Sale of Surplus Property Request for Quote
Commodity(s) Available: See attached list of 224 items Enter supplier name and address here

Vendor Candidate:

Submit Proposal To:
Tom Petocz Procurement Manager RTI International
RTI Compound procurement@lgp-iraq.org
Date of Issue of RFQ: Date Questions Due From Sellers Date Proposal Due: Method of Submittal: Attachments TO RFQ:
All bidders are responsible to carefully review each attachment and follow any instructions that may be relevant to this purchase.
May 8, 2011 NA 15:00 pm on May 11, 2011
Respond via e-mail w/ attached document in MS Word. Purchaser must quote all line items and/or services in order to be considered for evaluation. 1. Section A Commodity Specifications 2. Section B Bid and Sale Conditions
Section "A" Commodity Specifications (Page 1 of 6)

SectionA

Commodity Specifications
Line Item 43 Manufacturer Kitchen Aide Tefal Crafft Crafft Nokia Shownic Strong LG Strong Philips LG Cosonic Shownic Strong LG Strong LG Strong LG Strong LG LG Strong SHOWNIC Open Star Denka LG LG Strong Strong Strong LG LG Arclik Strong OSN Daewoo Strong LG OSN Strong Shownic Strong Model Serial Number N/A WTW3548426 N/A 2100044136 024V8G 401010802 024V8G 358067010352497 TLCR32Q3700 1005R32Q370494 SRT4622XII XII46220911760349 29FU6RST5 911NLVE004039 4665X X46651001332637 DVP3360K98 KX1A1012877584 32LF15RTA 001KCWC2P897 N/A 121910090706845 TLCR32Q3700 1005R32Q4630031002752 29FESRGE 701LPGE000087 SRT 4620X X46200705012081 21FU1RG 707SYJR4620030653686 21FS4RGEDC 703LPLQ4642061001624 RT-1FE30VE 601ETRP000526 32LF15RTA 909SRAV5B4620070400889 TC21MAX45 G157A7L775T004180 TORMD03201H 09C3201091200045 LS32LCD 1031808101055 29FESRGE 610LPLQ000032 29FU3RG - TG 905LPMP003115 SRT 4620X X46200707015185 4620X X4620060830947 29FS7RL 709SYZZ1G749 MH6548FR 907TAHQSRT 4620X X46200707004033 KSC - B275NSS 004842 DTD-29G5MT GT35DM0113 SRT 4620X X46200707004171 29FD7RGETR 704LPUH000118 N/A 004866 N/A 4820070504911 TLCR32Q3700 1005R32Q370503 SRT 4620X X46200707004038 Description KitchenAide Toaster Sandwich Grill A.C Crafft Window A.C Crafft Window Nokia Mobile Phone TV LCD Shownic Settalite Receiver Strong TV 29" 29FU6RST5 Settalite Receiver Strong DVD Player TV LG 32" DVD Player (Cosonic) TV LCD Shownic 32' RECIVER Strong 4600 T.V LG Electronics receiver Strong T.V LG 21'' RECIVER Stron LG T.V 19' Receiver Strong TV LG Flatron T.V LCD LG 32' Receiver Strong T.V SHOWNIC 21" TV LCD 32 TV Denka LCD 32 T.V LG Electronics T.V LG Super Slim Settalite Receiver Strong Receiver Strong Receiver Strong TV LG LG Microwaive Oven Refregirate Arcilk Settalite Receiver Strong Receiver OSN TV DAEWOO Settalite Receiver Strong LG T.v 29' Receiver OSN Receiver Strong TV LCD 32' Shownic Settalite Receiver Strong Quantity 1 Bid $
Section "A" Commodity Specifications (Page 2 of 6)

Line Item 92

Manufacturer LG OSN Strong Nokia Nokia Nokia Nokia Nokia Nokia Nokia Nokia General Sunwood Nokia LG LG Dolphin Gibson Gibson LG Strong LG Funsat Nokia Nokia Nokia General Nokia LG Kelon Nokia Nokia Nokia Sunwood LG LG Sunwood Canon LG LG Senao IBM Maixma HP LG Senae LG Maixma Canon
Model Serial Number 29FU6RST5 002NLKL000285 KSCB275NSS 004797 SRT 4620X X- 3500c - GDR165D 0503010534 SD1203 - N/A 0602TK00305 LWN2463BAQ 208KA01113 N/A 310275790 GWHH24GNAWGK95301365 GWHH24GNAWGK95301270 21F- A2R9E/TY 707LPTV000905 SRT 4620X X46200707002977 29FE5RGE 610LPQN000172 SS-GDR165D 359756000620488 MH6548FRR 907TAVY00119 N/A 355515019524766 SDMS - 2344B 601TACX00075 MS-192W 404TA02710 SDLide 100 KDHB30934 GP08NU20 006HKJU051012 GP08NU6B 004HKJU335084 EUB-368 EXT - AB1 66DE100129915 F2410 CN03JBJ1QC GP08NU20 006HKPV051040 N/A 06A231319 GP08NU20 006HKNME091121911 Lide 25 VYC039968

Section "A" Commodity Specifications (Page 4 of 6)

Line Item 190

Manufacturer Maixma Denka Maxima Senae Samsung Maxima Maxima Denka Nobel Nobel Maxima Denka Denka Denka Maxima Maxima Maxima Concord OSN LG Denka Philips Strong Concord LG Shownic OSN OSN Strong TAG Denka Denka SANYO LG KDM Maxima Maixma Maixma LG HATESHE LG Kelon N/A UGUR TAG Denka Royal Commercial Samsung
Model Serial Number 850 E09115565 BA137RDA E090851863 N/A 06A231323 940BX HA19HCGP111078D 1200 E090851864 MATR32AFFIC 004902 NWD1559RRNWD1559RRMA800 E0901157419 IRI82PLE 7010603105900 IRI82PLE 7010603106231 TR32AFFIC 7021003094395 MA800 E090805513 MA800 E091157342 MA800 E090847878 BC - 95 WK0095090721HCONC001801 KSC - B275NSS 004843 21F- A2R9E/TY 708ETCG010579 N/A 7235170 DVP3360K98 KX1A1012877590 SRT 4620X X46200707004036 N/A 40462567 32LFI5RTA 001KCZR73541 TLCR32Q3700 1005R32X370070 N/A 004814 N/A N/A 1102228778000903500067 BA137RDA 7235037 BA137RDA 7872147 SR-23355okww30200062 DG9411P 508SHBS000597 HMA800 EEE091156256 MS - 2344B 503TAGH01599 HS010471705280412 MS - 192W 404TA03061 N/A 945039028067260325 N/A M21200000100053470245 UGURUUS374D MN/A 7235209 PC-R96FR 0708047270 S -4ACW300152Y
Description UPS Maxima 850VA Refregirate DENKA BA137RDA UPS Maxima 1200 Wirless senao system Samsung 19' monitor UPS MAXIMA 1200 UPS Maxima 1200 Water Cooler Denka TR32AFFIC Water Cooler Nobel Water Cooler Nobel UPS Maxima 1200 Water Cooler Denka Water Cooler Denka Water Cooler Denka TR32AFFIC UPS Maxima 1200 UPS Maxima 1200 UPS Maxima 1200 Refrigerator Concord BC - 95 Receiver OSN TV LG 21' 21F- A2R9E/TY Refrigerator DENKA DVD Player Philips Settalite Receiver Strong SRT 4620X Frezzer Concord 16FT T.V LG 32' 32LFI5RTA TV LCD Shownic Receiver OSN Receiver OSN Receiver Strong Refrigrater TAG Refregirator Denka Refrigrater Denka Refrigreater SANYO DVD,VCD, CD Player LG DG9411P Sheader Machine UPS Maxima 1200 UPS Maxima 850VA UPS Maxima 850VA Microwaive Oven LG Wave Dom Refrigrater Hitachi Microwaive Oven LG Wave Dom Refrigreater Kelon Big Refrigreate 18 FTwith Class Door Refrigreator UGURUUS374DTKL Refrigrater TAG Refrigrater Denka Refrigartor 6 FT Shradder Machine Commercial S- 800 Refrigrater Samsung

Section "A" Commodity Specifications (Page 5 of 6)

Line Item 203 204

Manufacturer Concord TAG General Denka N/A Denka Concord Arcelik Westing House Denka TAG N/A Vestel

Model ET-700 GDR165D

BA137RDA N/A N/A N/A N/A N/A N/A
Serial Number CCXD1102229083000975900346 Approximate Quantity
Description Refrigrater Con cord 6 FT ET-700 Refrigrater TAG Refrigrater General GDR165D Refregriate DENKA Sheadder Machine Refregirator Denka BA137RDA Fridge, Concord 18 FT Washing Machine Dryer Machine Refrigrater Denka 5 FT refrigerater TAG Enternal Air cooler Refrigreater Barbecue Gril

Quantity 1 2

Section "A" Commodity Specifications (Page 6 of 6)

Line Item 223 224

Manufacturer
Serial Number Approximate Quantity Approximate Quantity Approximate Quantity Approximate Quantity
Approximate Quantity Approximate Quantity Approximate Approximate Approximate Approximate Approximate Approximate Quantity Quantity Quantity Quantity Quantity Quantity
Approximate Quantity Approximate Quantity Approximate Quantity
Description Electrical Plastic Box Light Bulb Ceiling Light Plastic Window Change over 1600A Change over 100A Fire Extinguisher Leather Bag Mashering Machine Desk Signe Electrical Bulb Rat Poison Iron Shelf Wooden Shelf Bunk Bed External Fan Bed Mattress Wooden Counter with Mirror Sheets
Quantity Count 744 Total Bid $
Above list subject to Final inventory. Be aware that a Final list will be distributed at the site visit. By signing the Final Section "A" attachment, the bidder confirms he has a complete understanding of the specifications and fully intends to purchase items as indicated within the Final listed information. I further certify that I am not an RTI employee, and have not been for at least six (6) months, and am not purchasing this property for or on behalf of any RTI employee.

Firm Name

Street Address

City/Country

Phone No.

Fax No.

Section B

Bid and Sale Conditions

BSC-1 DESCRIPTION: The equipment, materials or personal property identified in this RFQ is being sold in an As Is condition. RTI International (hereinafter identified as RTI) does not warrant the condition, operation or functionality of this equipment for any particular use or for any subsequent marketability. Offers submitted by the PURCHASER must indicate a unit price for each item they wish to bid on in this RFQ. RTI reserves the right to award the sale of individual items to multiple companies or all items to one company as deemed to be in the best interest of RTI. RTI makes no stipulations concerning the PURCHASERS use of this equipment for personal or commercial purposes; the PURCHASER, having inspected the equipment or materials or having waived such inspection, understands and agrees that RTI does not guarantee or warranty the quality, performance or condition of the equipment, or its component parts, assemblies or accessories; nor does RTI guarantee or warranty the operational capability or functional performance for any length of time before or after the date of acceptance. The PURCHASER further agrees that RTI shall have no liability for any consequential commercial or personal damages, including liability for materials or labor, resulting from the sale of this merchandise. BSC-2 INSPECTION: BIDDERS ARE REQUIRED TO ATTEND A COMPULSORY SITE VISIT TO INSPECT THE OFFERED PROPERTY PRIOR TO SUBMITTING AN OFFER AND TO UNDERSTAND THE LOGISTICS OF THE REMOVAL OF ITEMS FROM THE RTI COMPOUND. All items included in the sale are located in the RTI Hilla Compound and may be seen only by appointment. Parties interested in bidding will be provided with a date and time of a site inspection of the equipment. Failure to make an inspection will not relieve the successful bidder (s) from their obligations to perform. BSC-3 PAYMENT: A 50% non-refundable down payment must be provided within 24 hours of the awarding of the RFQ. The full amount of the purchase price shall be due and payable in the form of cash on the day of the collection as well as signing the DD 1149 and Sold As Is forms prior to the collection. BSC-4 REMOVAL DATE: The equipment shall be removed by the successful bidder(s) on the date specified at the site inspection. The successful bidder(s) will be contractually obligated to remove from the premises all items in the lot(s) by this date. BSC-5 CONDITION: All items are offered on a "where-is-as-is basis with no warranties or representations, implied or express, offered to the purchaser. BSC-6 DISASSEMBLY/REMOVAL: Some items may require disassembly in order to be removed from the RTI Compound. Bidders should thoroughly inspect the equipment location to determine the need for disassembly. The successful bidder(s) must provide their own tools, equipment, and personnel for disassembly and removal. RTI personnel will not be available to disassemble, remove or load unless prior arrangements have been made with RTI. The costs for any such services rendered by RTI will be charged to the successful bidder.

BSC-7 BID ACCEPTANCE: Unless otherwise indicated by the bidder, it is understood and agreed that the bid will be valid for acceptance by RTI for a period of thirty (30) calendar days beyond the bid due date. BSC-8 ACCEPTANCE AND REJECTION: RTI reserves the right to reject any and all bids and to waive informalities in bidding. Bids may be rejected that are below what RTI considers to be a minimum acceptable price.

Indian Journal of Chemistry Vol. 48B, October 2009, pp. 1431-1434
Microwave assisted synthesis of some novel pyrimidinones/thiones
Satheesha Rai Na, Balakrishna Kallurayaa*, Lingappa Ba & Shalini Shenoyb
Keeping in view of these observations it was planned to synthesize a novel series of pyrimidinones/thiones in the one pot reaction of appropriate aldehydes, ethylacetoacteate and substituted urea/thiourea under microwave irradiation technique. Results and Discussion The reaction between substituted aldehyde 1, substituted urea 2 and ethylacetoacetate 3 in ethanol medium in the presence of an acid catalyst under microwave irradiation resulted in the formation of 1substituted-4-aryl-5-ethoxycarbonyl-6-methyl-pyrimidine-2-one/ thiones 4a-i (Scheme I). The generality of this method with respect to various precursors is summarized in Table I. The starting materials except phenyl thiourea obtained commercially and were used after purification. Phenylthiourea was prepared by refluxing aniline and ammonium thiocyanate in presence of hydrochloric acid. The structure of the newly synthesized compounds was established on the basis of analytical data IR, 1H NMR and mass spectra. Further in a representative example for compound 4c the structure was confirmed by recording its single crystal X-ray Figure 1. Biological activities The newly synthesized compounds 4a-i were screened for their antibacterial and antifungal activity. The bacteria employed were Staphylococcus aureus, Bacillus subtilis, Escherichia coli and Pseudomonas aeruginosa and the antifungal activity was tested against the fungus Candida albicans. The screening results indicated that among the compounds tested 4a-c showed significant activity against all the microorganisms tested and were active at a very low concentration compared to the standards employed Furacin and Flucanazole (Table II). Experimental Section General Melting points were determined by open capillary method and are uncorrected. All compounds were analyzed satisfactorily for C, H, and N. 1H NMR spectra were recorded on a Bruker AC 300F (400 MHz) NMR spectrometer using CDCl3 as
Department of Studies in Chemistry, Mangalore University, Mangalagangothri 574 199, India
Department of Microbiology, KMC, Mangalore, India E- mail: bkalluraya@gmail.com
Received 25 July 2007; accepted (revised) 5 June 2009 A novel series of 1-substituted-4-aryl-5-ethoxycarbonyl-6methylpyrimidine-2-ones/thiones are prepared in the one pot condensation of appropriate aldehyde, ethylacetoacetate and substituted urea in ethanol medium under microwave irradiation. The new compounds are well characterized by IR, 1H NMR, mass spectra, C,H,N-analysis and in a typical example the structure was further confirmed by X-ray crystallographic data. Keywords: Microwave biological activity synthesis, pyrimidinones, thiones,
Dihydropyrimidinones are an important class of compounds and gaining increasingly importance due to their therapeutic and pharmacological properties1. They have emerged as the integral backbones of several calcium channel blockers, anti-hypertensive agents and alpha-1-antagonists. Recently several isolated marine alkaloids with interesting biological activities were also found to contain the dihydropyrimidinone-5-carboxylate core. Most notable among them are the batzelladine alkaloids, which have been found to be potent human immunodeficiency virus (HIV) gp-120-CD4 inhibitors2. In modern laboratories organic transformations must be rapidly executed and products readily purified. Clearly there will be a continuing need for the definition of novel reaction routes to both multifunctional scaffolds for lead generation and to unique drug like heterocyclic structures. In this field controlled microwave irradiation has proved to be a powerful tool for both speeding up chemical optimizations and for efficient preparation of new target compounds3-6. The recent development in highly chemoselective metal catalyzed coupling reactions has further enabled direct incorporation of wide variety of chemical functionalities that previously were difficult to accomplish7,8.
INDIAN J. CHEM., SEC B, OCTOBER 2009

