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Journal articles on the topic 'Phenylcarbamates'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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1

Rosevear, J., and JFK Wilshire. "A Comparison of the Reactions of Some Ethyl N-Arylcarbamates With Those of the Corresponding Acetanilides. II. Amidomethylation With N-Hydroxy-methylphthalimide." Australian Journal of Chemistry 43, no. 2 (1990): 339. http://dx.doi.org/10.1071/ch9900339.

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The reactions of some ethyl N- arylcarbamates and of the corresponding acetanilides towards 1 equiv. of N-hydroxymethylphthalimide in concentrated sulfuric acid at 50° have been compared with one another. In the case of certain para-substituted compounds, amidomethylation occurs more readily ortho to the carbamate group than to the N-acetyl group. The diagnostic use of (D6)benzene as a 1H n.m.r. solvent, particularly for the structural elucidation of the ortho-( phthalimidomethyl )- phenylcarbamates and -acetanilides, is reported. Acidic treatment of the ortho -( phthalimidomethyl ) phenylcarb

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2

Mona, Sobhi, Patrick Ravanel, Xavier de Chérade, Michel Bergon, Jean-Pierre Calmon, and Michel Tissut. "Uncoupling activity of some N-phenylcarbamates." Pesticide Biochemistry and Physiology 27, no. 3 (1987): 261–66. http://dx.doi.org/10.1016/0048-3575(87)90055-1.

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3

Daub, Jörg, Lothar Jakob, Josef Salbeck, and Yoshio Okamoto. "Modellverbindungen für Elektronentransfer in räumlich geordneten Systemen: Chirale und achirale Triptycenazulenchinone." CHIMIA 39, no. 12 (1985): 393. https://doi.org/10.2533/chimia.1985.393.

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Stable bitriptyceneazulene quinones have been prepared by Lewis acid induced coupling of triptyceneazulene quinones. Resolution of the enantiomers succeeded by high performance liquid chromatography (HPLC) on phenylcarbamates of cellulose. Some chiroptical properties of the enantiomers are reported. Electron transfer properties have been investigated by cyclovoltammetry.

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4

Hollomon, Derek W., Jenny A. Butters, Helen Barker та Len Hall. "Fungal β-Tubulin, Expressed as a Fusion Protein, Binds Benzimidazole and Phenylcarbamate Fungicides". Antimicrobial Agents and Chemotherapy 42, № 9 (1998): 2171–73. http://dx.doi.org/10.1128/aac.42.9.2171.

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ABSTRACT Benzimidazoles are important antitubulin agents used in veterinary medicine and plant disease control. Resistance is a practical problem correlated with single amino acid changes in β-tubulin and is often linked to greater sensitivity to phenylcarbamates. This negative cross-resistance creates opportunities for durable antiresistance strategies. Attempts to understand the molecular basis of benzimidazole resistance have been hampered by the inability to purify tubulin from filamentous fungi. We have overcome some of these problems by expressing β-tubulin as a fusion with a maltose bin

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5

Hajinasiri, Rahimeh, and Halimeh Khatoon Khajavi. "Reaction of N-Methylimidazole and Dimethyl Acetylenedicarboxylate in the Presence of N-Phenyl Carbamate under Solvent-free Conditions." Zeitschrift für Naturforschung B 69, no. 4 (2014): 439–43. http://dx.doi.org/10.5560/znb.2014-3318.

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An efficient synthesis of 1,2,3-functionalized imidazoles and dimethyl-2-[(alkoxycarbonyl)- anilino]-2-butenedioate derivatives via one-pot reactions between N-methylimidazole, dimethyl acetylenedicarboxylate and N-phenylcarbamates under solvent-free conditions is described. The mild reaction conditions and good yields exhibit the synthetic advantage of this method.

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6

Takahashi, Junya, Osamu Kirino, Chiyozo Takayama, and Katsuzo Kamoshita. "Studies on fungicidal activity of N-phenylcarbamates." Journal of Chromatography A 436 (January 1988): 316–22. http://dx.doi.org/10.1016/s0021-9673(00)94589-8.

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7

Haufe, Günter, Dörthe Wölker, and Roland Fröhlich. "Selectivity of Biohydroxylation withBeauveriabassianaoftrans-2-FluorocycloalkylN-Phenylcarbamates." Journal of Organic Chemistry 67, no. 9 (2002): 3022–28. http://dx.doi.org/10.1021/jo016332j.

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8

VELIKORODOV, A. V., T. N. MAKSIMOVA, and V. B. MOCHALIN. "ChemInform Abstract: Nitration of Alkyl N-Phenylcarbamates." ChemInform 24, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.199336105.

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9

OHGA, Kazuya, Hiroki OYAMA, and Yoshitaka MUTA. "Chromatographic Optical Resolution on Phenylcarbamates of N-Arylidenechitosans." Analytical Sciences 7, no. 4 (1991): 653–56. http://dx.doi.org/10.2116/analsci.7.653.

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10

NAGAO, Yukinori, Yoshimoto ABE, Takahisa MISONO, et al. "Synthesis and Biological Activities of Phenylcarbamates and Phenylthiocarbamates." NIPPON KAGAKU KAISHI, no. 6 (1993): 719–27. http://dx.doi.org/10.1246/nikkashi.1993.719.

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11

Červinka, Otakar, Anna Fábryová, and Irina Sablukova. "Preparation of secondary alcohols of high optical purity." Collection of Czechoslovak Chemical Communications 51, no. 2 (1986): 401–3. http://dx.doi.org/10.1135/cccc19860401.

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Partially resolved enantiomers of optically active alcohols I-V, obtained by enantioselective reduction of the corresponding ketones with lithium aluminium hydride in the presence of (-)-quinine, were converted into crystalline 3,5-dinitrobenzoates or phenylcarbamates. The esters of the nearly optically pure enantiomers were separated by crystallization from the generally more soluble esters of the racemates. Optical purity of the hydrolytically liberated alcohols was determined by 1H NMR spectroscopy in the presence of chiral shifting agents.

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12

TAKAHASHI, Junya, Shigeko NAKAMURA, Hiroshi NOGUCHI, Toshiro KATO, and Katsuzo KAMOSHITA. "Fungicidal Activity of N-Phenylcarbamates against Benzimidazole Resistant Fungi." Journal of Pesticide Science 13, no. 1 (1988): 63–69. http://dx.doi.org/10.1584/jpestics.13.63.

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13

Zhang, Xiaopeng, Huanzhi Jing, Weiyu Peng, Yafang Li, Xuesen Fan, and Guisheng Zhang. "Selenium-Catalyzed Carbonylation to Phenylcarbamates and Methylene Diphenyl Dicarbamates." Chinese Journal of Organic Chemistry 37, no. 2 (2017): 411. http://dx.doi.org/10.6023/cjoc201609013.

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14

Velikorodov, A. V., V. A. Ionova, E. A. Shustova, and A. A. Starikova. "Synthesis and Antimicrobial Activity of 4-formylphenyl-N-phenylcarbamates." Pharmaceutical Chemistry Journal 50, no. 9 (2016): 583–88. http://dx.doi.org/10.1007/s11094-016-1495-x.

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15

Koh, Han Joong, Ok Sun Kim, Hai Whang Lee, and Ikchoon Lee. "Kinetics and mechanism of the aminolysis ofp-nitrophenylN-phenylcarbamates." Journal of Physical Organic Chemistry 10, no. 10 (1997): 725–30. http://dx.doi.org/10.1002/(sici)1099-1395(199710)10:10<725::aid-poc943>3.0.co;2-x.

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16

Hajinasiri, Rahimeh, and Sobhan Rezayati. "Solvent-free Synthesis of 1,2-Disubstituted Derivatives of 1,2- Dihydroisoquinoline, 1,2-Dihydroquinoline and 1,2-Dihydropyridine." Zeitschrift für Naturforschung B 68, no. 7 (2013): 818–22. http://dx.doi.org/10.5560/znb.2013-3095.

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A one-pot and efficient approach to the synthesis of dialkyl 2-[1-[(alkoxycarbonyl)anilino]-2(1H)- (isoquinolin-2-yl) (or -quinolin-1-yl or -pyridin-1-yl)]-2-butenedioates is described. This method involves a three-component reaction between isoquinoline, quinoline or pyridine, dialkyl acetylenedicarboxylates and N-phenylcarbamates under solvent-free conditions, without using any catalyst and at room temperature. The mild reaction conditions and good yields of the products exhibit the synthetic advantage of this method.

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17

Stankovičová, Mária, and Jozef Čižmárik. "Kinetics of alkaline hydrolysis and correlation studies of m- and p-substituted piperidinoethyl phenylcarbamates." Collection of Czechoslovak Chemical Communications 54, no. 7 (1989): 1846–53. http://dx.doi.org/10.1135/cccc19891846.

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Kinetics of alkaline hydrolysis have been studied with a series of 15 m- and p-substituted piperidinoethyl phenylcarbamates. The rate constants have been determined at 70, 60, 50, and 40 °C and the activation parameters have been calculated. These values have been correlated with the substituent constants σ, F, R, F, R, π. Validity of the Hammett equation and the Swain-Lupton equation has been confirmed in the series studied and for the p-derivatives, respectively. The lipophilicity parameter π does not correlate with the values found.

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18

Ishii, H. "Inheritance of Increased Sensitivity toN-Phenylcarbamates in Benzimidazole-ResistantVenturia nashicola." Phytopathology 78, no. 6 (1988): 695. http://dx.doi.org/10.1094/phyto-78-695.

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19

Mamaeva, A. Elena, S. Saltanat Kaliyeva, A. Abdigali Bakibaev, K. Auezkhan Tashenov, and E. Yenglik Nurpeiis. "A new single-stage method for obtaining of betulin phenylcarbamates." Journal of Asian Natural Products Research 20, no. 12 (2017): 1162–66. http://dx.doi.org/10.1080/10286020.2017.1382480.

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20

VELIKORODOV, A. V., and T. N. MAKSIMOVA. "ChemInform Abstract: Condensation of Aromatic Aldehydes with Methyl N-Phenylcarbamates." ChemInform 29, no. 43 (2010): no. http://dx.doi.org/10.1002/chin.199843102.

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21

Takahashi, Junya, Osamu Kirino, Chiyozo Takayama, et al. "Quantitative structure-activity relationships of the fungicidal methyl N-phenylcarbamates." Pesticide Biochemistry and Physiology 30, no. 3 (1988): 262–71. http://dx.doi.org/10.1016/0048-3575(88)90040-5.

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22

Nalbantova, Didi, Diana Cheshmedzhieva, Boriana Hadjieva, Sonia Ilieva, and Boris Galabov. "Reactivity of phenyl N -phenylcarbamates in the alkaline hydrolysis reaction." Journal of Physical Organic Chemistry 24, no. 12 (2011): 1166–71. http://dx.doi.org/10.1002/poc.1841.

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23

Zahedifar, Mahboobeh, and Hassan Sheibani. "Unexpected Products from Mesoionic 1,3-Thiazinium and Oxazinium Olates: A Novel Access to 3,5-Diaryl-1,3-thiazine-2,4,6-trione and Alkoxy-3,5-diphenyl-3H-1,3-oxazine-2,6-dione Derivatives." Australian Journal of Chemistry 67, no. 9 (2014): 1201. http://dx.doi.org/10.1071/ch14095.

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The condensation of (chlorocarbonyl)ketenes 1 with N-phenylthiocarbamates 2 and N-phenylcarbamates 6 is postulated to lead to the formation of unstable mesoionic 1,3-thiazinium 4-olates I or 1,3-oxazinium 4-olates II, respectively. At room temperature, appropriately substituted mesoionic 1,3-thiazinium 4-olates I eliminated the corresponding alkene with generation of 3,5-diaryl-1,3-thiazine-2,4,6-trione derivatives 3. However, the methoxy-substituted compound 5 was stable at room temperature at least for several weeks. In the case of the mesoionic1,3-oxazinium 4-olates II an alkyl group migrat

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24

Yanosaka, Keiko, Hajime Iwamura, and Toshio Fujita. "Flower Induction in Seedlings of Asparagus officinalis L. by N-Phenylcarbamates." Zeitschrift für Naturforschung C 44, no. 3-4 (1989): 226–32. http://dx.doi.org/10.1515/znc-1989-3-409.

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Abstract A series of N-phenylcarbamates induced flowers in one-month-old seedlings of Asparagus officinalis L. Ninety to 100% of the plants flowered when the seeds were germinated in the presence of the most potent members of this class. The flowering occurred only once at the top of the seedlings, which then continued to grow normally. This made it possible to select the commercially preferred m ales of this dioecious plant at the seedling stage. Both male and female flowers were fertile, so cross-breeding was possible between flowering seedlings as well as between flowering seedlings and ad

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25

Zhao, Xiaodan, Charles S. Yeung, and Vy M. Dong. "Palladium-CatalyzedOrtho-Arylation ofO-Phenylcarbamates with Simple Arenes and Sodium Persulfate." Journal of the American Chemical Society 132, no. 16 (2010): 5837–44. http://dx.doi.org/10.1021/ja100783c.

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26

Zhang, Xiaopeng, Huanzhi Jing, and Guisheng Zhang. "Selenium-Catalyzed Oxidative Carbonylation of Aniline and Alcohols to N-Phenylcarbamates." Synthetic Communications 40, no. 11 (2010): 1614–24. http://dx.doi.org/10.1080/00397910903134626.

