共查询到20条相似文献,搜索用时 62 毫秒
1.
Moslem Mansour Lakouraj Masoud Mokhtary 《Monatshefte für Chemie / Chemical Monthly》2009,140(1):53-56
Abstract A Mild and efficient method for preparing amides by reaction of nitriles with benzhydrol and tertiary alcohols is described
using polyvinylpolypyrrolidone-supported boron trifluoride. Selective amidation of benzhydrol in the presence of primary benzyl
alcohols was also achieved.
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2.
Farhad Shirini Mohammad Ali Zolfigol Masoumeh Abedini 《Monatshefte für Chemie / Chemical Monthly》2009,140(1):61-64
Abstract Saccharin sulfonic acid was easily prepared by the reaction of saccharin with neat chlorosulfonic acid at room temperature.
This reagent is efficiently able to catalyze the chemoselective trimethylsilylation of alcohols with hexamethyldisilazane
in the presence of amines and thiols.
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3.
Min Wang Zhi-Guo Song Hong Gong Heng Jiang 《Monatshefte für Chemie / Chemical Monthly》2009,140(2):177-179
Abstract Tetrahydropyranylation of alcohols and phenols was accomplished successfully using copper nitrate and acetic acid as a synergistic
catalyst at room temperature under solvent-free condition. Compared with other synergistic catalytic systems, copper nitrate/acetic
acid proved to be the most efficient. Both alcohols (primary, secondary, tertiary, benzylic, cyclic, allyl, cinnamyl, and
furyl) and phenols reacted smoothly in high yields.
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4.
Marco Rupprich Clemens Decristoforo Barbara Matuszczak 《Monatshefte für Chemie / Chemical Monthly》2009,140(4):405-407
Abstract In contrast to the results presented in a previous report, the direct conversion of alcohols to alkyl fluorides with triphenylphosphine
and potassium fluoride in CCl4/DMF under mild conditions failed.
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5.
Abstract One-pot, three-components synthesis of 2,4,6-triarylpyridines and 5-unsubstituted-3,4-dihydropyrimidin-2(1H)-ones was performed under solvent-free conditions using molecular iodine as the catalyst in moderate to good product yields.
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6.
Kamal Amani Mohammad Ali Zolfigol Arash Ghorbani-Choghamarani Maryam Hajjami 《Monatshefte für Chemie / Chemical Monthly》2009,140(1):65-68
Abstract A mild, efficient, and highly selective oxidation method of sulfides to sulfoxides using Fe(NO3)3·9H2O and catalytic amounts of KBr or NaBr in the presence of wet SiO2 (50% w/w) has been developed. A variety of aliphatic and aromatic sulfides were selectively oxidized at room temperature in good to
excellent yields.
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7.
Robabeh Baharfar Seyed M. Vahdat Fatemeh G. Hakimabadi 《Monatshefte für Chemie / Chemical Monthly》2009,140(5):489-493
Abstract An efficient one-pot reaction of dialkyl acetylenedicarboxylates with 2,4-dihydroxybenzo(or aceto)phenones in the presence
of triphenylphosphine produces 5-hydroxy- and 7-hydroxycoumarin derivatives. The novel procedure features short reaction time,
fairly good yields, and simple workup.
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8.
Mohammad Anary-Abbasinejad Hossein Anaraki-Ardakani Fatemeh Ghanea 《Monatshefte für Chemie / Chemical Monthly》2009,140(4):397-400
Abstract The reactive intermediate generated by the reaction of alkyl isocyanides and dialkyl acetylenedicarboxylates was trapped by
ethyl carbazones to produce stable ketenimine derivatives in good yield. The reaction is characterized by mild conditions,
high selectivity, and tolerance to various functional groups.
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9.
Ch. Sree Lakshmi H. Rehaman Adari Bhaskar Rao 《Monatshefte für Chemie / Chemical Monthly》2009,140(6):611-613
Abstract The enzymatic cyclization of phenoxyacetylcyanomethylenetriphenylphosphorane derivatives using pre-treated baker’s yeast cells,
a rapid one-pot assembly of heteromacrocyclic compounds, is described.
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10.
Issa Yavari S. Zahra Sayyed-Alangi Rahimeh Hajinasiri Hadi Sajjadi-Ghotbabadi 《Monatshefte für Chemie / Chemical Monthly》2009,140(2):209-211
Abstract A simple one-pot synthesis of functionalized ethyl 1,3-thiazole-5-carboxylates from the reaction of 2-chloro-1,3-dicarbonyl
compounds with thioureas or thioamides in the presence of 1-butyl-3-methylimidazolium trifluoromethanesulfonate is described.
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11.
Do-Min Lee Gullapalli Kumaraswamy Kee-In Lee 《Monatshefte für Chemie / Chemical Monthly》2009,140(1):73-78
Abstract Catalytic transfer hydrogenation of α-tosyloxyarylketones mediated by a chiral rhodium complex using an azeotropic mixture
of formic acid/triethylamine afforded the corresponding 1-arylethanediol monotosylates in excellent yield with high enantioselectivity.
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12.
Barahman Movassagh Mohammad Soleiman-Beigi 《Monatshefte für Chemie / Chemical Monthly》2009,140(4):409-411
Abstract A simple, highly efficient, and green protocol has been developed for preparation of sulfides from alkyl or aryl thiols and
benzyl-, allyl-, t-butyl, and adamantyl halides under solvent- and catalyst-free conditions.
Graphical abstract
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13.
Issa Yavari Rahimeh Hajinasiri S. Zahra Sayyed-Alangi 《Monatshefte für Chemie / Chemical Monthly》2009,140(2):205-207
Abstract 1-Ethyl-3-methylimidazolium bromide was used as a green recyclable alternative to volatile organic solvents for KOH catalyzed
three-component synthesis of diethyl alkylsulfanylmethylmalonates from aldehydes, diethyl malonate, and alkylthiols.
Graphical Abstract A synthesis of diethyl alkylsulfanylmethylmalonates catalyzed by KOH in an ionic liquid
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14.
Nagnnath D. Kokare Devanand B. Shinde 《Monatshefte für Chemie / Chemical Monthly》2009,140(2):185-188
Abstract Aromatic aldoximes were converted to the corresponding nitriles in good to excellent yields by employing phosphoric acid diethyl
ester 2-phenylbenzimidazol-1-yl ester as reagent. The method was equally effective for oximes bearing electron-donating and
electron-withdrawing substituents.
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15.
Adel A.-H. Abdel-Rahman Ahmed E.-S. Abdel-Megied Hamed M. Abdel-Bary Abdel-Aleem H. Abdel-Aleem Emad M. I. Morcy Mohamed T. Shabaan 《Monatshefte für Chemie / Chemical Monthly》2009,140(5):559-564
Abstract A series of peptide derivatives conjugated with N1-protected tryptophan residue was synthesized. The prepared compounds were tested for antimicrobial activity against four
different bacterial species displaying different degrees of antibacterial activities or inhibitory actions.
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16.
Jolanta Pawłowska Krzysztof K. Krawczyk Krystyna Wojtasiewicz Jan K. Maurin Zbigniew Czarnocki 《Monatshefte für Chemie / Chemical Monthly》2009,140(1):83-86
Abstract (+)-Lortalamine was synthesised using (S)-(−)-α-methylbenzylamine as a chiral auxiliary. The stereochemistry of an intermediate compound was established on the basis
of X-ray crystallography, allowing unambiguous assignment of the absolute configuration.
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17.
Abstract An efficient one-pot synthesis of amidoalkyl naphthols is described. This involves the three-component reaction of 2-naphthol,
aromatic aldehydes and amide or urea in the presence of a catalytic amount of 2,4,6-trichloro-1,3,5-triazine (TCT, cyanuric
chloride) under solvent-free conditions.
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18.
Emanuel Makrlík Jiří Dybal Petr Vaňura 《Monatshefte für Chemie / Chemical Monthly》2009,140(3):251-254
Abstract From extraction experiments in the two-phase water–nitrobenzene system and γ-activity measurements, the stability constant
of the valinomycin–lithium complex in nitrobenzene saturated with water was determined. Further, the structure of the resulting
complex was indicated by means of the density functional level of theory (DFT) calculations.
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19.
Abstract A polymer-supported Lewis acid catalyst was prepared and found to be extremely efficient for the preparation of imidazole
derivatives via three-component condensation of benzil, aldehydes, and ammonium acetate under mild conditions. The catalyst
is stable and can be easily recovered and reused at least four times without any loss of activity.
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20.
Mohammad A. Khalilzadeh Issa Yavari Zinatossadat Hossaini Hasan Sadeghifar 《Monatshefte für Chemie / Chemical Monthly》2009,140(4):467-471
Abstract A novel method for oxazine ring formation is established using the reaction of ammonium thiocyanate and acid chlorides with
napthols in the presence of N-methylimidazole to afford [1,3]oxazine-4-thione derivatives in excellent yields.
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