Bibliografías temáticas / Dithiocarboxylic acids / Artículos de revistas

Artículos de revistas sobre el tema "Dithiocarboxylic acids"

Siga este enlace para ver otros tipos de publicaciones sobre el tema: Dithiocarboxylic acids.
Autor: Grafiati
Publicado: 18 de mayo de 2024

Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros

Elija tipo de fuente:

Consulte los 29 mejores artículos de revistas para su investigación sobre el tema "Dithiocarboxylic acids".

Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.

También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.

Explore artículos de revistas sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.

1

R. Katritzky, Alan, Charles M. Marson y Hassan Faid-Allah. "Heterocyclic N-Dithiocarboxylic Acids". HETEROCYCLES 26, n.º 6 (1987): 1657. http://dx.doi.org/10.3987/r-1987-06-1657.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
2

Petrova, R. G., T. D. Churkina, I. I. Kandror, V. I. Dostovalova y R. Kh Freidlina. "Radical arylation of esters of dithiocarboxylic acids". Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, n.º 11 (noviembre de 1985): 2331–36. http://dx.doi.org/10.1007/bf00956795.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
3

Drozd, V. N. "The Pericyclic Reaction of the Derivatives of Dithiocarboxylic Acids". Phosphorus, Sulfur, and Silicon and the Related Elements 58, n.º 1-4 (abril de 1991): 255–73. http://dx.doi.org/10.1080/10426509108040634.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
4

Lee, Tai-Chou, Pei-Chun Chen, Ting-Ying Lai, Wirote Tuntiwechapikul, Jun-Hyun Kim y T. Randall Lee. "Aliphatic dithiocarboxylic acids: New adsorbates for soft lithographic patterning". Applied Surface Science 254, n.º 21 (agosto de 2008): 7064–68. http://dx.doi.org/10.1016/j.apsusc.2008.05.192.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
5

Colorado, Ramon, Ramon J. Villazana y T. Randall Lee. "Self-Assembled Monolayers on Gold Generated from Aliphatic Dithiocarboxylic Acids". Langmuir 14, n.º 22 (octubre de 1998): 6337–40. http://dx.doi.org/10.1021/la9804381.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
6

Churkina, T. D., R. G. Petrova y 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, n.º 12 (diciembre de 1988): 2562–64. http://dx.doi.org/10.1007/bf00952641.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
7

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

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
8

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

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
9

Kato, Shinzi, Akira Hori, Masateru Mitsuta, Tomonori Katada, Hideharu Ishihara, Kunimi Fujieda y Yoshinori Ikebe. "On carbon-13 spectra of thio- and dithiocarboxylic acids triorgano group 14 metal esters". Journal of Organometallic Chemistry 420, n.º 1 (noviembre de 1991): 13–22. http://dx.doi.org/10.1016/0022-328x(91)86440-2.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
10

Grote, Johanna, Felix Friedrich, Katarína Berthold, Loreen Hericks, Beate Neumann, Hans-Georg Stammler y Norbert W. Mitzel. "Dithiocarboxylic Acids: An Old Theme Revisited and Augmented by New Preparative, Spectroscopic and Structural Facts". Chemistry - A European Journal 24, n.º 11 (31 de enero de 2018): 2626–33. http://dx.doi.org/10.1002/chem.201704235.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
11

Bonnans-Plaisance, C. y G. Levesque. "Homo- and copolymerization of unprotected 2-(hydroxymethyl)thiirane initiated by quaternary ammonium salts of dithiocarboxylic acids". Macromolecules 22, n.º 4 (julio de 1989): 2020–23. http://dx.doi.org/10.1021/ma00194a088.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
12

Chiacchio, Maria-Assunta, Laura Legnani, Pierluigi Caramella, Tomás Tejero y Pedro Merino. "Revealing carbocations in highly asynchronous concerted reactions: The ene-type reaction between dithiocarboxylic acids and alkenes". Tetrahedron 74, n.º 39 (septiembre de 2018): 5627–34. http://dx.doi.org/10.1016/j.tet.2018.07.056.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
13

Yamamoto, Tatsuo, Shigeo Hirasawa y 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, n.º 2 (febrero de 1985): 771–72. http://dx.doi.org/10.1246/bcsj.58.771.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
14

V. Magedov, Igor, Sergey Yu. Shapakin y 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, n.º 42 (octubre de 1995): 11503–14. http://dx.doi.org/10.1016/0040-4020(95)00739-u.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
15

Pikun, Nadiia V., Sergiy S. Mykhaylychenko y 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, n.º 3 (29 de noviembre de 2017): 36–44. http://dx.doi.org/10.24820/ark.5550190.p010.305.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
16

Cimatu, Katherine, H. Justin Moore, T. Randall Lee y 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, n.º 32 (24 de julio de 2007): 11751–55. http://dx.doi.org/10.1021/jp0746493.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
17

Kanagasabapathy, Subbareddy, Arumugam Sudalai y 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, n.º 23 (junio de 2001): 3791–94. http://dx.doi.org/10.1016/s0040-4039(01)00570-6.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
18

MAGEDOV, I. V., S. YU SHAPAKIN y 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, n.º 9 (12 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199609052.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
19

Safavi, Afsaneh y 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, n.º 3 (julio de 1998): 351–55. http://dx.doi.org/10.1006/mchj.1998.1603.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
20

Kanagasabapathy, Subbareddy, Arumugam Sudalai y 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, n.º 35 (24 de mayo de 2010): no. http://dx.doi.org/10.1002/chin.200135046.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
21

KOESTER, R., R. KUCZNIERZ, G. SEIDEL y 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, n.º 34 (21 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199234199.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
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, n.º 19 (septiembre de 1985): 3011–17. http://dx.doi.org/10.1021/ic00213a028.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
23

Sychyeva, Ye S. y M. S. Mukanova. "SYNTHESIS AND CHEMICAL MODIFICATION OF NEW HYDROXYBEZALDEHYDE DERIVATIVES". Chemical Journal of Kazakhstan, n.º 3 (15 de septiembre de 2023): 127–36. http://dx.doi.org/10.51580/2023-3.2710-1185.34.

Texto completo
Resumen
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.
Los estilos APA, Harvard, Vancouver, ISO, etc.
24

KATRITZKY, A. R., C. M. MARSON y H. FAID-ALLAH. "ChemInform Abstract: Heterocyclic N-Dithiocarboxylic Acids". ChemInform 18, n.º 51 (22 de diciembre de 1987). http://dx.doi.org/10.1002/chin.198751390.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
25

THIEL, W. y R. MAYER. "ChemInform Abstract: Dithiocarboxylic Acids, Dithiocarboxylic Esters, or Thiocarboxylic Amides by Reaction of Methylene-Active Chloromethyl Compounds with Sulfur." ChemInform 21, n.º 1 (2 de enero de 1990). http://dx.doi.org/10.1002/chin.199001096.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
26

STEPANOVA, N. P., N. YA KUZ'MINA, E. S. TURBANOVA y M. L. PETROV. "ChemInform Abstract: Reaction of the Salts of Dithiocarboxylic Acids with Trifluoromethylacetylene and Trifluoromethylalkyldiynes." ChemInform 18, n.º 7 (17 de febrero de 1987). http://dx.doi.org/10.1002/chin.198707135.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
27

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

Texto completo
Resumen
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.
Los estilos APA, Harvard, Vancouver, ISO, etc.
28

YAMAMOTO, T., S. HIRASAWA y 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, n.º 32 (13 de agosto de 1985). http://dx.doi.org/10.1002/chin.198532233.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
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, n.º 51 (24 de diciembre de 1985). http://dx.doi.org/10.1002/chin.198551265.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
Ofrecemos descuentos en todos los planes premium para autores cuyas obras están incluidas en selecciones literarias temáticas. ¡Contáctenos para obtener un código promocional único!

Pasar a la bibliografía