 927, 1915
Changyediyuine 1600
Characterization 1435
Chelated 1898
Chemical shift prediction 1865
Chemical transformation 1731
Chloramines-T 1707
Chloro-5,6-dihydro-2 H -pyran derivatives 1762
Chloroacetyl chloride 310, 1583
Chlorooxime 740
Chromones 1260
Claisen rearrangement 1423
Claisen-Schmidt condensation 1303
Classical pathway 97
C lerodane diterpenoid glucoside 166
Clerodendrum phlomidis L 470
C-N coupling 1701
C-O coupling 1701
Complement inhibition 97
Computational chemistry 1865
Concomitant synthesis 920
Condensation 112
Condensed pyrimidine 136
Conjugate addition 283
C onstituent 166
Controlled potential electrolysis 1277
Conventional 606
Copolyesters 885
Copper 1091
Criegee fragmentation 449
Cross metathesis 1063
Crystal 592
Crystal structure 1407
Cu catalyst 1701
CuCl 2 .2H 2 O-Conc. HCl 434
Curtius rearrangement 910, 920
Cyanobacterium 1597
Cyclic a,ß-unsaturated ketones 630
Cycloaddition 1113, 1886
Cyclohexa-2,4-dienone 1886
Cyclohexyl heteroaryl sulphide 305
C ytotoxic activity 952
Cytotoxicity 1145
Daunomycin 1605
Deacetylation 1260
Dehydrocubebin 1430
Dendrobium grati o sissimum 952
Dendrodoine 1145
D engraol A 952
D engraol B 952
Deoximation 259
Deoxy prazole 1443
De-oxygenative cyclization 1591
Deoxysugar 1851
Deprotection 938
DFT calculations 90
Diacetates 938
Diamines 427
Dianion 767
Diaryl-1,4-pentadien-3-one 283
Diaryl-bis-imidazoquinoxaline 1281
Dibenzo 18-crown-6 containing pyrimidine 1915
Dibenzo-18-crown-6 1915
Dicarbonyl compound 966, 1120
Diels-Alder reaction 1886
Diethylethoxymethylene malonate 1555
Dihydropyridine 626, 1568
Dihydropyrimidinone 434, 1871
Dimethyl dicoumarin 1447
Dimethyl malonate 734
Dimidone 1759
Dioxadiazaphosphatridecine 767
Dioxazaphosphadecines 767
Dipolar cycloaddition 1707
Dipole 1117
Dispiropyrrolidine 1117
Dithiocarbamate 1545
Dithiolane 272
Dithiole 272
DNA 892, 1605
Double Michael addition 734
Drug targeting 721
Drug-resistant TB 117
Drug-sensitive TB 117
Dynamic NMR 1151
Eco-friendly 155
Electrochemical oxidation 1277
Electrophilic addition 90
Electrophilic substitution 623
Elsholtzia bodinieri Van't 166
Enamines 291
Enaminones 966
Enantiospecific synthesis 449, 1414
Energy barrier 411
Epoxides 1430
Essential oil 1731
Esterification 597
Etheration 1435
Ethyl benzalcyanoacetate 778
Ethyl cyanoacetate 734, 778
Ethylcholesta-5,22 E ,25-triene-3ß-ol 470
Extreme drug-resistant TB 117
Fatty acids 601
Fe-modified K10 310
First order 963
Flavone 1898
Flavonoid 1898
Force field 1605
Formaldehyde 112
Four-component coupling 1578
Friedel-Craft reaction 153, 310
Friedlander heteroannulation 1160
Friedlander reaction 753
Furan 481
Furanosyl-(1?6)-ß- d -glucopyranoside 773
Furobenzopyrone 1451
Gallium(III) chloride 1463
Glacial acetic acid 473
Glucopyranosyl bromide 1260
Glucosides 1260
Glucosylation 1260
Glycosyl inhibitors 1748
Green chemical protocol 276
Green chemistry 434, 1277
Green procedure 1108
