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共查询到20条相似文献，搜索用时 15 毫秒

1.

Synthesis of 5-(hetarylmethylidene)pyrimidine-2,4,6(1<Emphasis Type=Italic>H</Emphasis>,3<Emphasis Type=Italic>H</Emphasis>,5<Emphasis Type=Italic>H</Emphasis>)-triones

E. A. Yurtaeva A. G. Tyrkov 《Russian Journal of Organic Chemistry》2016,52(2):289-291

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2.

Synthesis of 1,3-dihydro-2<Emphasis Type=Italic>H</Emphasis>-benzimidazol-2-ones (microreview)

Ramón Armenta Juan I. Sarmiento-Sánchez 《Chemistry of Heterocyclic Compounds》2016,52(12):1002-1004

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3.

Synthesis and halocyclization of 4-methylquinolin-2(1<Emphasis Type=Italic>H</Emphasis>)-one <Emphasis Type=Italic>N</Emphasis>- and <Emphasis Type=Italic>O</Emphasis>-methallyl derivatives

Dmitry G. Kim Evgeniya A. Vershinina Irina G. Ovchinnikova Pavel A. Slepukhin Marina A. Ezhikova Mikhail I. Kodess 《Chemistry of Heterocyclic Compounds》2018,54(10):977-980

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4.

Reaction of 5-arylfuran-2(3<Emphasis Type=Italic>H</Emphasis>)-ones with 3-formylchromone

T. V. Anis’kova E. G. Stulova A. Yu. Egorova 《Russian Journal of Organic Chemistry》2016,52(8):1215-1216

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5.

Polyfunctional pyrazoles 11*. Synthesis of 5-aroylpyrano[3,4-<Emphasis Type=Italic>c</Emphasis>]pyrazol-7(2<Emphasis Type=Italic>H</Emphasis>)-ones

Mykhailo K. Bratenko Marianna M. Barus Mykhailo V. Vovk 《Chemistry of Heterocyclic Compounds》2017,53(8):905-908

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6.

Reactivity of 8-substituted 7-amino-3-<Emphasis Type=Italic>tert</Emphasis>-butylpyrazolo[5,1-<Emphasis Type=Italic>c</Emphasis>][1,2,4]triazin-4(6<Emphasis Type=Italic>H</Emphasis>)-ones

L. M. Mironovich A. Yu. Podol’nikova 《Russian Journal of Organic Chemistry》2016,52(3):453-455

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7.

Alkylation of [1,2,4]triazolo[1,5-<Emphasis Type=Italic>a</Emphasis>][1,3,5]triazin-7(3<Emphasis Type=Italic>H</Emphasis>)-ones

Irina V. Ul′yankina Anna V. Zavodskaya Victor E. Parfenov Alexander A. Gidaspov Andrey K. Shiryaev Eugenia V. Selezneva Vladimir V. Bakharev 《Chemistry of Heterocyclic Compounds》2016,52(12):1054-1060

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8.

Synthesis and Characterization of <Emphasis Type=Italic>N</Emphasis><Superscript><Emphasis Type=Italic>3</Emphasis></Superscript>-(2,2,2-Trinitroethyl)-1,2,4-Oxadiazole-3,5-Diamine

David E. Chavez Maxwell C. Schulze Damon A. Parrish 《Chemistry of Heterocyclic Compounds》2017,53(6-7):737-739

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9.

Unexpected transformations of 11-acetyl-8-bromo-2-methyl-5,6-dihydro-2<Emphasis Type=Italic>H</Emphasis>-2,6-methano-1,3,5-benzoxadiazocin-4(3<Emphasis Type=Italic>H</Emphasis>)-one(thione)

Valentina F. Sedova Viktor P. Krivopalov Oleg P. Shkurko 《Chemistry of Heterocyclic Compounds》2017,53(10):1163-1166

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10.

Synthesis of 4,5-dihydro-1,4-benzothiazepin-3(2<Emphasis Type=Italic>H</Emphasis>)-one (microreview)

Taras M. Tarasiuk Olena O. Shyshkina 《Chemistry of Heterocyclic Compounds》2016,52(12):999-1001

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11.

Alkylation reactions of 5-amino-substituted tetrazolo[1,5-<Emphasis Type=Italic>a</Emphasis>][1,3,5]triazin-7(3<Emphasis Type=Italic>H</Emphasis>)-ones with alkyl halides

Victor E. Parfenov Vladimir V. Bakharev Alexander A. Gidaspov Andrey K. Shiryaev Pavel A. Slepukhin 《Chemistry of Heterocyclic Compounds》2016,52(12):1061-1069

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12.