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27

Okamoto, Yoshio, Ryo Aburatani, and Koichi Hatada. "Chromatographic Optical Resolution on 3,5-Disubstituted Phenylcarbamates of Cellulose and Amylose." Bulletin of the Chemical Society of Japan 63, no. 3 (1990): 955–57. http://dx.doi.org/10.1246/bcsj.63.955.

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28

PULAVINA, N. N., YU I. DERGUNOV, V. A. IL'IN, and V. F. GEREGA. "ChemInform Abstract: Condensation Reaction of Alkyl N-Phenylcarbamates with Methylating Agents." ChemInform 22, no. 40 (2010): no. http://dx.doi.org/10.1002/chin.199140317.

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29

Chen, Weiwei, Mei Zhang, Ye Feng, et al. "Homogeneous synthesis of partially substituted cellulose phenylcarbamates aiming at chiral recognition." Polymer International 64, no. 8 (2015): 1037–44. http://dx.doi.org/10.1002/pi.4884.

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30

L. Flippen-Anderson, Judith, Xiao-shu He, Arnold Brossi, Nigel H. Greig, and Stanley I. Rapoport. "Thiaphysovenol Phenylcarbamates: X-Ray Structures of Biologically Active and Inactive Anticholinesterase Agents." HETEROCYCLES 36, no. 1 (1993): 79. http://dx.doi.org/10.3987/com-92-6148.

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31

Pietz, Sylke, Dörthe Wölker, and Günter Haufe. "Selectivity of the biooxygenation of N-phenylcarbamates by the fungus Beauveria bassiana." Tetrahedron 53, no. 50 (1997): 17067–78. http://dx.doi.org/10.1016/s0040-4020(97)10148-x.

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32

Fouda, A. S., S. S. Elkaabi, and A. K. Mohamed. "“Substituted phenyl n‐phenylcarbamates as corrosion inhibitors for iron in hydrochloric acid”." Anti-Corrosion Methods and Materials 36, no. 8 (1989): 9–12. http://dx.doi.org/10.1108/eb020787.

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33

Lee, Jae S., Je W. Woo, Chul W. Lee, Ki S. Hong, and Jong K. Yeo. "Selective conversion of nitrobenzene to phenylcarbamates catalyzed by Pd(II) and heteropolyacids." Korean Journal of Chemical Engineering 7, no. 2 (1990): 145–47. http://dx.doi.org/10.1007/bf02705060.

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34

Yuan, Hao-Yu, Jun-Chul Choi, Shun-ya Onozawa, et al. "The direct synthesis of N-phenylcarbamates from CO2, aniline, and dibutyltin dialkoxide." Journal of CO2 Utilization 16 (December 2016): 282–86. http://dx.doi.org/10.1016/j.jcou.2016.08.001.

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35

Haufe, Günter, and Dörthe Wölker. "Blocking Fluorine Substitution in Biotransformation of Nortricyclanyl N-Phenylcarbamates with Beauveria bassiana." European Journal of Organic Chemistry 2003, no. 11 (2003): 2159–65. http://dx.doi.org/10.1002/ejoc.200200647.

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36

Shimizu, Ryo, Hajime Iwamura, and Toshio Fujita. "Anticytokinin Activity of N-Phenyl-and N-Pyridylcarbamates." Zeitschrift für Naturforschung C 45, no. 1-2 (1990): 89–95. http://dx.doi.org/10.1515/znc-1990-1-216.

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A new class of non-adenylate anticytokinins, alkyl and phenyl N-phenylcarbamates and related phenyl N-pyridylcarbamates, has been developed. They have a structure that has an immediate resemblance to the non-adenylate class of cytokinins, N ,N′-diphenylureas, and N-pyridyl-N′-phenylureas, and the design of the molecule was made based on insight into the bioisoteric nature between the previous, non-adenylate s-triazine anticytokinins and the carbamate and urea structures. The activity in terms of the I50 value of the most potent members, 4-fluoro- and 4-chlorophenyl N-(2-chloro-4-pyridyl)carbam

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37

Vorčáková, Katarína, Šárka Štěpánková, Miloš Sedlák, and Karel Vytřas. "Electrochemical Sensors for the Estimation of the Inhibitory Effect of Phenylcarbamates to Cholinesterase." Chemosensors 3, no. 4 (2015): 274–83. http://dx.doi.org/10.3390/chemosensors3040274.

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38

Sedlák, Miloš, Jiří Hanusek, Pavel Drabina, Šárka Štěpánková, and Alexander Čegan. "Substituted benzyl N-phenylcarbamates – their solvolysis and inhibition activity to acetylcholinesterase and butyrylcholinesterase." Arkivoc 2009, no. 7 (2009): 1–11. http://dx.doi.org/10.3998/ark.5550190.0010.701.

