Category: 1530-32-1

Li, Ping; Lee, Boon Chong; Zhang, Xiaoxiang; Koh, Ming Joo published an article in 2022. The article was titled 《Base-Mediated Site-Selective Hydroamination of Alkenes》, and you may find the article in Synthesis.Application In Synthesis of Ethyltriphenylphosphonium bromide The information in the text is summarized as follows:

A base-mediated hydroamination protocol, using substoichiometric amounts of a hydrosilane and potassium tert-butoxide, that operates under mild conditions at 30° is presented. Many aryl- and heteroatom-substituted olefins as well as arylamines are tolerated, affording the desired products with complete regioselectivity. Preliminary mechanistic investigations reveal a non-radical pathway for hydroamination. A sequential remote hydroamination strategy involving an initial Fe-catalyzed olefin isomerization followed by the base-mediated hydroamination was also developed to directly access β-arylamines from terminal aliphatic alkenes. In addition to this study using Ethyltriphenylphosphonium bromide, there are many other studies that have used Ethyltriphenylphosphonium bromide(cas: 1530-32-1Application In Synthesis of Ethyltriphenylphosphonium bromide) was used in this study.

Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. It is also used as catalysts in the synthesis of certain organic compounds and as a pharmaceutical intermediate.Application In Synthesis of Ethyltriphenylphosphonium bromide

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

《An effective synthesis of ursodeoxycholic acid from dehydroepiandrosterone》 was written by Chen, Wang; Hu, Daihua; Feng, Zili; Liu, Zhaopeng. HPLC of Formula: 1530-32-1This research focused onursodeoxycholic acid preparation Mitsunobu inversion Luche regioselective allyl oxidation; Dehydroepiandrosterone; Synthesis; Ursodeoxycholic acid. The article conveys some information:

A novel synthetic route of producing ursodeoxycholic acid (UDCA, I) was developed through multiple reactions from plant-source dehydroepiandrosterone (DHEA), with a Mitsunobu reaction and regioselective allyl oxidationat as the key steps. The reaction conditions of the key allyl oxidation reaction were also investigated and optimized, including solvent, oxidant and reaction temperature In this novel route for the preparation of UDCA, most of the reaction steps have high conversions and overall yield up to 35% for 8 steps. Since all starting materials are cost-effective, com. available and effectively avoided the risk of animal derived raw materials, this promising synthetic route offers economical and efficient strategies for potential production of UDCA. In the experimental materials used by the author, we found Ethyltriphenylphosphonium bromide(cas: 1530-32-1HPLC of Formula: 1530-32-1)

Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. CatOnium ETPB is also used as catalysts in the synthesis of certain organic compounds.HPLC of Formula: 1530-32-1

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Melin, Lea; Abdullayev, Shuay; Fnaiche, Ahmed; Vu, Victoria; Gonzalez Suarez, Narjara; Zeng, Hong; Szewczyk, Magdalena M.; Li, Fengling; Senisterra, Guillermo; Allali-Hassani, Abdellah; Chau, Irene; Dong, Aiping; Woo, Simon; Annabi, Borhane; Halabelian, Levon; LaPlante, Steven R.; Vedadi, Masoud; Barsyte-Lovejoy, Dalia; Santhakumar, Vijayaratnam; Gagnon, Alexandre published their research in ChemMedChem in 2021. The article was titled 《Development of LM98, a Small-Molecule TEAD Inhibitor Derived from Flufenamic Acid》.HPLC of Formula: 1530-32-1 The article contains the following contents:

The YAP-TEAD transcriptional complex is responsible for the expression of genes that regulate cancer cell growth and proliferation. Dysregulation of the Hippo pathway due to overexpression of TEAD has been reported in a wide range of cancers. Inhibition of TEAD represses the expression of associated genes, demonstrating the value of this transcription factor for the development of novel anti-cancer therapies. We report herein the design, synthesis and biol. evaluation of LM98, a flufenamic acid analog. LM98 shows strong affinity to TEAD, inhibits its autopalmitoylation and reduces the YAP-TEAD transcriptional activity. Binding of LM98 to TEAD was supported by 19F-NMR studies while co-crystallization experiments confirmed that LM98 is anchored within the palmitic acid pocket of TEAD. LM98 reduces the expression of CTGF and Cyr61, inhibits MDA-MB-231 breast cancer cell migration and arrests cell cycling in the S phase during cell division. In the experiment, the researchers used many compounds, for example, Ethyltriphenylphosphonium bromide(cas: 1530-32-1HPLC of Formula: 1530-32-1)

Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. It is also used as catalysts in the synthesis of certain organic compounds and as a pharmaceutical intermediate.HPLC of Formula: 1530-32-1

