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wuhuajiang

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[交流] [急]麻烦帮我查一个反应，用CA，BEILSTAIN

请大家帮忙查一反应
附件见http://free.ys168.com/?organic
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Potassium Alkenyl- and Aryltrifluoroborates: Stable and Efficient Agents for Rhodium-Catalyzed Addition to Aldehydes and Enones.     Batey, Robert A.; Thadani, Avinash N.; Smil, David V.    Department of Chemistry Lash Miller Chemical Laboratories,  University of Toronto,  Toronto,  ON,  Can.    Organic Letters  (1999),  1(10),  1683-1686.

t-Bu-Amphos-RhCl3.3H2O. A highly recyclable catalyst system for the cross-coupling of aldehydes and aryl- and alkenylboronic acids in aqueous solvents.     Huang, Rongcai; Shaughnessy, Kevin H.    Department of Chemistry and the Center for Green Manufacturing,  The University of Alabama,  Tuscaloosa,  AL,  USA.    Chemical Communications (Cambridge, United Kingdom)  (2005),   (35),  4484-4486.

[ Last edited by peak21st on 2006-6-21 at 17:18 ]
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4-oxo-4-p-tolylbutanoic acid
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Bibliographic Information

Highly chemoselective hydrogenation method using novel finely dispersed palladium catalyst on silk-fibroin: its preparation and activity.      Ikawa, Takashi; Sajiki, Hironao; Hirota, Kosaku.    Laboratory of Medicinal Chemistry,  Gifu Pharmaceutical University,  5-6-1 Mitahora-higashi, Gifu,  Japan.    Tetrahedron  (2005),  61(8),  2217-2231.  Publisher: Elsevier B.V.,  CODEN: TETRAB  ISSN: 0040-4020.  Journal  written in English.    CAN 142:355011    AN 2005:125076    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))   

Abstract

A palladium-fibroin complex (Pd/Fib) was prepd. by soaking silk-fibroin in MeOH soln. of Pd(OAc)2 for 2 days (under Ar atm.)-4 days (under air).  Pd(OAc)2 was gradually absorbed by fibroin and the rapid redn. of fibroin conjugated Pd(OAc)2 proceeded with MeOH as a reductant at room temp. to be the Pd(0) complex.  Pd/Fib catalyzed chemoselective hydrogenation of acetylenes, olefins and azides in the presence of arom. ketones and aldehydes, halides, N-Cbz protective groups and benzyl esters which are readily hydrogenated using Pd/C or Pd/C(en) as a catalyst.

Bibliographic Information

Synthesis of new 2-arylidene-4-(4-methylphenyl)but-3-en-4-olides and their pyrrolone derivatives.      Husain, Asif; Hasan, S. M.; Lal, Sukhbir; Alam, M. Mumtaz.    Department of Pharmaceutical Chemistry, Faculty of Pharmacy,  Jamia Hamdard (Hamdard University),  New Delhi,  India.    Indian Journal of Heterocyclic Chemistry  (2004),  14(2),  163-164.  Publisher: Prof. R. S. Varma,  CODEN: IJCHEI  ISSN: 0971-1627.  Journal  written in English.    CAN 142:447068    AN 2005:82984    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))   

Abstract

Starting from 3-(4-methylbenzoyl)propionic acid and using appropriate reagents some 2-arylidene-4-(4-methylphenyl)but-3-en-4-olides and corresponding pyrrolone derivs. were synthesized.

Bibliographic Information

Synthesis and anticonvulsant activity of 6-(substituted aryl)-2,3,4,5-tetrahydro-3-pyridazinones.      Siddiqui, Anees A.; Shahroz, Mir Mohammad; Amir, Mohammad.    Department of Pharmaceutical Chemistry, Faculty of Pharmacy,  Hamdard University,  New Delhi,  India.    Oriental Journal of Chemistry  (2004),  20(2),  303-306.  Publisher: Oriental Scientific Publishing Co.,  CODEN: OJCHEG  ISSN: 0970-020X.  Journal  written in English.    CAN 142:113996    AN 2004:988578    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))   

Abstract

6-(Substituted aryl)-2,3,4,5-tetrahydro-3-pyridazinones were obtained from hydrazinolysis of the appropriate -(substituted aroyl)propionic acid.  The title compds. showed promising anticonvulsant activity when evaluated by Electroconvulsometer.

