Category: 91-00-9

Authors Shelp, RA; Ciro, A; Pu, YG; Merchant, RR; Hughes, JME; Walsh, PJ in ROYAL SOC CHEMISTRY published article about in [Shelp, Russell A.; Ciro, Anthony; Pu, Youge; Walsh, Patrick J.] Univ Penn, Dept Chem, Roy & Diana Vagelos Labs, 231 South 34th St, Philadelphia, PA 19104 USA; [Merchant, Rohan R.] Merck & Co Inc, Dept Discovery Chem, San Francisco, CA 94080 USA; [Hughes, Jonathan M. E.] Merck & Co Inc, Dept Proc Res & Dev, Rahway, NJ 07065 USA in 2021, Cited 41. HPLC of Formula: C13H13N. The Name is Diphenylmethanamine. Through research, I have a further understanding and discovery of 91-00-9

We report a 3-component reaction between N-benzyl ketimines, [1.1.1]propellane, and pinacol boronates to generate benzylamine bicyclo[1.1.1]pentane (BCP) pinacol boronates. These structures are analogous to highly sought diarylmethanamine cores, which are common motifs in bioactive molecules. We demonstrate the versatility of the boronate ester handle via downstream functionalization through a variety of reactions, including a challenging Pd-catalyzed (hetero)arylation that exhibits a broad substrate scope. Together, these methods enable the synthesis of high-value BCP benzylamines which are inaccessible by existing methods. Furthermore, we demonstrate the successful application of these newly developed (hetero)arylation conditions to a variety of challenging tertiary pinacol boronates, including nitrogen-containing heterocycles, 1,1-disubstituted cyclopropanes, and other BCP cores.

HPLC of Formula: C13H13N. Welcome to talk about 91-00-9, If you have any questions, you can contact Shelp, RA; Ciro, A; Pu, YG; Merchant, RR; Hughes, JME; Walsh, PJ or send Email.

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Amide – Wikipedia,
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Product Details of 91-00-9. In 2019 SYNTHESIS-STUTTGART published article about ONE-POT SYNTHESIS; OXIDATIVE CARBONYLATION; EFFICIENT CONVERSION; TRISUBSTITUTED UREAS; BIOLOGICAL-ACTIVITY; CARBOXYLIC-ACIDS; AMINES; FACILE; INHIBITORS; DESIGN in [Singh, Anoop S.; Agrahari, Anand K.; Singh, Sumit K.; Yadav, Mangal S.; Tiwari, Vinod K.] Banaras Hindu Univ, Inst Sci, Dept Chem, Varanasi 22100, Uttar Pradesh, India in 2019, Cited 83. The Name is Diphenylmethanamine. Through research, I have a further understanding and discovery of 91-00-9.

The good leaving tendency of the benzotriazole moiety has been exploited for the synthesis of symmetric, unsymmetric, N-acyl, and cyclic ureas in good yields from N-acylbenzotriazoles by treating the latter with various amines in the presence of TMSN N in a sealed tube. The salient features of the devised protocol includes the high-yield, mild, metal-free, one-pot reaction conditions, and short reaction time. Furthermore, in many cases, no column chromatography is required for the purification.

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An article General synthesis of primary amines via reductive amination employing a reusable nickel catalyst WOS:000455845400014 published article about AQUEOUS AMMONIA; SELECTIVE HYDROGENATION; IRON CATALYSTS; ALKYLATION; ALCOHOLS; KETONES; ACIDS; FURFURYLAMINE; NANOPARTICLES; NITROARENES in [Hahn, G.; Kempe, R.] Univ Bayreuth, Chair Inorgan Chem II Catalyst Design, Bayreuth, Germany; [Kunnas, P.; de Jonge, N.] INM Leibniz Inst New Mat, Saarbrucken, Germany; [de Jonge, N.] Saarland Univ, Dept Phys, Saarbrucken, Germany in 2019, Cited 54. Name: Diphenylmethanamine. The Name is Diphenylmethanamine. Through research, I have a further understanding and discovery of 91-00-9

Reusable catalysts based on earth-abundant metals with a broad applicability in organic synthesis are a key to a more sustainable production of fine chemicals, pharmaceuticals and agrochemicals. Herein, we report on a nanostructured nickel catalyst for the general and selective synthesis of primary amines via reductive amination, employing ammonia dissolved in water. Our catalyst, which operates at low temperature and pressure, is highly active, reusable and easy to handle. The synthesis from a specific nickel complex and gamma-Al2O3 is straightforward, with the ligand-metal combination of this complex being crucial. Aldehydes (including purely aliphatic ones), aryl-alkyl, dialkyl and diaryl ketones can all be converted smoothly into primary amines. In addition, the amination of pharmaceuticals, bioactive compounds and natural products is demonstrated. Many functional groups-including hydrogenation-sensitive examples-are tolerated. We expect that our findings will inspire others to develop reusable and nanostructured earth-abundant metal catalysts for complex organic transformations.

Name: Diphenylmethanamine. Welcome to talk about 91-00-9, If you have any questions, you can contact Hahn, G; Kunnas, P; de Jonge, N; Kempe, R or send Email.

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An article Total synthesis of Met(10)-teixobactin WOS:000475998200009 published article about STAPHYLOCOCCUS-AUREUS MRSA; POTENT TEIXOBACTIN ANALOGS; ANTIBACTERIAL ACTIVITY; IN-VITRO; ENDURACIDIDINE; SUBSTITUTION; RESIDUES; DESIGN in [Gunjal, Vidya B.; Reddy, D. Srinivasa] CSIR Natl Chem Lab, Organ Chem Div, Dr Homi Bhabha Rd, Pune 411008, Maharashtra, India; [Gunjal, Vidya B.; Reddy, D. Srinivasa] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India in 2019.0, Cited 41.0. The Name is Diphenylmethanamine. Through research, I have a further understanding and discovery of 91-00-9. Computed Properties of C13H13N

The total synthesis of cyclic depsipeptide Met(10)-teixobactin in solution-phase is described. Teixobactin is a structurally and mechanistically novel antimicrobial peptidic natural product with very impressive activities against Gram-positive pathogens. It happens to possess an L-allo-enduracididine (End) residue as part of macrocyclic ring which is not readily accessible. In this report, we have used serine ligation strategy as the key step to prepare an analogue of teixobactin where End being replaced with a readily available amino acid methionine. (C) 2019 Elsevier Ltd. All rights reserved.

Computed Properties of C13H13N. Welcome to talk about 91-00-9, If you have any questions, you can contact Gunjal, VB; Reddy, DS or send Email.

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Category: amides-buliding-blocks. I found the field of Chemistry very interesting. Saw the article Pro-Phe Derivatives as Organocatalysts in Asymmetric Aldol Reaction published in 2021, Reprint Addresses Yolacan, C (corresponding author), Yildiz Tech Univ, Dept Chem, Davutpasa Campus, TR-34010 Istanbul, Turkey.. The CAS is 91-00-9. Through research, I have a further understanding and discovery of Diphenylmethanamine.

The aldol reaction which is the most important one among the C-C bond forming reactions, is widely used by synthetic organic chemists to obtain beta-hydroxycarbonyl compounds which are important starting components for biologically active compounds in optically pure form. In this research, five Pro-Phe derivatives were synthesized by simple amidation reactions and characterized by their spectral data. Their catalytic activities in asymmetric aldol reaction were investigated. The catalytic activity studies were performed with aliphatic ketones and various aromatic aldehydes. Especially, (S)methyl 3-mercapto-2-(S)-3-phenyl-2-((S)-pyrrolidine-2-carboxamido)propanamido)propanoate showed good catalytic activities in water at 0 degrees C in the presence of p-nitrobenzoic acid cocatalyst. The enantioselectivities were up to 90.4%, the diastereomeric ratios were up to 97/3 and yields were 99%. The results showed that these organocatalysts were promising organocatalysts for aldol reaction. Besides, this catalyst showed its best catalytic activities in water which is also an important contribution to green chemistry requirements.

Category: amides-buliding-blocks. Welcome to talk about 91-00-9, If you have any questions, you can contact Karaoglu, M; Aydogan, F; Yolacan, C or send Email.

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I found the field of Chemistry; Science & Technology – Other Topics very interesting. Saw the article An efficient way for the N-formylation of amines by inorganic-ligand supported iron catalysis published in 2020. SDS of cas: 91-00-9, Reprint Addresses Yu, H; Han, S (corresponding author), Shanghai Inst Technol, Sch Chem & Environm Engn, 100 Haiquan Rd, Shanghai 201418, Peoples R China.; Yu, H; Wei, YG (corresponding author), Tsinghua Univ, Dept Chem, Minist Educ, Key Lab Organ Optoelect & Mol Engn, Beijing 100084, Peoples R China.; Wei, YG (corresponding author), Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China.. The CAS is 91-00-9. Through research, I have a further understanding and discovery of Diphenylmethanamine

The first example of an inorganic-ligand supported iron(iii) catalysed coupling of formic acid and amines to form formamides is reported. The pure inorganic catalyst (NH4)(3)[FeMo6O18(OH)(6)] (1), which consists of a central Fe-III single-atomic core supported within a cycle-shaped inorganic ligand consisting of six (MoO6)-O-VI octahedra, shows excellent activity and selectivity, and avoids the use of complicated/commercially unavailable organic ligands. Various primary amines and secondary amines have been successfully transformed into the corresponding formamides under mild conditions, and the formylation of primary diamines has also been achieved for the first time. The Fe catalyst 1 can be reused several times without appreciable loss of activity.

SDS of cas: 91-00-9. Welcome to talk about 91-00-9, If you have any questions, you can contact Wu, ZK; Zhai, YY; Zhao, WS; Wei, ZY; Yu, H; Han, S; Wei, YG or send Email.

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An article An unsymmetrical binuclear iminopyridine-iron complex and its catalytic isoprene polymerization WOS:000555234200027 published article about 3,4-SELECTIVE LIVING POLYMERIZATION; 1,3-BUTADIENE POLYMERIZATION; METAL; IRON(III); 3,4-POLYMERIZATION; REGIOSELECTIVITY; 1,3-DIENES; BUTADIENE; LIGANDS; SYSTEMS in [Wang, Liang; Wang, Xiaowu; Hou, Hongbin; Zhu, Guangqian; Han, Zhenyu; Yang, Weiying; Chen, Xiao; Wang, Qinggang] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Key Lab Biobased Mat, Qingdao 266101, Peoples R China; [Zhu, Guangqian; Han, Zhenyu; Yang, Weiying] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China in 2020.0, Cited 51.0. The Name is Diphenylmethanamine. Through research, I have a further understanding and discovery of 91-00-9. Safety of Diphenylmethanamine

A series of chloride-bridged unsymmetrical mixed Fe(ii)-HS/Fe(ii)-LS binuclear structures has been prepared and characterized. Upon activation with MAO, highly efficient catalytic polymerization of isoprene was achieved, delivering an ultra-high molecular weight (catalyst loading = 2.5 ppm,M-n= 1.8 x 10(6)g mol(-1),M-w/M-n= 1.4).

Safety of Diphenylmethanamine. Bye, fridends, I hope you can learn more about C13H13N, If you have any questions, you can browse other blog as well. See you lster.

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Amide – Wikipedia,
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Authors Karasik, AA; Strelnik, ID; Musina, EI; Dayanova, IR; Elistratova, JG; Mustafina, AR; Sinyashin, OG in TAYLOR & FRANCIS LTD published article about PHOSPHINO AMINO-ACIDS; LIGANDS; CATALYSTS in [Karasik, Andrey A.; Strelnik, Igor D.; Musina, Elvira I.; Dayanova, Irina R.; Elistratova, Julia G.; Mustafina, Asiya R.; Sinyashin, Oleg G.] RAS, FRC Kazan Sci Ctr, Arbuzov Inst Organ & Phys Chem, Kazan, Russia in 2019.0, Cited 23.0. Product Details of 91-00-9. The Name is Diphenylmethanamine. Through research, I have a further understanding and discovery of 91-00-9

Cyclic aminomethylphosphines in general and 1,5-diaza-3,7-dihposphacyclooctanes in particular are widely used for the design of d(10)-metal complexes with catalytic or luminescent properties. 1,5-Diaza-3,7-diphosphacyclooctanes are chelating ligands towards Ni subgroup metals and chelating or bridging ligands towards copper subgroup metals. These ligands can be utilized for the design of polynuclear complexes with stimuli-responsive luminescence. Nowadays several complexes based on 1,5-diaza-3,7-diphosphacyclooctanes demonstrating stimuli-response of emission towards organic substrates or temperature are known. Some of the gold(I) complexes are able to sensitize the luminescent anionic rhenium cluster. Copper(I) complexes display rather strong luminescence with quantum yields 20-40%. [GRAPHICS] .

Product Details of 91-00-9. Welcome to talk about 91-00-9, If you have any questions, you can contact Karasik, AA; Strelnik, ID; Musina, EI; Dayanova, IR; Elistratova, JG; Mustafina, AR; Sinyashin, OG or send Email.

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Amide – Wikipedia,
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Authors Chen, DH; Sun, WT; Zhu, CJ; Lu, GS; Wu, DP; Wang, AE; Huang, PQ in WILEY-V C H VERLAG GMBH published article about in [Chen, Dong-Huang; Sun, Wei-Ting; Zhu, Cheng-Jie; Lu, Guang-Sheng; Wu, Dong-Ping; Wang, Ai-E; Huang, Pei-Qiang] Xiamen Univ, Dept Chem, Coll Chem & Chem Engn, Xiamen 361005, Fujian, Peoples R China; [Chen, Dong-Huang; Sun, Wei-Ting; Zhu, Cheng-Jie; Lu, Guang-Sheng; Wu, Dong-Ping; Wang, Ai-E; Huang, Pei-Qiang] Xiamen Univ, Fujian Prov Key Lab Chem Biol, Coll Chem & Chem Engn, Xiamen 361005, Fujian, Peoples R China; [Wang, Ai-E; Huang, Pei-Qiang] Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China in 2021.0, Cited 89.0. Quality Control of Diphenylmethanamine. The Name is Diphenylmethanamine. Through research, I have a further understanding and discovery of 91-00-9

The combination of transition-metal catalysis and organocatalysis increasingly offers chemists opportunities to realize diverse unprecedented chemical transformations. By combining iridium with chiral thiourea catalysis, direct enantioselective reductive cyanation and phosphonylation of secondary amides have been accomplished for the first time for the synthesis of enantioenriched chiral alpha-aminonitriles and alpha-aminophosphonates. The protocol is highly efficient and enantioselective, providing a novel route to the synthesis of optically active alpha-functionalized amines from the simple, readily available feedstocks. In addition, the reactions are scalable and the thiourea catalyst can be recycled and reused.

Quality Control of Diphenylmethanamine. Bye, fridends, I hope you can learn more about C13H13N, If you have any questions, you can browse other blog as well. See you lster.

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In 2020.0 APPL ORGANOMET CHEM published article about CRYSTAL-STRUCTURE; ALKYLATION; ALCOHOLS; AMINATION; DEHYDROGENATION; SECONDARY; KETONES; IMINES; 5-(2-PYRIDYLMETHYLENE)HYDANTOIN; HYDROAMINATION in [Ruiz-Castaneda, Margarita; Rodriguez, Ana M.; Manzano, Blanca R.; Jalon, Felix A.] Univ Castilla La Mancha, Fac Quim, Dept Quim Inorgan Organ & Bioquim, IRICA, Avda Camilo J Cela 10, Ciudad Real 13071, Spain; [Aboo, Ahmed H.; Xiao, Jianliang] Univ Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, England; [Espino, Gustavo] Univ Burgos, Fac Ciencias, Dept Quim, Plaza Misael Banuelos S-N, Burgos 09001, Spain in 2020.0, Cited 70.0. The Name is Diphenylmethanamine. Through research, I have a further understanding and discovery of 91-00-9. Category: amides-buliding-blocks

The development of efficient and eco-friendly methods for the synthesis of elaborate amines is highly desired as they are valuable chemicals. The catalytic alkylation of amines using alcohols as alkylating agents, through the so-called borrowing hydrogen process, satisfies several of the principles of green chemistry. In this paper, four neutral half-sandwich complexes of Ru(II), Rh(III), and Ir(III) have been synthesized and tested as catalysts in theN-benzylation of amines with benzyl alcohol. The new derivatives contain aN(boolean AND)N ‘ anionic ligand derived from 5-(pyridin-2-ylmethylene)hydantoin (Hpyhy) that has never been tested in metal complexes with catalytic applications. In particular, the Ir derivatives, [(Cp*)IrX(pyhy)] (X = Cl or H), exhibit high activity along with good selectivity in the process. Indeed, the scope of the optimized protocol has been proved in the benzylation of several primary and secondary amines. The selectivity towards monoalkylated or dialkylated amines has been tuned by adjusting the amine:alcohol ratio and the reaction time. Experimental results support a mechanism consisting of three consecutive steps, two of which are Ir catalyzed, and a favorable condensation step without the assistance of the catalyst. Moreover, an unproductive competitive pathway can operate when the reaction is performed in open-air vessels, due to the irreversible release of H-2. This route is hampered when the reaction is carried out in close vessels, likely because the release of H(2)is reversed through metal-based heterolytic cleavage. From our viewpoint, these results show the potential of the new catalysts in a very attractive and promising methodology for the synthesis of amines.

Category: amides-buliding-blocks. Bye, fridends, I hope you can learn more about C13H13N, If you have any questions, you can browse other blog as well. See you lster.

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Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics