Regioselective Reactions of Pyridine-2-sulfenyl Bromide with Vinyl and Allyl Ethers.
- Published in:
- Russian Journal of General Chemistry, 2022, v. 92, n. 9, p. 1720, doi. 10.1134/S1070363222090146
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- Article
Works matching DE "VINYL bromide"
Results: 31
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Vinyl Esters and Vinyl Sulfonates as Green Alternatives to Vinyl Bromide for the Synthesis of Monosubstituted Alkenes via Transition-Metal-Catalyzed Reactions.
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- Chemistry (2624-8549), 2023, v. 5, n. 4, p. 2288, doi. 10.3390/chemistry5040153
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- Article
3
Sequential Vinyl Radical Cyclization/Fixation of Carbon Dioxide through Electrochemical Reduction of Vinyl Bromide in the Presence of an Electron-Transfer Mediator.
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- ChemElectroChem, 2016, v. 3, n. 12, p. 2052, doi. 10.1002/celc.201600508
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- Article
4
Reactions of 2,3-Dibromo-2-methylpropanamides Promoted by Potassium tert-Butoxide.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 10, p. 1643, doi. 10.1134/S1070428021100122
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- Article
5
Impact of Thermo-Physical Data on the Modeling of High-Pressure Polymerizations.
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- Chemie Ingenieur Technik (CIT), 2016, v. 88, n. 11, p. 1665, doi. 10.1002/cite.201600082
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- Article
6
Efficient Stille cross-coupling reaction catalysed by the Pd(OAc)<sub>2</sub>/orotic acid catalytic system.
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- Journal of Chemical Research, 2013, v. 37, n. 4, p. 219, doi. 10.3184/174751913X13635315066265
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- Article
7
Jatrophane Diterpenes: Preparation of the Western Fragment of Pl-3.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 5, p. 919, doi. 10.1002/ejoc.201301616
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- Article
8
Synthese α‐chiraler Ketone und chiraler Alkane durch eine radikalisch/ionische Kreuzungsreaktion von Vinyl‐Bor‐At‐Komplexen.
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- Angewandte Chemie, 2018, v. 130, n. 9, p. 2466, doi. 10.1002/ange.201711390
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- Article
9
Enantiospecific Alkynylation of Alkylboronic Esters.
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- Angewandte Chemie, 2016, v. 128, n. 13, p. 4342, doi. 10.1002/ange.201600599
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- Article
10
Bimetallic Pd/Cu‐Catalyzed Sonogashira Coupling‐Elimination Reaction: An Efficient Synthesis of 2‐Unsubstituted Terminal 1, 3‐Enynes.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 6, p. 1, doi. 10.1002/ajoc.202300129
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- Article
11
Decarboxylative Perfluoroalkylation of Vinyl Bromides with Copper(I) Perfluorocarboxylato Complexes.
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- Asian Journal of Organic Chemistry, 2016, v. 5, n. 11, p. 1406, doi. 10.1002/ajoc.201600348
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- Article
12
Visible-Light-Promoted Nickel- and Organic-Dye-Cocatalyzed Formylation Reaction of Aryl Halides and Triflates and Vinyl Bromides with Diethoxyacetic Acid as a Formyl Equivalent.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 6, p. 1500, doi. 10.1002/anie.201610108
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- Article
13
Preparation of Vinyl Arenes by Nickel-Catalyzed Reductive Coupling of Aryl Halides with Vinyl Bromides.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 50, p. 15544, doi. 10.1002/anie.201607959
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- Article
14
Palladium(0)-Catalyzed Cross-Coupling of 1,1-Diboronates with Vinyl Bromides and 1,1-Dibromoalkenes.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 44, p. 11921, doi. 10.1002/anie.201407000
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- Article
15
FTIR and Raman Spectroscopy Study of Soot Deposits Produced in the Infrared Multiphoton Dissociation of Vinyl Bromide.
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- Journal of Spectroscopy, 2022, p. 1, doi. 10.1155/2022/9942870
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- Article
16
An Alternative Route to Complex Allenes or Cyclooctatrienes via a Suzuki Cyclocarbopalladation Cascade.