Bibliographic Information

3-(4-bromobenzoyl)propanoic acid.      Seed, Alexander J.; Sonpatki, Vaishali; Herbert, Mark R.    USA.    Organic Syntheses  (2003),  Volume Date 2002,  79  204-208.  Publisher: John Wiley & Sons, Inc.,  CODEN: ORSYAT  ISSN: 0078-6209.  Journal  written in English.    CAN 141:23258    AN 2004:342265    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))   

Abstract

This method requires low reaction temps. and extended reaction times.  It provides consistently high yields and regioselective product formation and represents the first general method for the acylation of aryl compds. using succinic anhydride (dihydro-2,5-furandione).  The aluminum chloride-mediated Friedel-Crafts acylation of bromobenzene with dihydro-2,5-furandione gave 4-bromo--oxobenzenebutanoic acid.  A similar reaction of 2-bromothiophene with dihydro-2.5-furandione gave 5-bromo--oxo-2-thiophenebutanoic acid.

Bibliographic Information

Synthesis and antiinflammatory activity of 6-(substituted-aryl)-2,3,4,5-tetrahydro-3-thiopyridazinones.      Siddiqui, Anees A.; Kushnoor, Ashok; Wani, Sachin M.    Department of Pharmaceutical Chemistry, Faculty of Pharmacy,  Hamdard University,  New Delhi,  India.    Indian Journal of Heterocyclic Chemistry  (2004),  13(3),  257-260.  Publisher: Prof. R. S. Varma,  CODEN: IJCHEI  ISSN: 0971-1627.  Journal  written in English.    CAN 141:314269    AN 2004:298681    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))   

Abstract

Title 6-(substituted-aryl)-2,3,4,5-tetrahydro-3-thiopyridazinones were synthesized via Friedel-Crafts acylation of appropriate hydrocarbons with succinic anhydride in presence of anhyd. aluminum chloride followed by cyclization of -(substituted-aroyl)-propionic acid with hydrazine hydrate and sulfuration with phosphorus penta-sulfide.  All thiopyridazinones exhibited dose dependent varying degrees of antiinflammatory activity at a dose level of 15 mg/kg when evaluated by rat paw edema method.  The substituents in the Ph group at 6-position of the thiopyridazinone ring have been found to exert variable effect on the antiinflammatory activity.  Thus, benzoylpropionic acid (I) was prepd. in 73% by reaction of benzene with succinic anhydride.  Cyclization of I with hydrazine hydrate gave 6-phenyl-2,3,4,5-tetrahydro-3-pyridazinone (II) in 80% yield.  Sulfuration of II with phosphorus penta-sulfide gave title compd. 6-phenyl-2,3,4,5-tetrahydro-3-thiopyridazinone in 65% yield.

Bibliographic Information

An alternative route to syntheses of aryl keto acids in a chloroaluminate ionic liquid.      Mohile, Swapnil S.; Potdar, Mahesh K.; Salunkhe, Manikrao M.    Dep. Chem.,  The Inst. Sci.,  Mumbai,  India.    Journal of Chemical Research, Synopses  (2003),   (10),  650-651.  Publisher: Science Reviews,  CODEN: JRPSDC  ISSN: 0308-2342.  Journal  written in English.    CAN 140:339017    AN 2004:172175    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))   

Abstract

The Lewis acidic 1-butyl-3-methylimidazolium chloroaluminate ionic liq. [bmim]Cl.AlCl3, N=0.67, is employed as a catalyst as well as the solvent for the quick and efficient syntheses of aryl keto acids by Friedel-Crafts acylation and aroylation of arom. hydrocarbons using cyclic acid anhydrides.

Bibliographic Information

A simple procedure for the isolation of  -oxobenzenebutanoic acid derivatives: Application to the synthesis of fenbufen.      Srinivas, Ch.; Raju, C. M. Haricharan; Acharyulu, Palle V. R.    Technology Development Centre,  Custom Chemical Services Dr. Reddy's Laboratories,  Hyderabad,  India.    Organic Process Research & Development  (2004),  8(2),  291-292.  Publisher: American Chemical Society,  CODEN: OPRDFK  ISSN: 1083-6160.  Journal  written in English.    CAN 140:303369    AN 2004:129363    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))   

Abstract

A simple, convenient, and industrially viable process for the isolation of 4-oxobutanoic acid derivs., resulting from Friedel-Crafts acylation of arom. hydrocarbons with succinic anhydride, is reported.  The isolation procedure involved simple quenching of the reaction mixt. followed by filtration to give the product in good yield and with excellent purity.  The generality of the procedure has been demonstrated with representative examples of arom. hydrocarbon precursors and has also been applied to the isolation of fenbufen (I).  The quantity of aluminum chloride used in the reaction has also been optimized to reduce the load on effluent.  



Bibliographic Information

Calorimetric Approach and Simulation for Scale-Up of a Friedel-Crafts Reaction.      Gigante, Lucia; Lunghi, Angelo; Martinelli, Simone; Cardillo, Paolo; Picello, Luca; Bortolaso, Roberto; Galvagni, Marco; Rota, Renato.    Stazione Sperimentale per i Combustibili,  San Donato Milanese,  Italy.    Organic Process Research & Development  (2003),  7(6),  1079-1082.  Publisher: American Chemical Society,  CODEN: OPRDFK  ISSN: 1083-6160.  Journal  written in English.    CAN 140:61304    AN 2003:876856    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))   

Abstract

Exptl. calorimetric techniques and simulation techniques join together to optimize the scale-up of a Friedel-Crafts acylation.  The adopted methodol. involved the execution of isothermal tests at different temps., using the reaction calorimeter RC1, to obtain the heat flow vs. time data.  These data were used to perform a kinetic study of the reaction by using the simulation software BatchCAD.  The reliability of the adopted kinetic model was confirmed by comparing the exptl. data obtained by operating the desired reaction in adiabatic mode (in a Phi-Tec II calorimeter) with the predictions of the kinetic model in the same conditions.  Using this kinetic equation it was possible to simulate the process under pilot-plant conditions.  The good agreement between the model predictions and the exptl. data confirmed the accuracy of the kinetic equations.  Finally several large-scale prodn.-plant simulations were carried out varying both dosing time and reaction temp. to maximize the space/time yield and minimize the thermal risks.  This led to a high quality and safe process, saving a large part of the time (and money) usually spent in traditional scale-up procedures.

Bibliographic Information

An efficient and novel method for the synthesis of  -aroylpropionic acids under solvent-free conditions.      Mogilaiah, K.; Vasudeva Reddy, N.; Randheer Reddy, G.    Department of Chemistry,  Kakatiya University,  Warangal,  India.    Synthetic Communications  (2003),  33(18),  3109-3113.  Publisher: Marcel Dekker, Inc.,  CODEN: SYNCAV  ISSN: 0039-7911.  Journal  written in English.    CAN 140:93739    AN 2003:626348    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))   

Abstract

A simple and rapid reaction of succinic anhydride with arom. hydrocarbons is described.  The reaction is conducted under Friedel-Crafts conditions in the absence of solvent at room temp. using aluminum chloride as catalyst.

[ Last edited by peak21st on 2006-6-22 at 12:11 ]
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Synthesis and anti-inflammatory activity of 1,4-dihydropyridines.      Bahekar, Sushilkumar; Shinde, Devanand.    Department of Chemical Technology,  Dr. Babasaheb Ambedkar Marathwada University,  Aurangabad,  India.    Acta Pharmaceutica (Zagreb, Croatia)  (2002),  52(4),  281-287.  Publisher: Croatian Pharmaceutical Society,  CODEN: ACPHEE  ISSN: 1330-0075.  Journal  written in English.    CAN 139:69125    AN 2003:147387    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))  

Abstract

1,4-Dihydropyridines have been synthesized by treating different arom. aldehydes with b-aroylpropanoic acid and ammonia.  The structures of the new compds. were established on the basis of 1H NMR and IR spectral data.  Anti-inflammatory activity in vivo was evaluated and compared with the std. drug, diclofenac sodium.  Some compds. showed moderate activity.

Bibliographic Information

Studies on butenolides: 2-arylidene-4-(substituted aryl)but-3-en-4-olides-synthesis, reactions and biological activity.      Khan, M. S. Y.; Husain, A.; Sharma, S.    Department of Pharmaceutical Chemistry, Faculty of Pharmacy,  Jamia Hamdard (Hamdard University),  New Delhi,  India.    Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry  (2002),  41B(10),  2160-2171.  Publisher: National Institute of Science Communication,  CODEN: IJSBDB  ISSN: 0376-4699.  Journal  written in English.    CAN 138:304101    AN 2002:903527    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))  

Abstract

2-Arylidene-4-(substituted aryl)but-3-en-4-olides also known as 3-arylidene-5-(substituted aryl)-2(3H)-furanones have been prepd. from 3-(substituted aroyl) propionic acid and arom. aldehydes.  Some of the selected butenolides have been reacted with ammonia and benzylamine to give corresponding pyrrolones and N-benzylpyrrolones resp. and characterized on the basis of 1H NMR and Mass spectrometric data and elemental anal. results.  These compds. have been tested for anti-inflammatory and antimicrobial actions.

Bibliographic Information

A practical procedure for the synthesis of esonarimod, (R,S)-2-acetylthiomethyl-4-(4-methylphenyl)-4-oxobutanoic acid, an antirheumatic agent (part 1).      Noguchi, Toshiya; Onodera, Akira; Tomisawa, Kazuyuki; Yokomori, Sadakazu.    Medicinal Research Laboratories,  Taisho Pharmaceutical Co., Ltd.,  Saitama,  Japan.    Chemical & Pharmaceutical Bulletin  (2002),  50(10),  1407-1412.  Publisher: Pharmaceutical Society of Japan,  CODEN: CPBTAL  ISSN: 0009-2363.  Journal  written in English.    CAN 138:254903    AN 2002:858564    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))  

Abstract

An efficient and practical procedure for the synthesis of esonarimod, (R,S)-2-acetylthiomethyl-4-(4-methylphenyl)-4-oxobutanoic acid (I), a new antirheumatic drug, has been developed.  The intermediate, 2-methylene-4-(4-methylphenyl)-4-oxobutanoic acid (II), was prepd. by Friedel-Crafts acylation of toluene with itaconic anhydride in the presence of aluminum trichloride and nitrobenzene in 63% yield without silica gel column purifn.  Compd. I was prepd. by Michael addn. of II with thioacetic acid in 74% yield.  Overall, I was obtained in 47% yield from itaconic anhydride.  The structures and synthetic mechanisms of byproducts (five compds.) of II were also clarified.

Bibliographic Information

Synthesis of some new prodrugs of sulphonamides and studies on their antimicrobial and anti-inflammatory action.      Khan, M. S. Y.; Husain, A.; Hasan, S. M.; Akhter, M.    Department of Pharmaceutical Chemistry, Faculty of Pharmacy,  Jamia Hamdard (Hamdard University),  New Delhi,  India.    Scientia Pharmaceutica  (2002),  70(3),  277-286.  Publisher: Oesterreichische Apotheker-Verlagsgesellschaft,  CODEN: SCPHA4  ISSN: 0036-8709.  Journal  written in English.    CAN 138:337794    AN 2002:821007    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))  

Abstract

Various amide-based prodrugs of sulfonamides have been synthesized by condensing appropriate sulfonamide moiety with different b-aroyl propionic acids.  All the compds. have been evaluated for their antimicrobial and anti-inflammatory activities.  Their structures were established on the basis of elemental anal., 1H NMR and Mass spectral data.  Some of these compds. were found to have significant activity.

Bibliographic Information

Direct synthesis of g -butyrolactones via g -phenyl substituted butyric acids mediated benzyl radical cyclization.      Mahmoodi, N. O.; Jazayri, M.    Organic Research Laboratory, Department of Chemistry,  University of Guilan,  Rasht,  Iran.    Synthetic Communications  (2001),  31(10),  1467-1475.  Publisher: Marcel Dekker, Inc.,  CODEN: SYNCAV  ISSN: 0039-7911.  Journal  written in English.    CAN 135:272808    AN 2001:544574    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))  

Abstract

Synthesis of several g-butyrolactones with arom. substitution at carbon 5 from comparative g-aryl acids with 25-85% yield are covered.  The target compds. thus prepd. included, dihydro-5-phenyl-2(3H)-furanone, dihydro-5-(4-methylphenyl)-2(3H)furanone, dihydro-5-(4-methoxyphenyl)-2(3H)furanone, and 5-(1,1'-biphenyl-4-yl)dihydro-2(3H)-furanone.  The straight oxidn. in the presence of peroxydisulfate-copper(II)chloride system in aq. medium was applied.  The reaction is highly regioselective and leads exclusively to g-butyrolactone, through stable benzylic radical intermediate.

Bibliographic Information

Syntheses and antiinflammatory activity of some 6-aryl -2,3,4,5-tetrahydro-3-pyridazinones.      Khan, M. S. Y.; Siddiqui, Anees A.    Department of Pharmaceutical Chemistry,  Hamdard University,  New Delhi,  India.    Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry  (2000),  39B(8),  614-619.  Publisher: National Institute of Science Communication, CSIR,  CODEN: IJSBDB  ISSN: 0376-4699.  Journal  written in English.    CAN 134:100819    AN 2000:780158    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))  

Abstract

6-Aryl-2, 3, 4, 5-tetrahydro-3-pyridazinones I [R = Ph, 2-naphthyl, 4-MeOC6H4, 4-MeC6H4, 4-EtC6H4, 4-PhC6H4, 3,4-(MeO2)C6H3, Me2C6H3, 4-ClC6H4, 2-MeO-4-MeC6H3, 4-EtOC6H4, 4-(PhCH2)C6H3, 4-PhOC6H4, 3,4-Cl2C6H4, 2-thienyl; R1 = H, Ph] were prepd. by dehydrocyclization of hydrazides formed by reaction of RCOCH2CH2CO2Me with R1NHNH2 in the presence of anhyd. NaOAc.  I show promising antiinflammatory activity through evaluation by carrageenin induced paw edema test in rats.  


Bibliographic Information

Studies on antirheumatic agents:  3-benzoylpropionic acid derivatives.      Kameo, Kazuya; Ogawa, Kunio; Takeshita, Kimiyo; Nakaike, Shiro; Tomisawa, Kazuyuki; Sota, Kaoru.    Res. Cent.,  Taisho Pharm. Co., Ltd.,  Saitama,  Japan.    Chemical & Pharmaceutical Bulletin  (1988),  36(6),  2050-60.  CODEN: CPBTAL  ISSN: 0009-2363.  Journal  written in English.    CAN 110:57257    AN 1989:57257    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))  

Abstract

As part of the search for new antirheumatic agents, three types of 3-benzoylpropionic acid derivs., e.g. RCOCH2CH(SR1)CO2R2, RCOCH2CH(CH2SR1)CO2R2, and RCOCH(CH2SR1)CH2CO2R2 (R = Ph, substituted phenyl; R1 = Ac, Et, EtCO, Bz; R2 = H, Et, Me, CH2Ph), having a mercapto moiety in their structures were prepd. and tested for suppressing activity on adjuvant arthritis in Sprague-Dawley rats.  A structure-activity relationship study showed that substitution on the Ph ring contributed to the activity and the most favorable substituent was different in each type of deriv.

Bibliographic Information

Study of the alkylation of 6-oxo-1,6-dihydropyridazines by triethyloxonium tetrafluoroborate.      Volynets, N. F.; Samartseva, I. V.; Khramova, I. V.; Pavlova, L. A.    Leningr. Tekhnol. Inst.,  Leningrad,  USSR.    Zhurnal Organicheskoi Khimii  (1984),  20(8),  1760-4.  CODEN: ZORKAE  ISSN: 0514-7492.  Journal  written in Russian.    CAN 102:24570    AN 1985:24570    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))  

Abstract

Cyclization of RCOCH2CH2CO2H (R = Ph, p-Me-, -ClC6H4) with NH2NHR1 (R1 = Me, Ph) gave tetrahydropyridazinones I which on heating with Br in AcOH gave 63-81% dihydropyridazinones II.  Alkylation of II with Et3O×BF4 gave onium compds. III (X = BF4-) and is not dependent on the character of R and R1.  Treating III (X = BF4-) with HX (X = FeCl4, ClO4) gave III (X = FeCl4, ClO4).  


Bibliographic Information

Reactions with monohydrazones of dicarbonyl compounds, VI.  Syntheses of 4-oxocarboxylic acids and their esters by means of a -hydrazonoaldehydes.      Severin, Theodor; Poehlmann, Hans.    Inst. Pharm. Lebensmittelchem.,  Univ. Muenchen,  Munich,  Fed. Rep. Ger.    Chemische Berichte  (1978),  111(4),  1564-77.  CODEN: CHBEAM  ISSN: 0009-2940.  Journal  written in German.    CAN 89:23693    AN 1978:423693    CAPLUS   (Copyright (C) 2006 ACS on SciFinder (R))  

Abstract

a-Hydrazono aldehydes R1R2NN:CRCHO [I; R = Me, Pr, iso-Bu, Ph; R1 = H, Me; R2 = Ph, 4-O2NC6H4, 2,4-(O2N)2C6H3] were prepd. by oxidn. of R1R2NN:CRMe with SeO2 or by coupling of enamines RCH:CHNR3R4 (R3R4N = piperidino) with a benzenediazonium salt.  Treatment of I with Ph3P:CHCO2Et, AcOPh, or PhCH2CO2Et in the presence of base gave the 4-oxocarboxylate hydrazones R1R2NN:CRCH:CR5CO2Et (R5 = H, Ph), which underwent hydrolytic cleavage or reductive hydrolysis to RCOCH:CR5CO2Et or RCOCH2CHR5CO2Et.
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捐助贵宾 (著名写手)

单身家族之lucky
谢谢
呵呵
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9楼2006-06-23 00:36:36
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weixiaobao-000

至尊木虫 (著名写手)

探险者

SOS!!

那位大哥有下面这种物质的合成方法啊?帮忙用ＣＡ查一下吧！
我用CHEMDRAW命名的：penta-1,4-dien-3-one
我也不知道它的俗名是啥,最好能提供几篇相关文献吧!
请赐教啊!!
多谢了!
详细请见http://muchong.com/bbs/viewthread.php?tid=292786&fpage=1
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真爱如同关节炎，只有在你初次尝到它的滋味时，你才会相信它的存在！
10楼2006-08-15 16:54:37
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