Synthesis of benzo[<Emphasis Type=Italic>f</Emphasis>]coumarins from 2-trifluoroacetyl-1<Emphasis Type=Italic>H</Emphasis>-benzo[<Emphasis Type=Italic>f</Emphasis>]chromenes and 2-naphthols

Vitaly A. Osyanin Dmitry V. Osipov Yulia V. Popova Irina A. Semenova Yuri N. Klimochkin 《Chemistry of Heterocyclic Compounds》2016,52(12):1012-1016

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13.

Synthesis and Analgesic Activity of bis(3,4-dihydroquinoxalin-2(1<Emphasis Type=Italic>H</Emphasis>)-one) and bis(3,4-dihydro-2<Emphasis Type=Italic>H</Emphasis>-1,4-benzoxazin-2-one) Derivatives

Ivan V. Kulakov Anastasiya A. Karbainova Zarina T. Shulgau Tulegen M. Seilkhanov Yurii V. Gatilov Alexander S. Fisyuk 《Chemistry of Heterocyclic Compounds》2017,53(10):1094-1097

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14.

Synthesis and properties of 3-azido-4-(2<Emphasis Type=Italic>H</Emphasis>-tetrazol-5-yl)furazan

Andrei I. Stepanov Vladimir S. Sannikov Dmitry V. Dashko Aleksey G. Roslyakov Alexander A. Astrat’yev Elena V. Stepanova Zainutdin G. Aliev Tel’man K. Goncharov Sergei M. Aldoshin 《Chemistry of Heterocyclic Compounds》2017,53(6-7):779-785

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15.

2,3-Dihydro-1<Emphasis Type=Italic>H</Emphasis>-pyrrolo[1,2-<Emphasis Type=Italic>a</Emphasis>]indoles (microreview)

Anastasiya T. Plieva 《Chemistry of Heterocyclic Compounds》2017,53(2):153-155

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16.

Fischer indole synthesis of 3-benzyl-1<Emphasis Type=Italic>H</Emphasis>-indole <Emphasis Type=Italic>via</Emphasis> conductive and dielectric heating

Jesco Panther Julian Rechmann Thomas J. J. Müller 《Chemistry of Heterocyclic Compounds》2016,52(11):897-903

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17.

Catalyst-free green synthesis of novel 2-amino-4-aryl-3-(4-fluorophenyl)-4,6,7,8-tetrahydroquinolin-5(1<Emphasis Type=Italic>H</Emphasis>)-ones <Emphasis Type=Italic>via</Emphasis> a one-pot four-component reaction under ultrasonic condition

Santhosh Govindaraju Sumaiya Tabassum Riyaz-ur-Rahaman Khan Mohamed Afzal Pasha 《Chemistry of Heterocyclic Compounds》2016,52(11):964-969

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18.

Synthesis of diheteroaryl sulfides <Emphasis Type=Italic>via</Emphasis> chemoselective reaction of 4,6-diaminopyrimidine-2(1<Emphasis Type=Italic>H</Emphasis>)-thione with haloheteroaryl compounds

Tayebeh Davodian Reza Ranjbar-Karimi Hossein Mehrabi 《Chemistry of Heterocyclic Compounds》2017,53(10):1120-1123

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19.

Synthesis and properties of symmetrical <Emphasis Type=Italic>N</Emphasis>,<Emphasis Type=Italic>N</Emphasis>'-Bis(R-adamantan-1-yl)ureas as target-oriented soluble epoxide hydrolase (sEH) inhibitors

G. M. Butov V. V. Burmistrov V. S. D’yachenko 《Russian Journal of Organic Chemistry》2017,53(7):977-980

Self-condensation of substituted adamantan-1-yl isocyanates in THF in the presence of DBU afforded 91–96% of symmetrical ureas as target-oriented soluble epoxide hydrolase (sEH) inhibitors. The described reaction avoids the use of the corresponding amine as counterpart. The obtained ureas are characterized by reduced melting points and improved solubility in water. 相似文献

20.

Physicochemical properties and antimicrobial activity of new spirocyclic thieno[2,3-<Emphasis Type=Italic>d</Emphasis>]pyrimidin-4(3<Emphasis Type=Italic>H</Emphasis>)-one derivatives

Modesto de Candia Claudia Altamura Nunzio Denora Saverio Cellamare Manuel Nuzzolese Danila De Vito Leonid G. Voskressensky Alexey V. Varlamov Cosimo D. Altomare 《Chemistry of Heterocyclic Compounds》2017,53(3):357-363

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