Green synthesis 792
Grignard reaction 171
Grindstone chemistry 434, 1303
Grubb's catalyst 1063
Guanidine hydrochloride 1915
1 HNMR 305, 411
Haemolysis 97
Hantzsch 1084
Hantzsch 1,4-dihydropyridines 1735
Hantzsch coumarin 1447
Heck reaction 1549
Hemedesmus indicus 1744
Heptadecenoic acid 155
Himachalenes 1414
HL-60 cell 952
HMBC study 159
HMQC study 159
Homologation 1851
Homopropargylic alcohols 1762
Hyatella cribriformis 325
Hydrated form 592
Hydrogen 592
Hydrolysis 1308
Hydroxy presilphiperfolene 1249
Hydroxy-14 b -methyl-7-oxopodocarp-5-en-13-
(19 a -hydroxy-19,22,22-trimethylheptyl)-
22-O-( b - d -gluco-pyranosyl)-(4 ® 1)
b - d -glucopyranoside 619
Hydroxylamine hydrochloride 740
Hydroxymoyl chloride 740
Hypertension 903
Hypoglycemic activity 1555
Imide-like intermediate 963
Iminothiazolidinone 1397
Indanone 1597
Indole 283, 481, 623, 1402
Indolyl chalcone 1303
Inhibition 460
Insect growth regulator 1291
Interacalation 1605
Intermedeol 1249
Intramolecular ene-reaction 1414
Inula cuspidata 1249
Iodine 1438
Ionic liquid 1108
IR 748, 885
Irradiation 315
Isocyanides 1151
Isoflavone apioglucosides 1298
Isoniazid 1892
Isopropenylnaphtho[2,3-b]furan-4,9-quinone 1865
Isoquinoline alkaloids 945
Isothiocyanato coumarins 1438
Isoxazole 473, 1096
Isoxazoline derivatives 1559
Isoxazolyl 1,3,5-benzoxadiazocine-4-thiones 1753
Isoxazolyl acids 1284
Isoxazolyl benzimidazoles 1284
Isoxazolyl indazoles 1591
Isoxazolyl-1,3-benzoxazines 112
Juvenile hormone 1291
Ketene acetal 272
Keto derivative 1744
Ketones 1463, 1762
Ketoximes 259
Knoevenagel condensation 630
Labiatae 166
Lactone 942, 1851
Lactosyl isocyanate 613
Lapachol 427
Lapachone 427
Lead carbonate 575
Ligand-free conditions 1701
Limnophila indica 1898
Linear free energy relationship 579, 1135
Lipases 1308
Liquid crystalline property 932
Lupeol ester 470
Malononitrile 734
Mandelic acids 1243
Mannich base 1858
Marine alkaloid 1145
Marine sponge 325
Measured parameters 1906
Meldrum ¢ s acid 1120
Meloidogyne incognita 1882
Melonol 1308
Metal chelators 291
Metathesis 1120
Methanol 171
Methyl-3-aryl-2-( Z -styrylsulfonyl)acrylate 734
Methylcoumarin 1597
Methylene ketones 1160
Methylene-bis-2,4-dihydrochromeno[4,3- c ]pyrazoles 319
Methylene-bis-4-oxo-1,4-dihydrochromeno-
[4,3- c ]pyrazoles 319
Michael addition 481, 1555
Microwave 315, 1545
Microwave assisted synthesis 606
Microwave irradiation 153, 575, 601,
1154, 1762, 1876
Microwave -assisted organic synthesis 630
Migration 1886
Mitomycin A 892
Mitomycin C 892
Mole fraction 1906
Molecular interaction 1906
Monoterpenoids 329
Montmorillonite K10 153, 310
Mosquito larvicidal test 781
Mullilam 1731
Multi-component condensation 1108
Multicomponent reaction 1091
Multi-drug resistant TB 117
Multifid oside A 773
Multifid oside B 773
Mycobacterial arabinogalactan 1748
N-(2-hydroxymethylphenyl)salicylideneimine 767
N,N'-bis(salicylidene)- trans -1,2-diaminocyclohexane 767
N,S-Substituted nitrodiene 1407
N 1 , N 5 -Diacetyl 129
N 1 , N 5 -Diacyltetrahydro-1,5-benzodiazepin-2-one 129
N 1 , N 5 -Dibenzoyl 129
NaH 1713
Naphtho[2,1- b ]furan 1271
Naphthofuran 753
Naphthofuropyridine 753
Nardal 163
Nardostachys jatamansi 163
N -chloroacetyl- r -2, c -6-diarylpiperidin-4-one 411
N -Chlorosuccinimide 740
Nematicidal activity 787, 1882
Neolignan glycoside 773
Nickel ferrite 1549
Ninhydrin 1113
Nitrile imines 1707
Nitrile oxides 1707
NMR 129, 885
NMR spectra 411, 748
Non-cytotoxic 97
Nonsteroidal anti-inflammatory drugs 1559
Nostoc commune 1597
N- Phenyl- N- cyclohexyl-a-chloronitrone 485
N -protected amino acid/peptide isoxazoles 781
o-Aminoaryl ketones 1160
o -Ethyl dithiocarbonate 1443
Olefins 1549
One-pot conversion 1578
One-pot synthesis 1591
One-pot three-component condensation 1572
o -Phenylenediamines 1463
Orchidaceae 952
Organophosprous compounds 1882
Orthoester 1154
Ovine bactenecin5 297
Oxadiazole 439, 460, 579
Oxazoline 1713
Oxidation 1568
Oxime 259, 740
Oximinoketones 963
Oxo-azetidines 633, 1135
Oxo-thiazolidines 1135
Pachycanthine 945
Palladium 1549
Passive cutaneous anaphylaxis 1281
Pentafluorophenyl carbamate 910
Peptide isocyanate 910
Peptidyl urea 910, 920
Periploca calophylla 1744
Phase transfer catalyst 792, 1735
Phellandral 1731
Phenol 575, 597, 1739
Phenoxypropanolamines 903
Phenyloxazol-5-one 932
Phosphorothionates 1882
Phosphorous pentasulphide 601
Photobiological activity 1451
Photochemical process 259
Phthalimides 1243
Phthalimidoxyethyl bromide 1892
Piperazine derivatives 1407
Platinum electrode 1277
p -Menthane-1,2,7-triol 1731
Polyhydroquinolines 1084, 1578
Polyhydroxy ketone 619
Potasium osmate (VI) dihydrate 1080
Potassium carbonate 792
Predictable metabolism 721
Proline 1113
Protection 938
Pteris multifida Poir 773
Pterosins 1597
p - tert -Butylcalix[8]arene 1435
p - tert -Butylcalix[8]arene ether derivatives 1435
p -TsOH 319, 1572
Pyramidalization 90
Pyranopyridine 764
Pyrazol-3-one derivatives 1555
Pyrazole 927, 1096, 1260
Pyrazolidine 1451
Pyrazoline 1303
Pyrazolo[3,4- c ]pyrazoles 1892
Pyrazolo[3,4- d ]pyrimidines 477
Pyrazolone 1120, 1451
Pyridine 764, 1438
Pyrido[3,2 -b ][1,4]benzothiazine 748
Pyrimidin-5-ones 759
Pyrimidine 792, 1096, 1858
QSAR 579, 586, 957, 1882, 1135, 1559
Quaternary ammonium bromate 1568
Quinazolin-4-ones 1876
Quinazolinone 1254
Quinoline 1160
Quinoxaline 439
Racemic dihydroxylation 1080
Radermachol 1865
Radical cyclization 1430
Rational drug design 721
R -Carvone 449
RCM reaction 1423
Re-cyclable heterogeneous catalyst 1739
Reduction 1753
Regioisomers 427
Regioselective synthesis 319
Regioselectivity 90
Retrometabolism 721
Reusable catalyst 597
Ribofuranosides 748
Ring closure 112, 1753
Ring opening metathesis 1063
Ring-substituted quinolines 117
Room temperature 1084
Rotylenchulus reniformis 1882
Rumex maritimus 619
Rutaceae 1731
Salicylaldehydes 112
Sanguisorba 1600
Sarcosine 1113
Scalarane sesterterpenes 325
Schiff base 1753, 1858
Secoiridoid glucoside 1298
Second order Beckmann rearrangements 963
Seed germination 932
Selenadiazoles 305
Semiempirical MO calculation 129, 411
Sesquiterpene 1414, 1423
Sesquiterpene aldehyde 163
Silica supported zinc chloride 1739
Silymarin 945
Simplified Cadogan's synthesis 1591
SmCl 3 1713
SN 2 reaction 485
Sodium perborate 1876
Soft drugs 721
Solid phase 315
Solid state reaction 938, 1284
Solid state synthesis 276
Solid-phase synthesis 153
Solvent extraction 1277
Solvent free 434, 1463
Solvent-free condition 597, 1084, 1871
Solventless organic reactions 276
Solvent-system 1876
Spectral data 473
Spiro[4.5]decane 1423
Spiro-annulation 1120
Spirocycles 1120
Spiroiminolactones 1151
Spirothiazolidinone 787
Spontaneous motor activity 1910
Stereoselectivity 90
Substituted arylhydrazines 1555
Substituted benzoic acids 963
Substituted benzothiazole 613
Substituted benzyl amines 1903
Substituted pyridines 1568
Substituted-3-methylcyclohexenones 630
Sulphides 1443
Superoxide 1545
Superoxide ion 1735
Surface templated process 259
Surfactant 938
Syn rotamer 411
Syn -1,2-diols 1080
Synthesis 136, 171, 1435, 1587
TBAB 1443
TEA 1443
Tecomella undulata 1865
Terpene glycoside 619
tert -Butyl bromide 575
tert -Butyl ethers 575
Tetrahydroisoquinolines 1903
Tetrahydroquinazolines 1910
Tetrahydrothieno[3,2 -c ]pyridine 97
Tetramethyl- n -octadac-13-en-3,4,6,7,8,11-hexol-12-one 619
Tetratriacontanol 470
Tetronic acid 1120
TFA 1443
Thaps-8-en-5-ol 449
Thermogravimetric analysis 885
Thiadiazine 106
Thiadiazole 305, 463, 579, 1438
Thiazine 1759
Thiazole analog 1145
Thiazole 144, 759
Thiazolidinone 1254, 1397, 1583, 1695
Thiazoline 1713
Thiazolo pyrimidone 759
Thiazolo[4,5 -d ]pyrimidines 477
Thioarabinofuranosyl disaccharides 1748
Thioether 1407
Thiofuranoses 1748
Thioglycolic acid 1583
Thiohydatoin 1254
Thiomorpholine 1407
Thiosemicarbazide 592, 1892
Thrope-Zielger reaction 753
Thymol 329, 1249
Thymyl isobutyrate 1249
Thymyl isovalerate 1249
Tiliacora acuminata 942
Tin(IV) chloride 1871
TiO 2 597
Titanocene(III) chloride 1430
Tosylmethyl isocyanide 1707
Total synthesis 155
Transesterification 1308
trans -Stilbenes 1080
Triazabicyclic molecules 1063
Triazine 885
Triazole 106, 171, 579, 1271,
1281, 1858
Triazoline-3,5-diones 1063
Triazolothiadiazines 1271
Triazolothiadiazole 1271
Trihydroxy-7,3 ' -dioxy-8,4 ' -neolignan-
4- O -ß- d - apiofuranosyl-(1?6) -ß- d - glucopyranoside 773
Trimethylsilyl cyanide 1572
Tris(indolyl)alkane 1402
Triterpene ester 470
Triterpenoids 1600
Triton B 734
Tröger base 1080
TsOH 623
Tuberculosis 117, 1748
Tumor weight 460
Ultrasonication 283, 920
Ultrasound 155
Unsaturated aldehyde 1402
Unsaturated sulfone 1707
Ureidoalkylation 1910
Vanillin 903
Variable temperature 411
Wittig reaction 1447
X-ray diffraction 305, 592
Yttrium triflate 481
Zanthoxylum rhetsa 1731
ZrCl 4 catalyst 1578
ZrOCl 2 .8H 2 O 1154