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Статті в журналах з теми "Dithiocarboxylic acids"

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Автор: Grafiati

Опубліковано: 18 травня 2024

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1

R. Katritzky, Alan, Charles M. Marson, and Hassan Faid-Allah. "Heterocyclic N-Dithiocarboxylic Acids." HETEROCYCLES 26, no. 6 (1987): 1657. http://dx.doi.org/10.3987/r-1987-06-1657.

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2

Petrova, R. G., T. D. Churkina, I. I. Kandror, V. I. Dostovalova, and R. Kh Freidlina. "Radical arylation of esters of dithiocarboxylic acids." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 11 (November 1985): 2331–36. http://dx.doi.org/10.1007/bf00956795.

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3

Drozd, V. N. "The Pericyclic Reaction of the Derivatives of Dithiocarboxylic Acids." Phosphorus, Sulfur, and Silicon and the Related Elements 58, no. 1-4 (April 1991): 255–73. http://dx.doi.org/10.1080/10426509108040634.

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4

Lee, Tai-Chou, Pei-Chun Chen, Ting-Ying Lai, Wirote Tuntiwechapikul, Jun-Hyun Kim, and T. Randall Lee. "Aliphatic dithiocarboxylic acids: New adsorbates for soft lithographic patterning." Applied Surface Science 254, no. 21 (August 2008): 7064–68. http://dx.doi.org/10.1016/j.apsusc.2008.05.192.

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5

Colorado, Ramon, Ramon J. Villazana, and T. Randall Lee. "Self-Assembled Monolayers on Gold Generated from Aliphatic Dithiocarboxylic Acids." Langmuir 14, no. 22 (October 1998): 6337–40. http://dx.doi.org/10.1021/la9804381.

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6

Churkina, T. D., R. G. Petrova, and R. Kh Freidlina. "Reaction of butyl mercaptan with phenyl esters of dithiocarboxylic acids." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 37, no. 12 (December 1988): 2562–64. http://dx.doi.org/10.1007/bf00952641.

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7

DROZD, V. N. "ChemInform Abstract: Pericyclic Reaction of the Derivatives of Dithiocarboxylic Acids." ChemInform 22, no. 35 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199135312.

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8

DOELLING, W., I. HOCKE, P. VERJUS, M. BIEDERMANN, and H. HARTUNG. "ChemInform Abstract: Enantiomeric and Diastereomeric Esters of 2-Methoxymethylpyrrolidine-1-dithiocarboxylic Acids." ChemInform 28, no. 48 (August 2, 2010): no. http://dx.doi.org/10.1002/chin.199748147.

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9

Kato, Shinzi, Akira Hori, Masateru Mitsuta, Tomonori Katada, Hideharu Ishihara, Kunimi Fujieda, and Yoshinori Ikebe. "On carbon-13 spectra of thio- and dithiocarboxylic acids triorgano group 14 metal esters." Journal of Organometallic Chemistry 420, no. 1 (November 1991): 13–22. http://dx.doi.org/10.1016/0022-328x(91)86440-2.

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10

Grote, Johanna, Felix Friedrich, Katarína Berthold, Loreen Hericks, Beate Neumann, Hans-Georg Stammler, and Norbert W. Mitzel. "Dithiocarboxylic Acids: An Old Theme Revisited and Augmented by New Preparative, Spectroscopic and Structural Facts." Chemistry - A European Journal 24, no. 11 (January 31, 2018): 2626–33. http://dx.doi.org/10.1002/chem.201704235.

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11

Bonnans-Plaisance, C., and G. Levesque. "Homo- and copolymerization of unprotected 2-(hydroxymethyl)thiirane initiated by quaternary ammonium salts of dithiocarboxylic acids." Macromolecules 22, no. 4 (July 1989): 2020–23. http://dx.doi.org/10.1021/ma00194a088.

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12

Chiacchio, Maria-Assunta, Laura Legnani, Pierluigi Caramella, Tomás Tejero, and Pedro Merino. "Revealing carbocations in highly asynchronous concerted reactions: The ene-type reaction between dithiocarboxylic acids and alkenes." Tetrahedron 74, no. 39 (September 2018): 5627–34. http://dx.doi.org/10.1016/j.tet.2018.07.056.

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13

Yamamoto, Tatsuo, Shigeo Hirasawa та Motomu Muraoka. "Synthesis of β-Alkylimino α-Cyano Dithiocarboxylic Acids, 3-Alkyl-1,3-thiazine-2,6-dithiones, and Related Compounds". Bulletin of the Chemical Society of Japan 58, № 2 (лютий 1985): 771–72. http://dx.doi.org/10.1246/bcsj.58.771.

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14

V. Magedov, Igor, Sergey Yu. Shapakin, and Victor N. Drozd. "The reaction of allylic esters of dithiocarboxylic acids with tetracyanoethylene affording 3,3,4,4-tetracyano-6,8-dithiabicyclo[3.2.1]octanes." Tetrahedron 51, no. 42 (October 1995): 11503–14. http://dx.doi.org/10.1016/0040-4020(95)00739-u.

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15

Pikun, Nadiia V., Sergiy S. Mykhaylychenko та Yuriy G. Shermolovich. "The synthesis of fluorine-containing endothiopeptide analogs by the reaction of perfluorinated dithiocarboxylic acids amides with esters of α-amino acids and dipeptides". Arkivoc 2018, № 3 (29 листопада 2017): 36–44. http://dx.doi.org/10.24820/ark.5550190.p010.305.

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16

Cimatu, Katherine, H. Justin Moore, T. Randall Lee, and Steven Baldelli. "Sum Frequency Generation Imaging of Microcontact-Printed Monolayers Derived from Aliphatic Dithiocarboxylic Acids: Contrast Based on Terminal-Group Orientation." Journal of Physical Chemistry C 111, no. 32 (July 24, 2007): 11751–55. http://dx.doi.org/10.1021/jp0746493.

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17

Kanagasabapathy, Subbareddy, Arumugam Sudalai, and Brian C. Benicewicz. "Montmorillonite K 10-catalyzed regioselective addition of thiols and thiobenzoic acids onto olefins: an efficient synthesis of dithiocarboxylic esters." Tetrahedron Letters 42, no. 23 (June 2001): 3791–94. http://dx.doi.org/10.1016/s0040-4039(01)00570-6.

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18

MAGEDOV, I. V., S. YU SHAPAKIN, and V. N. DROZD. "ChemInform Abstract: The Reaction of Allylic Esters of Dithiocarboxylic Acids with Tetracyanoethylene Affording 3,3,4,4-Tetracyano-6,8-dithiabicyclo(3.2. 1)octanes." ChemInform 27, no. 9 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.199609052.

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19

Safavi, Afsaneh, and Lida Fotouhi. "Spectrophotometric Determination of Stability Constants of Ni(II) and Ag(I) Complexes with Some Dithiocarboxylic Acids in Dimethylsulfoxide–Water Mixtures." Microchemical Journal 59, no. 3 (July 1998): 351–55. http://dx.doi.org/10.1006/mchj.1998.1603.

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20

Kanagasabapathy, Subbareddy, Arumugam Sudalai, and Brian C. Benicewicz. "ChemInform Abstract: Montmorillonite K 10 Catalyzed Regioselective Addition of Thiols and Thiobenzoic Acids onto Olefins: An Efficient Synthesis of Dithiocarboxylic Esters." ChemInform 32, no. 35 (May 24, 2010): no. http://dx.doi.org/10.1002/chin.200135046.

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21

KOESTER, R., R. KUCZNIERZ, G. SEIDEL, and P. BETZ. "ChemInform Abstract: Boron Compounds. Part 104. Dithiocarboxylic Acids and Derivatives from Carboxylic Esters and Lactones with the Organoboron Sulfide Reagent (9- BBN)2S." ChemInform 23, no. 34 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199234199.

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22

Chaudhury, Muktimoy. "Chemistry of molybdenum. 4. Complexes of molybdenum(VI), -(V) and -(IV) with 2-(alkylamino)cyclopent-1-ene-1-dithiocarboxylic acids. Synthesis, electrochemistry and spectroscopic properties." Inorganic Chemistry 24, no. 19 (September 1985): 3011–17. http://dx.doi.org/10.1021/ic00213a028.

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23

Sychyeva, Ye S., and M. S. Mukanova. "SYNTHESIS AND CHEMICAL MODIFICATION OF NEW HYDROXYBEZALDEHYDE DERIVATIVES." Chemical Journal of Kazakhstan, no. 3 (September 15, 2023): 127–36. http://dx.doi.org/10.51580/2023-3.2710-1185.34.

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Анотація:

A high pharmacological ability of aromatic benzaldehydes makes them important intermediates for the synthesis of medicinal preparations, such as anticancer, bactericidal, antifungal, and herbicidal drugs. The purpose of this work is the synthesis of biologically active compounds, based on 4-hydroxybenzaldehyde and 4-hydroxy-3-methoxybenzaldehyde and the establishment of the structure of the synthesized compounds. Results and discussion. New carbonodithioates, based on O-aromatic systems have been synthesized by the interaction of 4-hydroxybenzaldehyde and 4-hydroxy-3-methoxybenzaldehyde with carbon disulfide in the presence of sodium hydroxide in ethanol at the room temperature. As a result of the reactions, sodium O-(4-formylphenyl)carbodithioate (86 %) and sodium O-(4-formyl-2-methoxyphenyl)carbodithioate (80%) have been isolated. The interaction of sodium xanthates with acid chlorides (4-methoxy-, 4-nitro-, 2,4-dinitrobenzoic) in chloroform has led to the formation of aromatic thioanhydrides of carbonodithioic acids in 55-80 % yields. The reactivity of hydroxybenzaldehydes and their dithiocarboxylic derivatives has been studied in the propargylation reaction. Propargylation of 4-hydroxybenzaldehyde and 4-hydroxy-3-methoxybenzaldehyde has been carried out with propargyl bromide in the presence of a 3-fold excess of K2CO3 in acetone at the temperature of 60°C. The propargylation reaction of sodium xanthate has been carried out with propargyl bromide in acetone at the room temperature. Conclusion. As a result of the reactions, carbonodithioates, thioanhydrides, acetylenic and thioacetylenic ethers have been synthesized based, on O-aromatic systems (4-hydroxybenzaldehyde and 4-hydroxy-3-methoxybenzaldehyde). The structure of the synthesized compounds has been established on the basis of elemental analysis data, IR spectra, 1Н and 13С NMR spectroscopy.

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24

KATRITZKY, A. R., C. M. MARSON, and H. FAID-ALLAH. "ChemInform Abstract: Heterocyclic N-Dithiocarboxylic Acids." ChemInform 18, no. 51 (December 22, 1987). http://dx.doi.org/10.1002/chin.198751390.

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25

THIEL, W., and R. MAYER. "ChemInform Abstract: Dithiocarboxylic Acids, Dithiocarboxylic Esters, or Thiocarboxylic Amides by Reaction of Methylene-Active Chloromethyl Compounds with Sulfur." ChemInform 21, no. 1 (January 2, 1990). http://dx.doi.org/10.1002/chin.199001096.

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26

STEPANOVA, N. P., N. YA KUZ'MINA, E. S. TURBANOVA, and M. L. PETROV. "ChemInform Abstract: Reaction of the Salts of Dithiocarboxylic Acids with Trifluoromethylacetylene and Trifluoromethylalkyldiynes." ChemInform 18, no. 7 (February 17, 1987). http://dx.doi.org/10.1002/chin.198707135.

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27

Shon, Young-Seok, Nupur Garg, Ramon Colorado, Ramon J. Villazana, and T. Randall Lee. "Self-Assembled Monolayers Derived from Bidentate Organosulfur Adsorbates." MRS Proceedings 576 (1999). http://dx.doi.org/10.1557/proc-576-183.

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Анотація:

ABSTRACTThe adsorption of a series of 1,2-bis(mercaptomethyl)-4,5-dialkylbenzenes (1), spiroalkanedithiols (2), and aliphatic dithiocarboxylic acids (3) on gold yielded new types of self-assembled monolayers (SAMs). The new SAMs were characterized by optical ellipsometry, contact angle goniometry, and polarization modulation infrared reflection absorption spectroscopy (PM-IRRAS). These results were compared to those obtained from SAMs derived from normal alkanethiols (4) of analogous chain length. Comparisons of ellipsometric thickness and contact angle wettability showed that the new SAMs were well packed and highly oriented. Comparisons of the PM-IRRAS data showed that the SAMs generated from 1 and 2 exhibited slightly less crystallinity than their alkanethiolate-based analogs, while the SAMs generated from 3 exhibited comparable crystallinity to their alkanethiolate-based analogs. Moreover, the SAMs derived from 1 and 2 showed no “odd-even” wettability or PM-IRRAS effects, while those derived from 3 showed remarkably large “odd-even” effects compared to those derived from normal alkanethiols.

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28

YAMAMOTO, T., S. HIRASAWA та M. MURAOKA. "ChemInform Abstract: SYNTHESIS OF β-(ALKYLIMINO) α-CYANO DITHIOCARBOXYLIC ACIDS, 3-ALKYL-1,3-THIAZINE-2,6-DITHIONES, AND RELATED COMPOUNDS". Chemischer Informationsdienst 16, № 32 (13 серпня 1985). http://dx.doi.org/10.1002/chin.198532233.

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29

CHAUDHURY, M. "ChemInform Abstract: CHEMISTRY OF MOLYBDENUM. 4. COMPLEXES OF MOLYBDENUM(VI), -(V) AND -(IV) WITH 2-(ALKYLAMINO)CYCLOPENT-1-ENE-1-DITHIOCARBOXYLIC ACIDS. SYNTHESIS, ELECTROCHEMISTRY AND SPECTROSCOPIC PROPERTIES." Chemischer Informationsdienst 16, no. 51 (December 24, 1985). http://dx.doi.org/10.1002/chin.198551265.

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