X H2 N NHR R2 R3

CHO R1

EtO 2C

R2 R3 H3C

R1 EtO 2C NH N R X

MW,EtOH
R=H/Ph X=O/S R1=H/NO2 R2=H/OMe R3=OMe/N,N(Et)2/SMe

Scheme I Table I Characterization data of pyrimidinones/thiones 4a-i Compd 4a R H X O R1 NO2 R2 OMe R3 OMe Mol.Fomula. M.W. Irrdn Time (Min) 3 3.2.4 3.5 3.Yield (%) 58 m.p. (C) 195-97 160-63 185-87 160-62 150-53 140-42 180-82 197-199 135-37 Nature of the solid Yellow Crystals Yellow Crystals Orange Crystals Yellow Crystals Yellow Crystals Yellow Crystals Orange Crystals Brown Powder Orange Crystals Found (Calcd)% C H N 52.50 (52.6 50.51 (50.39 57.78 (57.76 58.88 (58.82 55.84 (55.90 63.25 (63.31 65.20 (65.25 62.20 (62.24 68.00 (68.08 5.16 5.20 5.09 4.98 5.07 5.03 5.80 5.88 5.50 5.59 5.56 5.52 7.46 7.55 7.11 7.20 6.81 6.85 11.46 11.50) 10.91 11.02) 9.10 9.19) 9.11 9.15) 8.62 8.69) 7.14 7.03) 12.57 12.68) 12.21 12.10) 9.96 9.92)
C16H19N3OH S NO2 OMe OMe C16H19N3O6S 4b 381 Ph S NO2 OMe OMe C22H23N3O6S 4c 457 H O H H SMe C15H18N2O3S 4d 306 H S H H SMe C15H18N2O2S2 4e 322 Ph S H H SMe C21H22N2O2S2 4f 398 C18H25N3O3 H O H H N-(Et)2 4g 331 H S H H N-(Et)2 C18H25N3O2S 4h 347 Ph S H H N-(Et)2 C24H29N3O2S 4i 423 Solvent for recrystalization: Ethanol +DMF (2:1)
solvent and TMS as internal standard. Mass spectra were recorded either on a Jeol JMS-D 300 mass spectrometer or API 3000 LCMS instrument operating at 70 eV.
Procedure for the preparation of phenylthiourea Aniline (0.1 mole) was dissolved in minimum amount of dilute hydrochloric acid in a round bottomed flask. Ammonium thiocyanate (0.2 mole)
was then added and the mixture was refluxed for 5-6 hr. After cooling, the product separated was filtered and washed several times with cold water and recrystallized from ethanol. General procedure for the synthesis of 1-substituted-4-aryl-5-carboxyethyl-6-methyl-pyrimidine2-one/thiones 4a-i A mixture of substituted aldehyde (0.01 mole), ethylacetoacetate (0.015 mole), urea/thiourea/phenylthiourea (0.01mole) and Conc.H2SO4 (1-2 drops) in absolute ethanol (10mL) were taken in a borosil beaker (100 mL) was zapped9 inside the microwave oven for a period of 3-4 minutes (at 160 W i.e. 25% microwave power). The reaction- mixture was then allowed to stand at RT and the product formed was filtered, washed with ethanol, water, dried and recrystallized from ethanol to afford 4a-i in 52-68%
yield (microwave oven: LG-Little Chef MS-192W). The characterization data of the compounds 4a-i is given in Table I. Spectral data for compounds 4a-i 4a: Ethyl 4-(4,5-dimethoxy-2-nitrophenyl)-6-methyl2 oxo -1, 2, 3, 4-tetrahydropyrimidine-5-carboxylate 1 H NMR (400 MHz), Solvent CDCl3: 1.01 (t, 3H, CH3 of ethyl group), 2.49 (s, 3H, Me), 3.95 (s, 3H, OCH3) and 3.98 (s, 3H, OCH3), 4.04 (q, 2H, CH2 of ethyl group), 5.99 (s, 1H, CH), 6.78 (s, 1H, NH), 7.27 (s, 1H, Ar-H), 7.63 (s, 1H, ArH), 8.40 (s, 1H, NH);.MS: m/z 365 for C16H19N3O7. 4b: Ethyl 4-(4,5-dimethoxy-2-nitrophenyl)-6-methyl2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate 1 H NMR (400 MHz), CDCl3: 1.02 (t, 3H, CH3 of ethyl group), 2.50 (s, 3H, Me), 3.96 (s, 3H, OCH3) and 3.98 (s, 3H, OCH3), 4.02 (q, 2H, CH2 of ethyl group), 5.99 (s, 1H, CH), 6.78 (s, 1H, NH), 7.27 (s, 1H, Ar-H), 7.61(s, 1H, ArH), 8.09(s, 1H, NH); MS: m/z 381 for C16H19N3O6S. 4c: Ethyl-4-(4,5-dimethoxy-2-nitrophenyl)-6-methyl-1-phenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5carboxylate 1H NMR (400 MHz), CDCl3: 1.03 (t, 3H, CH3 of ethyl group), 2.28 (s, 3H, Me), 4.01(s, 6H, 2xOMe), 4.04 (q, 2H, CH2 of ethyl group), 6.05 (s, 1H, CH), 6.98(s, 1H, NH) 7.27 -7.61(m, 7H, ArH); MS: m/z 457 for C22H23N3O6S. 4d: Ethyl-4-[4-(methylthio)phenyl]-6-methyl-2-oxo1,2,3,4-tetrahydropyrimidine-5-carboxylate 1H NMR (400 MHz), CDCl3: 1.16 (t, 3H, CH3 of ethyl group), 2.35 (s, 3H, Me), 2.45 (s, 3H, SMe), 4.08 (q,