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- Chemistry - A European Journal, 2022, v. 28, n. 4, p. 1, doi. 10.1002/chem.202103502
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- Article
17
Dichromatic irradiation studies of C2a3Πu radical formation with TEA CO<sub>2</sub> laser heating of C<sub>2</sub>H<sub>3</sub>Br/CF<sub>2</sub>HCl mixtures.
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- Optical & Quantum Electronics, 2024, v. 56, n. 6, p. 1, doi. 10.1007/s11082-024-06847-0
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- Article
18
Hexa- peri-hexabenzocoronene with Different Acceptor Units for Tuning Optoelectronic Properties.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 19, p. 2710, doi. 10.1002/asia.201600638
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- Article
19
Palladium‐Catalyzed C−H Alkenylation of α‐Aryl Alkyl Nitriles.
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- ChemCatChem, 2024, v. 16, n. 13, p. 1, doi. 10.1002/cctc.202301730
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- Article
20
Nickel‐Catalyzed Electrosynthesis of Aryl and Vinyl Phosphinates.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 23, p. 3452, doi. 10.1002/ejoc.202000422
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- Article
21
Heck Reactions of Acrolein or Enones and Aryl Bromides – Synthesis of 3‐Aryl Propenals or Propenones and Consecutive Application in Multicomponent Pyrazole Syntheses.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 14, p. 2086, doi. 10.1002/ejoc.202000066
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- Article
22
2,2‐Difluorovinyl Pinacolborane – A New Versatile Reagent for the Suzuki–Miyaura Reaction.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 37, p. 6417, doi. 10.1002/ejoc.201901118
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- Article
23
N-Vinylation of Imidazole and Benzimidazole with a Paramagnetic Vinyl Bromide.
- Published in:
- Molbank, 2018, v. 2018, n. 1, p. m980, doi. 10.3390/M980
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24
O<sub>2</sub>‐Assisted Four‐Component Reaction of Vinyl Magnesium Bromide with Chiral N‐tert‐Butanesulfinyl Imines To Form syn‐1,3‐Amino Alcohols.
- Published in:
- Angewandte Chemie, 2021, v. 133, n. 46, p. 24849, doi. 10.1002/ange.202109566
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- Article
25
Enantioselective Total Syntheses of Manginoids A and C and Guignardones A and C.
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- Angewandte Chemie, 2021, v. 133, n. 28, p. 15414, doi. 10.1002/ange.202104182
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- Article
26
Synthesis of Spiroindenyl-2-Oxindoles through Palladium-Catalyzed Spirocyclization of 2-Bromoarylamides and Vinyl Bromides.
- Published in:
- Molecules, 2021, v. 26, n. 24, p. 7496, doi. 10.3390/molecules26247496
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- Article
27
Thiazoles: A Retrospective Study on Synthesis, Structure-activity Relationship and Therapeutic Significance.
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- Indian Journal of Pharmaceutical Education & Research, 2022, v. 56, n. 3, p. 646, doi. 10.5530/ijper.56.3.113
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28
Pd‐Catalyzed Negishi Cross‐Coupling of Vinyl Bromides with Diborylmethylzinc Chloride.
- Published in:
- Bulletin of the Korean Chemical Society, 2021, v. 42, n. 3, p. 499, doi. 10.1002/bkcs.12212
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29
Palladium-catalyzed Intramolecular Coupling Reactions between Vinyl Bromides, Aryl and Vinyl Halides, and Aryl Iodides Mediated by Indium: Preparation of Five- to Eight-membered Carbocycles and Heterocycles.
- Published in:
- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 2, p. 711, doi. 10.1002/bkcs.10106
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30
Copper-Mediated Introduction of the CF<sub>2</sub>PO(OEt)<sub>2</sub> Motif: Scope and Limitations.
- Published in:
- Chemistry - A European Journal, 2017, v. 23, n. 68, p. 17318, doi. 10.1002/chem.201703542
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31
Chiral sulfide and achiral sulfonic acid cocatalyzed enantioselective electrophilic tandem selenylation semipinacol rearrangement of allenols.
- Published in:
- Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-57381-w
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- Article