Thematische Bibliographien / Allylamides / Zeitschriftenartikel
Um die anderen Arten von Veröffentlichungen zu diesem Thema anzuzeigen, folgen Sie diesem Link: Allylamides.

Zeitschriftenartikel zum Thema „Allylamides“

Autor: Grafiati
Veröffentlicht am 23. November 2024

Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an

Wählen Sie eine Art der Quelle aus:

Machen Sie sich mit Top-50 Zeitschriftenartikel für die Forschung zum Thema "Allylamides" bekannt.

Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.

Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.

Sehen Sie die Zeitschriftenartikel für verschiedene Spezialgebieten durch und erstellen Sie Ihre Bibliographie auf korrekte Weise.

1

Krompiec, Stanisław, Mariola Pigulla, Michał Krompiec, Stefan Baj, Julita Mrowiec-Białoń und Janusz Kasperczyk. „Highly selective isomerization of N-allylamides and N-allylamines“. Tetrahedron Letters 45, Nr. 27 (Juni 2004): 5257–61. http://dx.doi.org/10.1016/j.tetlet.2004.05.023.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
2

Chiacchio, Ugo, Gianluigi Broggini, Roberto Romeo, Silvia Gazzola, Maria A. Chiacchio, Salvatore V. Giofrè, Bartolo Gabriele, Raffaella Mancuso, Giuseppe Floresta und Chiara Zagni. „Intramolecular oxidative palladium-catalyzed diamination reactions of alkenyl sulfamates: an efficient synthesis of [1,2,5]thiadiazolo-fused piperazinones“. RSC Advances 6, Nr. 62 (2016): 57521–29. http://dx.doi.org/10.1039/c6ra13141g.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
3

Ranjith, Jala, Nomula Rajesh, Balasubramanian Sridhar und Palakodety Radha Krishna. „Intramolecular oxyacetoxylation of N-allylamides: an expeditious synthesis of oxazolines and oxazines by using a PhI(OAc)2/hydrogen fluoride–pyridine system“. Organic & Biomolecular Chemistry 14, Nr. 42 (2016): 10074–79. http://dx.doi.org/10.1039/c6ob01752e.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
4

Deng, Qiao-Hui, Jia-Rong Chen, Qiang Wei, Quan-Qing Zhao, Liang-Qiu Lu und Wen-Jing Xiao. „Visible-light-induced photocatalytic oxytrifluoromethylation of N-allylamides for the synthesis of CF3-containing oxazolines and benzoxazines“. Chem. Commun. 51, Nr. 17 (2015): 3537–40. http://dx.doi.org/10.1039/c4cc10217g.

Der volle Inhalt der Quelle
Annotation:
A visible-light-induced photocatalytic oxytrifluoro-methylation reaction of N-allylamides has been described for the efficient synthesis of CF3-containing oxazolines and benzoxazines in generally high yields.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
5

Chen, Zhichao, Hong Zhang, Shu-Feng Zhou und Xiuling Cui. „Photoredox-catalyzed synthesis of sulfonated oxazolines from N-allylamides through the insertion of sulfur dioxide“. Organic Chemistry Frontiers 9, Nr. 2 (2022): 364–69. http://dx.doi.org/10.1039/d1qo01540k.

Der volle Inhalt der Quelle
Annotation:
Photoredox-catalyzed generation of sulfonated oxazolines starting from N-allylamides, DABCO·(SO2)2, and aryldiazonium salts has been developed and a range of sulfonated oxazolines were obtained in moderate to good yields.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
6

Neugnot, Benjamin, Jean-Christophe Cintrat und Bernard Rousseau. „A new highly chemoselective isomerization of allylamides“. Tetrahedron 60, Nr. 16 (April 2004): 3575–79. http://dx.doi.org/10.1016/j.tet.2004.03.004.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
7

Krainova, G. F., I. A. Tolmacheva, M. N. Gorbunova und V. V. Grishko. „Synthesis of lupane and a-secolupane allylamides“. Chemistry of Natural Compounds 49, Nr. 2 (Mai 2013): 281–85. http://dx.doi.org/10.1007/s10600-013-0582-4.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
8

Wylie, Luke, Matthew Flynn, Victoria L. Blair, Philip C. Andrews und Ekaterina I. Izgorodina. „Isomers of Alkali Metal (Methylbenzyl)allylamides: A Theoretical Perspective“. ACS Omega 5, Nr. 16 (13.04.2020): 9448–57. http://dx.doi.org/10.1021/acsomega.0c00652.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
9

Moon, Nicholas G., und Andrew M. Harned. „Iodine(III)-promoted synthesis of oxazolines from N-allylamides“. Tetrahedron Letters 54, Nr. 23 (Juni 2013): 2960–63. http://dx.doi.org/10.1016/j.tetlet.2013.03.140.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
10

Chiusoli, Gian Paolo, Mirco Costa und Fausto Pivetti. „Rhodium-catalyzed coupling of N-allylamides of organic acids“. Journal of Organometallic Chemistry 373, Nr. 3 (September 1989): 385–89. http://dx.doi.org/10.1016/0022-328x(89)85067-3.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
11

Fu, Hua, Jipan Yu, Hua Tian, Chang Gao, Haijun Yang und Yuyang Jiang. „Boron-Catalyzed Arylthiooxygenation of N-Allylamides: Synthesis of (Arylsulfanyl)oxazolines“. Synlett 26, Nr. 05 (08.01.2015): 676–80. http://dx.doi.org/10.1055/s-0034-1378948.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
12

Ojima, Iwao, und Zhaoda Zhang. „Novel amide-directed hydrocarbonylations and double carbonylation of N-allylamides“. Journal of Organic Chemistry 53, Nr. 18 (September 1988): 4422–25. http://dx.doi.org/10.1021/jo00253a051.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
13

Gorbunova, M. N., G. F. Krainova, I. A. Tolmacheva und V. V. Grishko. „Synthesis of new biologically active polymer bioconjugates based on lupane allylamides“. Russian Journal of Bioorganic Chemistry 41, Nr. 7 (27.11.2015): 732–38. http://dx.doi.org/10.1134/s1068162015070043.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
14

Hesse, Manfred, und Sergey Sergeyev. „A New Convenient Method for the Preparation of Enamides fromN-Allylamides“. Synlett, Nr. 8 (2002): 1313–17. http://dx.doi.org/10.1055/s-2002-32962.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
15

Moon, Nicholas G., und Andrew M. Harned. „ChemInform Abstract: Iodine(III)-Promoted Synthesis of Oxazolines from N-Allylamides.“ ChemInform 44, Nr. 37 (22.08.2013): no. http://dx.doi.org/10.1002/chin.201337115.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
16

Halli, Juliette, Philipp Kramer, Maren Bechthold und Georg Manolikakes. „Nickel-Catalyzed Synthesis of Enamides and EnecarbamatesviaIsomerization of Allylamides and Allylcarbamates“. Advanced Synthesis & Catalysis 357, Nr. 14-15 (25.09.2015): 3321–24. http://dx.doi.org/10.1002/adsc.201500461.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
17

Krompiec, Stanisław, Mariola Pigulla, Nikodem Kuźnik, Michał Krompiec, Bogdan Marciniec, Dariusz Chadyniak und Janusz Kasperczyk. „Highly selective isomerization of N-allylamides catalyzed by ruthenium and rhodium complexes“. Journal of Molecular Catalysis A: Chemical 225, Nr. 1 (Januar 2005): 91–101. http://dx.doi.org/10.1016/j.molcata.2004.09.001.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
18

Mukhopadhyay, Manoj, und Javed Iqbal. „Co(III)DMG-Catalyzed Synthesis of Allylamides from Allyl Alcohols and Acetonitrile“. Journal of Organic Chemistry 62, Nr. 6 (März 1997): 1843–45. http://dx.doi.org/10.1021/jo960557q.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
19

Wang, Lu, Chao Liu, Ruopeng Bai, Yani Pan und Aiwen Lei. „Easy access to enamides: a mild nickel-catalysed alkene isomerization of allylamides“. Chemical Communications 49, Nr. 72 (2013): 7923. http://dx.doi.org/10.1039/c3cc43875a.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
20

Prati, Fabio, Alberto Spaggiari, Daniele Vaccari und Paolo Davoli. „The Triphenyl Phosphite-Chlorine Reagent in the Synthesis of Pyrroles fromN-Allylamides“. Synthesis, Nr. 6 (2006): 995–98. http://dx.doi.org/10.1055/s-2006-926365.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
21

Yu, Jipan, Hua Tian, Chang Gao, Haijun Yang, Yuyang Jiang und Hua Fu. „ChemInform Abstract: Boron-Catalyzed Arylthiooxygenation of N-Allylamides: Synthesis of (Arylsulfanyl)oxazolines.“ ChemInform 46, Nr. 30 (Juli 2015): no. http://dx.doi.org/10.1002/chin.201530179.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
22

Matsumoto, Kouichi, Jun-ichi Yoshida, Yu Miyamoto, Naoya Mitani, Rina Yanagi, Shigenori Kashimura und Seiji Suga. „Synthesis of Oxazolines from N-Allylamides Using an Electrochemically Generated ArS(ArSSAr)+ Pool“. HETEROCYCLES 96, Nr. 8 (2018): 1373. http://dx.doi.org/10.3987/com-18-13942.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
23

Yang, Chun-Hua, Zhong-Qi Xu, Lili Duan und Yue-Ming Li. „CuBr 2 -promoted intramolecular bromocyclization of N-allylamides and aryl allyl ketone oximes“. Tetrahedron 73, Nr. 48 (November 2017): 6747–53. http://dx.doi.org/10.1016/j.tet.2017.10.025.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
24

Walters, Michael A., Colleen S. McDonough, Perry S. Brown und Andrew B. Hoem. „An extremely mild 3-aza-Claisen reaction. 1. Rearrangement of simple N-allylamides.“ Tetrahedron Letters 32, Nr. 2 (Januar 1991): 179–82. http://dx.doi.org/10.1016/0040-4039(91)80848-z.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
25

Hilt, Gerhard, Felicia Weber, Philipp Steinlandt und Monika Ballmann. „Structure-Dependent Nickel-Catalysed Transposition of N-Allylamides to E- or Z-Enamides“. Synthesis 49, Nr. 02 (14.11.2016): 440–50. http://dx.doi.org/10.1055/s-0036-1588340.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
26

Hu, Yancheng, Xincheng Li und Boshun Wan. „NIS-mediated ring-closure/opening cascade reactions of allylamides: an expedient route to oxazolines“. Tetrahedron 71, Nr. 38 (September 2015): 6935–43. http://dx.doi.org/10.1016/j.tet.2015.07.011.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
27

Yu, Jipan, Haijun Yang und Hua Fu. „Transition Metal-Free Trifluoromethylation ofN-Allylamides with Sodium Trifluoromethanesulfinate: Synthesis of Trifluoromethyl-Containing Oxazolines“. Advanced Synthesis & Catalysis 356, Nr. 17 (05.11.2014): 3669–75. http://dx.doi.org/10.1002/adsc.201400144.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
28

Zhang, Xiaowei, Bonan Cao, Shichao Yu und Xumu Zhang. „Rhodium-Catalyzed Asymmetric Hydroformylation of N-Allylamides: Highly Enantioselective Approach to β2-Amino Aldehydes“. Angewandte Chemie International Edition 49, Nr. 24 (29.04.2010): 4047–50. http://dx.doi.org/10.1002/anie.201000955.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
29

Zhang, Xiaowei, Bonan Cao, Shichao Yu und Xumu Zhang. „Rhodium-Catalyzed Asymmetric Hydroformylation of N-Allylamides: Highly Enantioselective Approach to β2-Amino Aldehydes“. Angewandte Chemie 122, Nr. 24 (29.04.2010): 4141–44. http://dx.doi.org/10.1002/ange.201000955.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
30

MUKHOPADHYAY, M., und J. IQBAL. „ChemInform Abstract: Co(III)DMG-Catalyzed Synthesis of Allylamides from Allyl Alcohols and Acetonitrile.“ ChemInform 28, Nr. 30 (03.08.2010): no. http://dx.doi.org/10.1002/chin.199730070.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
31

Wang, Lu, Chao Liu, Ruopeng Bai, Yani Pan und Aiwen Lei. „ChemInform Abstract: Easy Access to Enamides: A Mild Nickel-Catalyzed Alkene Isomerization of Allylamides.“ ChemInform 45, Nr. 2 (19.12.2013): no. http://dx.doi.org/10.1002/chin.201402073.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
32

Sergeyev, Sergey, und Manfred Hesse. „ChemInform Abstract: A New Convenient Method for the Preparation of Enamides from N-Allylamides.“ ChemInform 33, Nr. 45 (19.05.2010): no. http://dx.doi.org/10.1002/chin.200245083.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
33

Ghannoum, Mahmoud. „Azole Resistance in Dermatophytes“. Journal of the American Podiatric Medical Association 106, Nr. 1 (01.01.2016): 79–86. http://dx.doi.org/10.7547/14-109.

Der volle Inhalt der Quelle
Annotation:
Azole antifungal agents (eg, fluconazole and itraconazole) have been widely used to treat superficial fungal infections caused by dermatophytes and, unlike the allylamines (such as terbinafine and naftifine), have been associated with resistance development. Although many published manuscripts describe resistance to azoles among yeast and molds, reports describing resistance of dermatophytes are starting to appear. In this review, I discuss the mode of action of azole antifungals and mechanisms underlying their resistance compared with the allylamine class of compounds. Data from published and original studies were compared and summarized, and their clinical implications are discussed. In contrast to the cidal allylamines, static drugs such as azoles permit the occurrence of mutations in enzymes involved in ergosterol biosynthesis, and the ergosterol precursors accumulating as a consequence of azole action are not toxic. Azole antifungals, unlike allylamines, potentiate resistance development in dermatophytes.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
34

Bezemer, Jacob M., Jacob van der Ende, Jacqueline Limpens, Henry J. C. de Vries und Henk D. F. H. Schallig. „Safety and efficacy of allylamines in the treatment of cutaneous and mucocutaneous leishmaniasis: A systematic review“. PLOS ONE 16, Nr. 4 (07.04.2021): e0249628. http://dx.doi.org/10.1371/journal.pone.0249628.

Der volle Inhalt der Quelle
Annotation:
Cutaneous and mucocutaneous leishmaniasis affect a million people yearly, leading to skin lesions and potentially disfiguring mucosal disease. Current treatments can have severe side effects. Allylamine drugs, like terbinafine, are safe, including during pregnancy. This review assesses efficacy and safety of allylamines for the treatment of cutaneous and mucocutaneous leishmaniasis. It followed the PRISMA statement for reporting and was preregistered in PROSPERO(CRD4201809068). MEDLINE, EMBASE, the Cochrane Central Register of Controlled Trials, the Global Health Library, Web of Science, Google Scholar, and clinical trial registers were searched from their creation to May 24th, 2020. All original human, animal, and in vitro studies concerning allylamines and cutaneous or mucocutaneous leishmaniasis were eligible for inclusion. Comparators—if any—included both placebo or alternative cutaneous or mucocutaneous leishmaniasis treatments. Complete cure, growth inhibition, or adverse events served as outcomes. The search identified 312 publications, of which 22 were included in this systematic review. There were one uncontrolled and two randomised controlled trials. The only well-designed randomised controlled trial that compared the treatment efficacy of oral terbinafine versus intramuscular meglumine antimoniate in 80 Leismania tropica infected patients showed a non-significant lower cure rate for terbinafine vs meglumine antimoniate (38% vs 53%). A meta-analysis could not be performed due to the small number of studies, their heterogeneity, and low quality. This systematic review shows that there is no evidence of efficacy of allylamine monotherapy against cutaneous and mucocutaneous leishmaniasis. Further trials of allylamines should be carefully considered as the outcomes of an adequately designed trial were disappointing and in vitro studies indicate minimal effective concentrations that are not achieved in the skin during standard doses. However, the in vitro synergistic effects of allylamines combined with triazole drugs warrant further exploration.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
35

Chiba, Shunsuke, Line Zhang, Jian-Yuan Lee und Naomi Yamazaki. „Copper(II)-Catalyzed Synthesis of Pyrazinones from α-Azido-N-allylamides under an Oxygen Atmosphere“. Synlett 2011, Nr. 15 (12.08.2011): 2167–70. http://dx.doi.org/10.1055/s-0030-1261185.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
36

Halli, Juliette, Philipp Kramer, Maren Bechthold und Georg Manolikakes. „ChemInform Abstract: Nickel-Catalyzed Synthesis of Enamides and Enecarbamates via Isomerization of Allylamides and Allylcarbamates.“ ChemInform 47, Nr. 9 (Februar 2016): no. http://dx.doi.org/10.1002/chin.201609020.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
37

Klychnikov, Mikhail K., Radek Pohl, Ivana Císařová und Ullrich Jahn. „α,γ-Dioxygenated amides via tandem Brook rearrangement/radical oxygenation reactions and their application to syntheses of γ-lactams“. Beilstein Journal of Organic Chemistry 17 (09.03.2021): 688–704. http://dx.doi.org/10.3762/bjoc.17.58.

Der volle Inhalt der Quelle
Annotation:
Pyrrolidones are common heterocyclic fragments in various biologically active compounds. Here, a two-step radical-based approach to γ-lactams bearing three to four stereocenters starting from epoxides, N-allylic silylacetamides and TEMPO is reported. The sequence starts with a new tandem nucleophilic substitution/Brook rearrangement/single electron transfer-induced radical oxygenation furnishing orthogonally protected α,γ-dioxygenated N-allylamides with wide scope, mostly good yields, and partly good diastereo- and enantioselectivity for defined combinations of chiral epoxides and chiral amides. This represents a very rare example of an oxidative geminal C–C/C–O difunctionalization next to carbonyl groups. The resulting dioxygenated allylic amides are subsequently subjected to persistent radical effect-based 5-exo-trig radical cyclization reactions providing functionalized pyrrolidones in high yields as diastereomeric mixtures. They converge to 3,4-trans-γ-lactams by base-mediated equilibration, which can be easily further diversified. Stereochemical models for both reaction types were developed.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
38

Ueda, Kazutaka, und Miwako Mori. „Synthesis of allylamides from allyl halides, carbon monoxide, and titanium–nitrogen complexes prepared from molecular nitrogen“. Tetrahedron Letters 45, Nr. 14 (März 2004): 2907–10. http://dx.doi.org/10.1016/j.tetlet.2004.02.072.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
39

Zhang, Xiaowei, Bonan Cao, Shichao Yu und Xumu Zhang. „ChemInform Abstract: Rhodium-Catalyzed Asymmetric Hydroformylation of N-Allylamides: Highly Enantioselective Approach to β2-Amino Aldehydes.“ ChemInform 41, Nr. 38 (26.08.2010): no. http://dx.doi.org/10.1002/chin.201038044.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
40

Broggini, Gianluigi, Egle M. Beccalli, Tea Borelli, Filippo Brusa, Silvia Gazzola und Alberto Mazza. „Intra-Intermolecular Palladium-Catalyzed Domino Reactions of Glycine Allylamides for the Synthesis of Diversely Functionalized Piperazinones“. European Journal of Organic Chemistry 2015, Nr. 19 (27.05.2015): 4261–68. http://dx.doi.org/10.1002/ejoc.201500386.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
41

Akssira, Mohamed, Farid El Guemmout, Patrick Bauchat und André Foucaud. „Synthèses de diallylamines et triallylamines à partir des 3-acetoxy-3-aryl-2-méthylène propionitriles et des 3-acétoxy-3-aryl-2-méthylène propionates de méthyle“. Canadian Journal of Chemistry 72, Nr. 5 (01.05.1994): 1357–61. http://dx.doi.org/10.1139/v94-169.

Der volle Inhalt der Quelle
Annotation:
The reactions of 3-acetoxy-3-aryl-2-methylene propionitriles 1 with ammonia yielded the corresponding diallylamines 3ZZ. The reaction of 1 with a primary allylamine or with ethylene diamine gave the diallylamine 11 or 13ZZ. The treatment of methyl 3-acetoxy-3-aryl-2-methylene propionates 2 with isopropylamine or ethylene diamine gave the allylamines 6EE or 14 and 15, but the reaction of 2 with ammonia gave only the triallylamines 4EEE in good yields.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
42

