Gotowe bibliografie tematyczne / Versatile intermediates / Artykuły w czasopismach
Kliknij ten link, aby zobaczyć inne rodzaje publikacji na ten temat: Versatile intermediates.

Artykuły w czasopismach na temat „Versatile intermediates”

Autor: Grafiati
Data publikacji: 6 września 2023

Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych

Wybierz rodzaj źródła:

Sprawdź 50 najlepszych artykułów w czasopismach naukowych na temat „Versatile intermediates”.

Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.

Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.

Przeglądaj artykuły w czasopismach z różnych dziedzin i twórz odpowiednie bibliografie.

1

Boeske, Juergen, Edgar Niecke, Edgar Ocando-Mavarez, Jean Pierre Majoral i Guy Bertrand. "Phosphonitriles: versatile intermediates". Inorganic Chemistry 25, nr 16 (lipiec 1986): 2695–98. http://dx.doi.org/10.1021/ic00236a008.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Belletire, J. L. "Acylcyanamides: Versatile Synthetic Intermediates". Synthetic Communications 18, nr 16-17 (listopad 1988): 2063–71. http://dx.doi.org/10.1080/00397918808068275.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

R. Katritzky, Alan, Adam S. Vincek i Peter J. Steel. "Triphenylphosphoranylidene Substituted Heterocycles as Versatile Intermediates". HETEROCYCLES 76, nr 2 (2008): 1401. http://dx.doi.org/10.3987/com-08-s(f)12.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Britten, Thomas K., Paul D. Kemmitt, Nathan R. Halcovitch i Susannah C. Coote. "1,2-Dihydropyridazines as Versatile Synthetic Intermediates". Synlett 31, nr 05 (13.02.2020): 459–62. http://dx.doi.org/10.1055/s-0039-1690825.

Pełny tekst źródła
Streszczenie:
The reactivity of 1,2-dihydropyridazines under various conditions is described, leading to the formation of a variety of products, including 2-aminopyrroles, phenylenediamines, and several novel heterocyclic motifs.
Style APA, Harvard, Vancouver, ISO itp.
5

Bari, Ahmed. "Monosaccharidic Push-pull Butadienes: Versatile Synthetic Intermediates". Zeitschrift für Naturforschung B 69, nr 1 (1.01.2014): 98–102. http://dx.doi.org/10.5560/znb.2014-3179.

Pełny tekst źródła
Streszczenie:
Monosaccharidic push-pull butadienes are interesting building blocks for the synthesis of various heterocyclic and natural products due to their biological prevalence and significant p-electron interactions between donor and acceptor groups. A series of 1,5-anhydro-3,4,6-tri-O-benzyl-2-deoxy- 2-formyl-D-arabino-hex-1-enitol (2) and 1,5-anhydro-3,4-di-O-benzyl-2-deoxy-2-formyl-L-erythrohex- 1-enitol (4) derived push-pull branched chain sugars have been synthesized by condensation with active methylene compounds using basic aluminum oxide (Al2O3) or anhydrous sodium acetate (NaOAc) at room temperature. The compounds have been fully characterized by spectroscopic techniques and elemental analyses.
Style APA, Harvard, Vancouver, ISO itp.
6

Attanasi, Orazio A., i Luciano Caglioti. "CONJUGATED AZOALKENES: ATTRACTIVE PRODUCTS AND VERSATILE INTERMEDIATES". Organic Preparations and Procedures International 18, nr 5 (październik 1986): 299–327. http://dx.doi.org/10.1080/00304948609356836.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

Flashman, Emily, i Christopher J. Schofield. "The most versatile of all reactive intermediates?" Nature Chemical Biology 3, nr 2 (luty 2007): 86–87. http://dx.doi.org/10.1038/nchembio0207-86.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Zellner, Armin, i Manfred Schlosser. "Pentadienyltitaniums as Versatile Intermediates: Regio- and Stereoselectivities". Synlett 2001, Special Issue (2001): 1016–18. http://dx.doi.org/10.1055/s-2001-14650.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Barrett, Anthony G. M., i Gregory G. Graboski. "Conjugated nitroalkenes: versatile intermediates in organic synthesis". Chemical Reviews 86, nr 5 (październik 1986): 751–62. http://dx.doi.org/10.1021/cr00075a002.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Michael, J. P., C. B. de Koning, D. Gravestock, G. D. Hosken, A. S. Howard, C. M. Jungmann, R. W. M. Krause, A. S. Parsons, S. C. Pelly i T. V. Stanbury. "Enaminones: versatile intermediates for natural product synthesis". Pure and Applied Chemistry 71, nr 6 (30.06.1999): 979–88. http://dx.doi.org/10.1351/pac199971060979.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
11

Joergensen, M., K. A. Lerstrup i K. Bechgaard. "Mesoions as versatile intermediates in tetrathiafulvalene synthesis". Journal of Organic Chemistry 56, nr 19 (wrzesień 1991): 5684–88. http://dx.doi.org/10.1021/jo00019a041.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
12

Chemla, Fabrice. "α-Oxy sulfones and sulfoximines: versatile intermediates". Journal of the Chemical Society, Perkin Transactions 1, nr 3 (10.01.2002): 275–99. http://dx.doi.org/10.1039/b009523k.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
13

Lamberth, Clemens. "Organic Isocyanates and Isothiocyanates: Versatile Intermediates in Agrochemistry". Synthesis 54, nr 05 (26.10.2021): 1250–60. http://dx.doi.org/10.1055/a-1678-8528.

Pełny tekst źródła
Streszczenie:
AbstractIn recent decades, organic isocyanates and isothiocyanates have been often applied as reactive intermediates in research syntheses or manufacturing routes of many agrochemicals. These heterocumulenes allowed the installation of crucial carboxylic functions, such as carbamates, ureas, and semicarbazones, but have also been used for the construction of five- and six-membered heterocycles, such as tetrazolones, thiazoles, and uracils.1 Introduction2 Preparation of Carboxylic Acid Functions3 Preparation of Heterocyclic Rings4 Conclusion
Style APA, Harvard, Vancouver, ISO itp.
14

Warkentin, John. "Δ3-1,3,4-Oxadiazolines.† Versatile sources of reactive intermediates". Journal of the Chemical Society, Perkin Transactions 1, nr 14 (2000): 2161–69. http://dx.doi.org/10.1039/b000930j.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
15

Redely, D. Bhaskar, M. V. Ramana Redely i V. Padmavathi. "Cyclohexanone Gem-Dicarboxylates - Versatile Intermediates for Fused Heterocycles". Synthetic Communications 29, nr 4 (luty 1999): 667–76. http://dx.doi.org/10.1080/00397919908085815.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
16

Havel, Václav, Tereza Sadilová i Vladimír Šindelář. "Unsubstituted Bambusurils: Post-Macrocyclization Modification of Versatile Intermediates". ACS Omega 3, nr 4 (27.04.2018): 4657–63. http://dx.doi.org/10.1021/acsomega.8b00497.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
17

Krafft, Grant A., Ester A. Garcia, Anil Guram, Brian O'Shaughnessy i Xialong Xu. "Simplified cytochalasins. 1. Synthesis of versatile perhydroisoindolone intermediates." Tetrahedron Letters 27, nr 24 (1986): 2691–94. http://dx.doi.org/10.1016/s0040-4039(00)84618-3.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
18

van de Wouw, Heidi L., i Rebekka S. Klausen. "BN Polystyrenes: Emerging Optical Materials and Versatile Intermediates". Journal of Organic Chemistry 84, nr 3 (8.01.2019): 1117–25. http://dx.doi.org/10.1021/acs.joc.8b02921.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
19

Irwin, Jacob L., i Michael S. Sherburn. "Monolithiocavitands: Versatile Intermediates for New Cavitand-Based Hosts". Organic Letters 3, nr 2 (styczeń 2001): 225–27. http://dx.doi.org/10.1021/ol006881w.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
20

Waldvogel, Siegfried R., i Sabine Möhle. "Versatile Electrochemical CH Amination via Zincke Intermediates". Angewandte Chemie International Edition 54, nr 22 (12.05.2015): 6398–99. http://dx.doi.org/10.1002/anie.201502638.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
21

Zhang, Shu Xin. "Research on Synthesis of Benzoic Acids Intermediates". Applied Mechanics and Materials 192 (lipiec 2012): 270–74. http://dx.doi.org/10.4028/www.scientific.net/amm.192.270.

Pełny tekst źródła
Streszczenie:
This article briefly describes the development of dye intermediates in China and the research and development situation on synthetic 2 - amino-5 - nitrobenzoic acids. It also tries two more new routes to practice synthesis of them, for which it focuses on speculation of the reaction mechanism of the former route and on research of process conditions of the latter, getting the optimal conditions of the synthetic 5 - nitro-isatin. 2 - Amino - 5 - nitro benzoic acid is a versatile organic intermediate, which is seldom reported both home and abroad, but research on its synthesis method and process conditions are significant to the development of China's fine intermediates industry.
Style APA, Harvard, Vancouver, ISO itp.
22

Roy, Tony, i Akkattu T. Biju. "Recent advances in molecular rearrangements involving aryne intermediates". Chemical Communications 54, nr 21 (2018): 2580–94. http://dx.doi.org/10.1039/c7cc09122b.

Pełny tekst źródła
Streszczenie:
A concise account on the recent developments in molecular rearrangements proceeding via the aryne intermediate is presented thereby shedding light on the synthetic potential of this versatile intermediate.
Style APA, Harvard, Vancouver, ISO itp.
23

Ducrot, Paul-Henri, Anne-Claire Hervier i Jean-Yves Lallemand. "Stereoselective Synthesis of Versatile Intermediates for Clerodanes Total synthesis". Synthetic Communications 26, nr 23 (grudzień 1996): 4447–57. http://dx.doi.org/10.1080/00397919608003847.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
24

Cordero, Franca M., Francesco De Sarlo i Alberto Brandi. "5-Spirocyclopropane Isoxazolidines as Versatile Intermediates in Organic Synthesis". Monatshefte f�r Chemie / Chemical Monthly 135, nr 6 (1.06.2004): 649–69. http://dx.doi.org/10.1007/s00706-003-0150-x.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
25

Mukaiyama, Teruaki, i Hokuto Yamabe. "Alkyl Phosphinites: Versatile Synthetic Intermediates for Dehydration Condensation Reactions". Chemistry Letters 36, nr 1 (styczeń 2007): 2–7. http://dx.doi.org/10.1246/cl.2007.2.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
26

Schmidt, Richard R. "Functionally Substituted Vinyl Carbanions Versatile Intermediates in Heterocyclic Synthesis". Bulletin des Sociétés Chimiques Belges 92, nr 9 (1.09.2010): 825–36. http://dx.doi.org/10.1002/bscb.19830920909.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
27

Michael, Joseph P., Charles B. De Koning, David Gravestock, Gladys D. Hosken, Arthur S. Howard, Christa M. Jungmann, Rui W. M. Krause, Andrew S. Parsons, Stephen C. Pelly i Trevor V. Stanbury. "ChemInform Abstract: Enaminones: Versatile Intermediates for Natural Product Synthesis". ChemInform 31, nr 4 (11.06.2010): no. http://dx.doi.org/10.1002/chin.200004280.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
28

Zellner, Armin, i Manfred Schlosser. "ChemInform Abstract: Pentadienyltitaniums as Versatile Intermediates: Regio- and Stereoselectivities." ChemInform 32, nr 40 (24.05.2010): no. http://dx.doi.org/10.1002/chin.200140064.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
29

JOERGENSEN, M., K. A. LERSTRUP i K. BECHGAARD. "ChemInform Abstract: Mesoions as Versatile Intermediates in Tetrathiafulvalene Synthesis." ChemInform 23, nr 6 (22.08.2010): no. http://dx.doi.org/10.1002/chin.199206174.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
30

Chemla, Fabrice. "ChemInform Abstract: α-Oxy Sulfones and Sulfoximines: Versatile Intermediates". ChemInform 33, nr 24 (21.05.2010): no. http://dx.doi.org/10.1002/chin.200224251.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
31

Evano, Gwilherm, Morgan Lecomte, Pierre Thilmany i Cédric Theunissen. "Keteniminium Ions: Unique and Versatile Reactive Intermediates for Chemical Synthesis". Synthesis 49, nr 15 (17.07.2017): 3183–214. http://dx.doi.org/10.1055/s-0036-1588452.

Pełny tekst źródła
Streszczenie:
Keteniminium ions have been demonstrated to be remarkably useful and versatile reactive intermediates in chemical synthesis. These unique heterocumulenes are pivotal electrophilic species involved in a number of efficient and selective transformations. More recently, even more reactive ‘activated’ keteniminium ions bearing an additional electron-withdrawing group on the nitrogen atom have been extensively investigated. The chemistry of these unique reactive intermediates, including representative methods for their in situ generation, will be overviewed in this review article.1 Introduction2 The Chemistry of Keteniminium Ions3 The Chemistry of Activated Keteniminium Ions4 Keteniminium Ions: Pivotal Intermediates for the Synthesis of Natural and/or Biologically Relevant Molecules5 Conclusions and Perspectives
Style APA, Harvard, Vancouver, ISO itp.
32

Tian, Feitao, Guobing Yan i Jian Yu. "Recent advances in the synthesis and applications of α-(trifluoromethyl)styrenes in organic synthesis". Chemical Communications 55, nr 90 (2019): 13486–505. http://dx.doi.org/10.1039/c9cc06465f.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
33

Iwanejko, Jakub, i Elżbieta Wojaczyńska. "Cyclic imines – preparation and application in synthesis". Organic & Biomolecular Chemistry 16, nr 40 (2018): 7296–314. http://dx.doi.org/10.1039/c8ob01874j.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
34

Dong, Kuiyong, Mengting Liu i Xinfang Xu. "Recent Advances in Catalytic Alkyne Transformation via Copper Carbene Intermediates". Molecules 27, nr 10 (11.05.2022): 3088. http://dx.doi.org/10.3390/molecules27103088.

Pełny tekst źródła
Streszczenie:
As one of the abundant and inexpensive metals on the earth, copper has demonstrated broad applications in synthetic chemistry and catalysis. Among these copper-catalyzed advances, copper carbenes are versatile and reactive intermediates that can mediate a variety of transformations, which have attracted much attention in the past decades. The present review summarizes two different reaction models that take place between a copper carbene intermediate and alkyne species, including the cross-coupling reaction of copper carbene intermediate with terminal alkyne, and the addition of copper carbene intermediate onto the C–C triple bond. This article will cover the profile from 2010 to 2021 by placing emphasis on the detailed catalytic models and highlighting the synthetic applications offered by these practical and mild methods.
Style APA, Harvard, Vancouver, ISO itp.
35

Liew, Sean K., Aleksandra Holownia, Diego B. Diaz, Philip A. Cistrone, Philip E. Dawson i Andrei K. Yudin. "Borylated oximes: versatile building blocks for organic synthesis". Chem. Commun. 53, nr 81 (2017): 11237–40. http://dx.doi.org/10.1039/c7cc06579e.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
36

Berger, Olivier, i Jean-Luc Montchamp. "General synthesis of P-stereogenic compounds: the menthyl phosphinate approach". Organic & Biomolecular Chemistry 14, nr 31 (2016): 7552–62. http://dx.doi.org/10.1039/c6ob01413e.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
37

Bayer, Patrick, Josef Schachtner, Michal Májek i Axel Jacobi von Wangelin. "Visible light-mediated photo-oxygenation of arylcyclohexenes". Organic Chemistry Frontiers 6, nr 16 (2019): 2877–83. http://dx.doi.org/10.1039/c9qo00493a.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
38

Santamaría, Javier, i Enrique Aguilar. "Beyond Fischer and Schrock carbenes: non-heteroatom-stabilized group 6 metal carbene complexes – a general overview". Organic Chemistry Frontiers 3, nr 11 (2016): 1561–88. http://dx.doi.org/10.1039/c6qo00206d.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
39

Hearne, Zoë, i Chao-Jun Li. "Palladium-catalysed atom-economical synthesis of conjugated dienals from terminal acetylenes and acrolein". Chemical Communications 53, nr 45 (2017): 6136–39. http://dx.doi.org/10.1039/c7cc02767b.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
40

Iftikhar, Ramsha, Aqsa Mazhar, Muhammad Saqlain Iqbal, Faiza Zahid Khan, Syed Hassan Askary i Hifza Sibtain. "Ring forming transformations of ynamides via cycloaddition". RSC Advances 13, nr 16 (2023): 10715–56. http://dx.doi.org/10.1039/d3ra00139c.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
41

Turrini, Nikolaus G., Răzvan C. Cioc, Daan J. H. van der Niet, Eelco Ruijter, Romano V. A. Orru, Mélanie Hall i Kurt Faber. "Biocatalytic access to nonracemic γ-oxo esters via stereoselective reduction using ene-reductases". Green Chemistry 19, nr 2 (2017): 511–18. http://dx.doi.org/10.1039/c6gc02493a.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
42

Prasad, Sure Siva, Dirgha Raj Joshi, Jeong Hwa Lee i Ikyon Kim. "One-pot access to 2-amino-3-arylbenzofurans: direct entry to polyheterocyclic chemical space". Organic & Biomolecular Chemistry 18, nr 40 (2020): 8119–40. http://dx.doi.org/10.1039/d0ob01715a.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
43

Lynch, Dylan M., i Eoin M. Scanlan. "Thiyl Radicals: Versatile Reactive Intermediates for Cyclization of Unsaturated Substrates". Molecules 25, nr 13 (7.07.2020): 3094. http://dx.doi.org/10.3390/molecules25133094.

Pełny tekst źródła
Streszczenie:
Sulfur centered radicals are widely employed in chemical synthesis, in particular for alkene and alkyne hydrothiolation towards thioether bioconjugates. The steadfast radical chain process that enables efficient hydrothiolation has been explored in the context of cascade reactions to furnish complex molecular architectures. The use of thiyl radicals offers a much cheaper and less toxic alternative to the archetypal organotin-based radical methods. This review outlines the development of thiyl radicals as reactive intermediates for initiating carbocyclization cascades. Key developments in cascade cyclization methodology are presented and applications for natural product synthesis are discussed. The review provides a chronological account of the field, beginning in the early seventies up to very recent examples; a span of almost 50 years.
Style APA, Harvard, Vancouver, ISO itp.
44

X. Xiang, Alan, Ricardo Lira, Konstantinos A. Agrios, Thomas Doundoulakis, Klaus B. Simonsen i Stephen E. Webber. "An Efficient Synthesis of (±)-Myxopyronin B via Versatile Pyridone Intermediates". HETEROCYCLES 68, nr 6 (2006): 1099. http://dx.doi.org/10.3987/com-06-10733.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
45

Barcelo, Gérard, Jean-Pierre Senet i Gérard Sennyey. "1,2,2,2-Tetrachloroethyl Carbamates: Versatile Intermediates for the Synthesis ofN-Nitrosoureas". Synthesis 1987, nr 11 (1987): 1027–29. http://dx.doi.org/10.1055/s-1987-28160.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
46

Dondoni, Alessandro, i Alberto Marra. "Thiazolylketoses: a new class of versatile intermediates for glycoside synthesis". Chemical Communications, nr 21 (1999): 2133–45. http://dx.doi.org/10.1039/a903758f.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
47

Maduli, Elvis J. M., Steven J. Edeson, Stephen Swanson, Panayiotis A. Procopiou i Joseph P. A. Harrity. "2-Iodoisatogens: Versatile Intermediates for the Synthesis of Nitrogen Heterocycles". Organic Letters 17, nr 2 (23.12.2014): 390–92. http://dx.doi.org/10.1021/ol503487f.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
48

Kataja, Antti O., i Géraldine Masson. "Imine and iminium precursors as versatile intermediates in enantioselective organocatalysis". Tetrahedron 70, nr 46 (listopad 2014): 8783–815. http://dx.doi.org/10.1016/j.tet.2014.06.101.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
49

Wu, Chien-Hsin, Li-Yun Chen, Ru-Jong Jeng i Shenghong A. Dai. "100% Atom-Economy Efficiency of Recycling Polycarbonate into Versatile Intermediates". ACS Sustainable Chemistry & Engineering 6, nr 7 (28.05.2018): 8964–75. http://dx.doi.org/10.1021/acssuschemeng.8b01326.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
50

Martin, Stephen F., i Michael P. Dwyer. "Iodocyclopropanes as versatile intermediates for the synthesis of substituted cyclopropanes". Tetrahedron Letters 39, nr 12 (marzec 1998): 1521–24. http://dx.doi.org/10.1016/s0040-4039(98)00072-0.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
Oferujemy zniżki na wszystkie plany premium dla autorów, których prace zostały uwzględnione w tematycznych zestawieniach literatury. Skontaktuj się z nami, aby uzyskać unikalny kod promocyjny!

Do bibliografii