Figure 1 X-ray Crystallographic structure of compound 4c
Table II Antibacterial and antifungal activity data of compounds 4a-i Compd. Antibacterial activity (MIC in g/mL) S. aureus 4a 4b 4c 4d 4e 4f 4g 4h 4i Standard:Furacin Standard:flucanazol DMF 0.125 0.125 0.125 0.25 0.5 0.25 0.25 0.25 0.25 0.5 E. coli 0.125 0.125 0.125 0.25 0.25 0.25 0.25 0.25 0.25 0.5 P. aeruaginosa 0.125 0.125 0.125 0.25 0.25 0.25 0.25 0.25 0.25 0.25 B. subtilis 0.125 0.125 0.125 0.25 0.25 0.25 0.25 0.25 0.25 0.5 Antifungal activity (MIC in g/mL) C. albicans 0.125 0.125 0.125 0.25 0.25 0.25 0.25 0.25 0.25 0.25 -
2H, CH2 of ethyl group), 5.34 (s, 1H, CH), 7.16-7.27 (m, 4H, ArH), 7.94 (s, 1H, NH) 8.51(s, 1H, NH). 4e: Ethyl-4-[4-(methylthio)phenyl]- 6-methyl-2thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate 1H NMR (400 MHz), CDCl3: 1.18 (t, 3H, CH3 of ethyl group), 2.36 (s, 3H, Me), 2.46 (s, 3H, SMe), 4.09 (q, 2H, CH2 of ethyl group), 5.35 (s, 1H, CH), 7.16 -7.27 (m, 4H, ArH) 7.94 (s, 1H, NH) 8.51 (s, 1H, NH); MS:m/z 322 for C15H18N2O2S2. 4f: Ethyl-4-[4-(methylthio)-phenyl]-6-methyl -1phenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate 1H NMR (400 MHz), CDCl3: 1.22 (t, 3H, CH3 of ethyl group), 2.15 (s, 3H, Me), 2.53 (s, 3H, SMe), 4.14 (q, 2H, CH2 of ethyl group), 5.43 (s, 1H, CH), 7.23 -7.48 (m, 9H, ArH) 8.08 (s, 1H, NH); MS: m/z 398 for C21H22N2O2S2. 4h: Ethyl 4-[4-(dimethylamino) phenyl]-6-methyl2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate. MS: m/z 347 for C18H25N3O2S.
Acknowledgements The authors thank Head, RSIC, Chandigarh, for spectral and analytical data. The authors are also thankful to UGC, New Delhi for the financial assistance in the form of a Major Research Project. References
1 Beginelli P, Gazz Chim Ital, 23, 1893, 360. 2 Maryam M A, Mohammad B & Maryam H, Synth Commun, 34, , 2004, 3335. 3 Lidstrom P, Tierney J, Wathey B & Westman J, Tetrahedron, 57, 2001, 9225. 4 Larhed M & Hallberg A, Drug Discovery Today, 6, 2001, 406. 5 Kappe C O, Curr opin Chem Biol, 6, 2002, 314. 6 Kappe C O AngewChem Int Edn, 43, 2004, 6250. 7 Handbook of organopalladium Chemistry for Organic Synthesis, edited by E I Negishi, (Wiley Interscience, NewYork ), 2002, 1. 8 Singh K, Singh S & Mahajan A, J Org Chem, 70, 2005, 6114. 9 Bose A K, Manhas M S, Ghosh M, Raju V S, Taberi K & Urbanczyk L, Heterocycles, 30, 1990, 741.