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39

Bi, Wanying, Fan Wang, Jinhang Han, et al. "Influence of the substituents on phenyl groups on enantioseparation property of amylose phenylcarbamates." Carbohydrate Polymers 241 (August 2020): 116372. http://dx.doi.org/10.1016/j.carbpol.2020.116372.

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40

Zhang, Xiaopeng, Huanzhi Jing, and Guisheng Zhang. "ChemInform Abstract: Selenium-Catalyzed Oxidative Carbonylation of Aniline and Alcohols to N-Phenylcarbamates." ChemInform 41, no. 43 (2010): no. http://dx.doi.org/10.1002/chin.201043076.

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41

KALKOTE, U. R., and N. R. AYYANGAR. "ChemInform Abstract: A Non-Phosgene Route for the Synthesis of Alkyl N-Phenylcarbamates." ChemInform 23, no. 17 (2010): no. http://dx.doi.org/10.1002/chin.199217124.

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42

Šeršeň, František, Katarína Král'ová, and Vendelín Macho. "New Findings about the Inhibitory Action of Phenylcarbamates and Phenylthiocarbamates on Photosynthetic Apparatus." Pesticide Biochemistry and Physiology 68, no. 2 (2000): 113–18. http://dx.doi.org/10.1006/pest.2000.2499.

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43

Adelowo, F. E., I. A. O. Ojo, and O. S. Amuda. "Synthesis and fungicidal activity of some sulphide derivatives of O-phenyl-N-substituted phenylcarbamates." Advances in Biological Chemistry 01, no. 03 (2011): 122–27. http://dx.doi.org/10.4236/abc.2011.13015.

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44

Yamamoto, Chiyo, Tomoko Hayashi, Yoshio Okamoto, and Shiro Kobayashi. "Enantioseparation by Using Chitin Phenylcarbamates as Chiral Stationary Phases for High-Performance Liquid Chromatography." Chemistry Letters 29, no. 1 (2000): 12–13. http://dx.doi.org/10.1246/cl.2000.12.

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45

Kravchenko, Nelly, Elena Nefedeva, Anastasia Timofeeva, Victoria Pleskacheva, and Sergey Belopukhov. "The effect of a new multicomponent herbicide based on phenylcarbamates on sugar beet plants." АгроЭкоИнфо 3, no. 63 (2024): 18. http://dx.doi.org/10.51419/202143318.

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The use of chemical herbicides to control weeds is part of the growing process for most major crops. However, if applied regularly, they can lead to contamination of soil and groundwater, as well as accumulation of residues in crops and the emergence of resistant weed populations. In this regard, it is important to develop environmentally friendly chemical herbicides with new mechanisms of action. Natural phytotoxins of plant or microbial origin can serve as prototypes of active substances. The article discusses the following aspects: 1) the relevance of the topic of the impact of herbicides o

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46

VELIKORODOV, A. V. "ChemInform Abstract: Synthesis and Conversion of Chloromethylation Products of p-Substituted Methyl N-Phenylcarbamates." ChemInform 29, no. 43 (2010): no. http://dx.doi.org/10.1002/chin.199843100.

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47

PIETZ, S., D. WOELKER, and G. HAUFE. "ChemInform Abstract: Selectivity of the Biooxygenation of N-Phenylcarbamates by the Fungus Beauveria bassiana." ChemInform 29, no. 15 (2010): no. http://dx.doi.org/10.1002/chin.199815028.

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48

GREGAN, F., V. KETTMANN, P. NOVOMESKY, E. POLASEK, and J. SIVY. "ChemInform Abstract: Synthesis and Local Anesthetic Activity of Two Homological Series of Diastereomeric Phenylcarbamates." ChemInform 27, no. 22 (2010): no. http://dx.doi.org/10.1002/chin.199622114.

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49

Haufe, Günter, Sylke Pietz, Dörthe Wölker, and Roland Fröhlich. "Synthesis of Fluorinated Cycloalkyl N-Phenylcarbamates and Their Microbial Defluorination/Oxygenation by Beauveria bassiana." European Journal of Organic Chemistry 2003, no. 11 (2003): 2166–75. http://dx.doi.org/10.1002/ejoc.200200648.

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50

Ma, Huijun, Tao Wang, Chenying Gao, Guangshen Li, Minghao Zhang, and Qifeng Wang. "Pd(ii)/Ag(i)-Cocatalyzed ortho direct arylation of O-phenylcarbamates with pinacol aryl boronates." Organic Chemistry Frontiers 6, no. 9 (2019): 1409–13. http://dx.doi.org/10.1039/c9qo00227h.

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