Li, Yali, Lingjuan Zhang, Zongyao Zhang, Jianbin Xu, Yixiao Pan, Conghui Xu, Lingxian Liu et al. „Regio- and Stereoselective Synthesis of 1,2,3-Trisubstituted Indanes from Diarylmethanols and Allylamides through Iron(III) Chloride Hexahydrate“. Advanced Synthesis & Catalysis 358, Nr. 13 (16.06.2016): 2148–55. http://dx.doi.org/10.1002/adsc.201600165.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
43

Zhang, Line, Jian-Yuan Lee, Naomi Yamazaki und Shunsuke Chiba. „ChemInform Abstract: Copper(II)-Catalyzed Synthesis of Pyrazinones from α-Azido-N-allylamides under an Oxygen Atmosphere.“ ChemInform 43, Nr. 5 (05.01.2012): no. http://dx.doi.org/10.1002/chin.201205199.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
44

Yu, Jipan, Haijun Yang und Hua Fu. „ChemInform Abstract: Transition Metal-Free Trifluoromethylation of N-Allylamides with Sodium Trifluoromethanesulfinate: Synthesis of Trifluoromethyl-Containing Oxazolines.“ ChemInform 46, Nr. 18 (16.04.2015): no. http://dx.doi.org/10.1002/chin.201518154.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
45

Broggini, Gianluigi, Egle M. Beccalli, Tea Borelli, Filippo Brusa, Silvia Gazzola und Alberto Mazza. „ChemInform Abstract: Intra-Intermolecular Palladium-Catalyzed Domino Reactions of Glycine Allylamides for the Synthesis of Diversely Functionalized Piperazinones.“ ChemInform 46, Nr. 45 (22.10.2015): no. http://dx.doi.org/10.1002/chin.201545184.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
46

Deng, Qiao-Hui, Jia-Rong Chen, Qiang Wei, Quan-Qing Zhao, Liang-Qiu Lu und Wen-Jing Xiao. „ChemInform Abstract: Visible-Light-Induced Photocatalytic Oxytrifluoromethylation of N-Allylamides for the Synthesis of CF3-Containing Oxazolines and Benzoxazines.“ ChemInform 46, Nr. 28 (25.06.2015): no. http://dx.doi.org/10.1002/chin.201528171.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
47

Kawamura, Shintaro, Daisuke Sekine und Mikiko Sodeoka. „Synthesis of CF3-containing oxazolines via trifluoromethylation of allylamides with Togni reagent in the presence of alkali metal iodides“. Journal of Fluorine Chemistry 203 (November 2017): 115–21. http://dx.doi.org/10.1016/j.jfluchem.2017.07.012.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
48

Thiedemann, Birk, Christin M. L. Schmitz und Anne Staubitz. „Reduction of N-Allylamides by LiAlH4: Unexpected Attack of the Double Bond with Mechanistic Studies of Product and Byproduct Formation“. Journal of Organic Chemistry 79, Nr. 21 (27.10.2014): 10284–95. http://dx.doi.org/10.1021/jo501907v.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
49

Broggini, Gianluigi, Vincenzina Barbera, Egle M. Beccalli, Elena Borsini, Simona Galli, Giuseppe Lanza und Gaetano Zecchi. „Palladium(II)/Copper Halide/Solvent Combination for Selective Intramolecular Domino Reactions of Indolecarboxylic Acid Allylamides: An Unprecedented Arylation/Esterification Sequence“. Advanced Synthesis & Catalysis 354, Nr. 1 (Januar 2012): 159–70. http://dx.doi.org/10.1002/adsc.201100614.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
50

Li, Yutian, Li Wang, Shengbin Zhou, Guoxue He und Yu Zhou. „Electrochemical oxidative cyclization of N-allylamides for the synthesis of CF3-containing benzoxazines and oxazolines“. RSC Advances 14, Nr. 1 (2024): 154–59. http://dx.doi.org/10.1039/d3ra07282g.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
Die Auswahlen zum Thema "Allylamides" für andere Quellenarten können Sie auch interessieren:
Dissertationen
Wir bieten Rabatte auf alle Premium-Pläne für Autoren, deren Werke in thematische Literatursammlungen aufgenommen wurden. Kontaktieren Sie uns, um einen einzigartigen Promo-Code zu erhalten!

Zur Bibliographie