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

In 2022,Hu, Liqun; Liu, Yibing; Fang, Xiong; zheng, Yuzhu; Liao, Rong-zhen; Li, Man; Xie, Youwei published an article in ACS Catalysis. The title of the article was 《An Intermolecular Hydroarylation of Highly Deactivated Styrenes Catalyzed by Re2O7/HReO4 in Hexafluoroisopropanol》.Safety of Ethyltriphenylphosphonium bromide The author mentioned the following in the article:

Here, authors describe an activation mode for unactivated alkenes on the basis of a synergy between Re2O7/HReO4 and hexafluoroisopropanol (HFIP). Highly electron-deficient styrenes have been activated to effect a challenging intermol. hydroarylation with different arenes to give a variety of diarylalkanes in high efficiency. This method is characterized by mild reaction condition, broad substrate scope, high chem. yields, and minimal waste generation. The potential synthetic application of this methodol. was exemplified by the efficient synthesis of a retinoic acid receptor (RAR) agonist. DFT calculations and deuterium-labeling experiments were conducted to elucidate the reaction mechanism, and both confirmed the critical role of HFIP, which significantly reduced the energetical barriers for several key steps of this transformation via a network of hydrogen bonding to perrhenate anion with two equivalent of HFIP. In addition to this study using Ethyltriphenylphosphonium bromide, there are many other studies that have used Ethyltriphenylphosphonium bromide(cas: 1530-32-1Safety of Ethyltriphenylphosphonium bromide) was used in this study.

Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. It is also used as catalysts in the synthesis of certain organic compounds and as a pharmaceutical intermediate.Safety of Ethyltriphenylphosphonium bromide

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Wood, Devin P.; Guan, Weiyang; Lin, Song published their research in Synthesis in 2021. The article was titled 《Titanium and Cobalt Bimetallic Radical Redox Relay for the Isomerization of N-Bz Aziridines to Allylic Amides》.Computed Properties of C20H20BrP The article contains the following contents:

Herein, a bimetallic radical redox-relay strategy is employed to generate alkyl radicals under mild conditions with titanium(III) catalysis and terminated via hydrogen atom transfer with cobalt(II) catalysis to enact base-free isomerizations of N-Bz aziridines I [R1R3 = (CH2)3, R2 = H; R1R2 = CH2NTsCH2CH2, R3 = H; R1 = MeO2C(CH2)7, R2 = R3 = H; etc] to N-Bz allylic amides II. This reaction provides an alternative strategy for the synthesis of allylic amides from alkenes via a three-step sequence to accomplish a formal transpositional allylic amination. The experimental part of the paper was very detailed, including the reaction process of Ethyltriphenylphosphonium bromide(cas: 1530-32-1Computed Properties of C20H20BrP)

Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. It is also used as catalysts in the synthesis of certain organic compounds and as a pharmaceutical intermediate.Computed Properties of C20H20BrP

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Ning, Shulin; Zheng, Lianyou; Bai, Ya; Wang, Shutao; Wang, Siyu; Shi, Lingling; Gao, Qiansong; Che, Xin; Zhang, Zhuoqi; Xiang, Jinbao published their research in Tetrahedron in 2021. The article was titled 《Highly selective electroreductive linear dimerization of electron-deficient vinylarenes》.Application of 1530-32-1 The article contains the following contents:

A direct electroreductive dimerization of electron-deficient vinylarenes R1R2C:CR3R4 (R1 = Ph, 4-NCC6H4, pyridin-4-yl, etc., R2 = R3 = R4 = H; R1 = 4-EtO2CC6H4, R2 = Me, Ph, R3 = R4 = H; R1 = 4-MeO2CC6H4, R2 = H, R3 = Me, R4 = H, Me; etc.) for the synthesis of 1,4-diarylbutanes R1R2CH-CR3R4-CR3R4-CHR1R2 as been developed using a simple undivided cell with inexpensive carbon electrodes at room temperature The control and deuterium-labeling experiments of electroreductive dimerization suggest that the hydrogen source comes from the solvent CH3CN. This protocol provides a mild and efficient route for the construction of C-C bond in moderate to good yields with high regioselectivity and broad substrate scope. In the experiment, the researchers used Ethyltriphenylphosphonium bromide(cas: 1530-32-1Application of 1530-32-1)

Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. It is also used as catalysts in the synthesis of certain organic compounds and as a pharmaceutical intermediate.Application of 1530-32-1

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Forster, Dan; Guo, Weisi; Wang, Qian; Zhu, Jieping published their research in ACS Catalysis in 2021. The article was titled 《Photoredox Catalytic Three-Component Amidoazidation of 1,3-Dienes》.HPLC of Formula: 1530-32-1 The article contains the following contents:

Herein a three-component 1,2-amidoazidation of 1,3-dienes was reported. In the presence of fac-Ir(ppy)3 under blue LED irradiation, reaction of 1-aryl substituted 1,3-dienes with N-amidopyridinium salt and trimethylsilyl azide (TMSN3) affords exclusively the 1,2-amidoazidation products. The 1-alkyl substituted counterparts undergo the same reaction with moderate to high 1,2- vs 1,4-selectivity. Reduction of this mixture with PPh3 under dynamic kinetic conditions enriches significantly one of the two isomers thanks to the facile 1,3-azide shift (Winstein rearrangement) of the allyl azides. The results came from multiple reactions, including the reaction of Ethyltriphenylphosphonium bromide(cas: 1530-32-1HPLC of Formula: 1530-32-1)

Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. It is also used as catalysts in the synthesis of certain organic compounds and as a pharmaceutical intermediate.HPLC of Formula: 1530-32-1

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

In 2022,Yang, Biao; Dong, Kui; Li, Xiang-Sheng; Wu, Li-Zhu; Liu, Qiang published an article in Organic Letters. The title of the article was 《Photoacid-Enabled Synthesis of Indanes via Formal [3 + 2] Cycloaddition of Benzyl Alcohols with Olefins》.Safety of Ethyltriphenylphosphonium bromide The author mentioned the following in the article:

An environmentally friendly and high diastereoselective method for synthesizing indanes was developed via a metastable-state photoacid system containing catalytic protonated merocyanine (MEH). Under visible-light irradiation, MEH yields a metastable spiro structure and liberated protons, which facilitated the formation of carbocations from benzyl alcs., thus delivering diverse mols. in the presence of various nucleophiles. Mainly, a variety of indanes was easily obtained from benzyl alcs. and olefins and water was the only byproduct. In addition to this study using Ethyltriphenylphosphonium bromide, there are many other studies that have used Ethyltriphenylphosphonium bromide(cas: 1530-32-1Safety of Ethyltriphenylphosphonium bromide) was used in this study.

Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. It is also used as catalysts in the synthesis of certain organic compounds and as a pharmaceutical intermediate.Safety of Ethyltriphenylphosphonium bromide

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Zhang, Yulong; He, Jun; Song, Peihong; Wang, You; Zhu, Shaolin published their research in CCS Chemistry in 2021. The article was titled 《Ligand-enabled NiH-catalyzed migratory hydroamination: chain walking as a strategy for regiodivergent/regioconvergent remote sp3C-H amination》.Product Details of 1530-32-1 The article contains the following contents:

A nondirected, remote sp3C-H amination process with predictable and switchable regioselectivity was reported. This reaction used a nickel hydride-catalyzed remote relay hydroamination strategy in which an aliphatic amino group was installed at a position far from the original C=C bond present in all unsaturated hydrocarbon substrates. Depending on the choice of ligand, either terminal or benzylic functionalization products were obtained with excellent levels of regioselectivity. It was shown that an alkyl bromide could also be used as an olefin precursor when using Mn0 as a reductant. The utility of this transformation was further highlighted by the regioconvergent migratory hydroamination of isomeric mixtures of olefins forming single isomers of value-added benzylic or linear amines. The experimental part of the paper was very detailed, including the reaction process of Ethyltriphenylphosphonium bromide(cas: 1530-32-1Product Details of 1530-32-1)

Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. It is also used as catalysts in the synthesis of certain organic compounds and as a pharmaceutical intermediate.Product Details of 1530-32-1

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

The author of 《Palladium-Catalyzed Dialkylation of C-C Triple Bonds: Access to Multi-Functionalized Indenes》 were Liu, Xiao-Wei; Li, Shu-Sen; Dai, Dong-Ting; Zhao, Meng; Shan, Cui-Cui; Xu, Yun-He; Loh, Teck-Peng. And the article was published in Organic Letters in 2019. SDS of cas: 1530-32-1 The author mentioned the following in the article:

A palladium-catalyzed dialkylation of 1,3-dien-5-ynes was developed using alkenyl double bonds as the initiator and terminator for the synthesis of functionalized indene derivatives The reactions were performed under mild reaction conditions, affording the corresponding multi-substituted indene derivatives in high efficiency via unprecedented 5-endo cyclization and alkylation processes. The substituent location at the alkenyl double bond was essential for the chemoselective synthesis of the indene and naphthalene derivatives, resp. In addition to this study using Ethyltriphenylphosphonium bromide, there are many other studies that have used Ethyltriphenylphosphonium bromide(cas: 1530-32-1SDS of cas: 1530-32-1) was used in this study.

Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. CatOnium ETPB is also used as catalysts in the synthesis of certain organic compounds.SDS of cas: 1530-32-1

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary