Category: 221012-82-4

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: (R)-2,2′,6,6′-Tetramethoxy-4,4′-bis(diphenylphosphino)-3,3′-bipyridine, is researched, Molecular C38H34N2O4P2, CAS is 221012-82-4, about Highly effective chiral dipyridylphosphine ligands: Synthesis, structural determination, and applications in the Ru-catalyzed asymmetric hydrogenation reactions.SDS of cas: 221012-82-4.

The synthesis of the new heteroaromatic chiral diphosphine ligands (R) and (S)-(P-phos) [P- phos = 2,2′,6,6′-tetramethoxy-4,4′-bis(diphenylphosphino)-3,3′-bipyridine] was carried out by a standard synthetic protocol ending up with an Ullmann coupling, followed by resolution of the racemic product. The ligands display an axial chirality due to atropisomery-, analogous to that observed in the parent ligand MeO-BIPHEP. Well-defined ruthenium(II) catalysts were prepared and employed to catalyze the hydrogenation of a prochiral olefins of pharmaceutical relevance and various β-ketoesters.

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Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 221012-82-4, is researched, Molecular C38H34N2O4P2, about Rhodium-Catalyzed Asymmetric Allylic Substitution with Boronic Acid Nucleophiles, the main research direction is cyclopentenediol stereoselective allylic substitution arylboronic acid.Electric Literature of C38H34N2O4P2.

An enantio-, regio-, and diastereoselective rhodium(I)-catalyzed desymmetrization of a meso-cyclic allylic dicarbonate with organoboronic acid nucleophiles is described. The rhodium(I) catalyst formed in situ from [Rh(cod)OH]2 and Xyl-P-PHOS allowed the SN2′ allylic substitution product to be obtained with a range of arylboronic acids in enantiomeric excesses of up to 92% with regioselectivities of up to >20:1.

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Niu, Weiling; Chen, Li; Hu, Jiayuan; Chen, Hua; Li, Xianjun published the article 《Asymmetric hydroformylation of styrene catalyzed by P-Phos-Rh complexes [P-Phos = 4,4′,6,6′-tetramethoxy-2,2′-bis(diphenylphosphino)-1,1′-bipyridine]》. Keywords: styrene asym hydroformylation catalyst rhodium chiral diphosphine.They researched the compound: (R)-2,2′,6,6′-Tetramethoxy-4,4′-bis(diphenylphosphino)-3,3′-bipyridine( cas:221012-82-4 ).Computed Properties of C38H34N2O4P2. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:221012-82-4) here.

Rh complex was prepared by complexation of (R)-P-Phos with the available Rh precursor and used for the asym. hydroformylation of styrene. The effects of total pressure, temperature, and the ratio of phosphine/Rh on catalytic activity, chemo- and enantioselectivity were discussed. (R)-P-Phos-Rh showed higher activity and regioselectivity and the enantioselectivity was as much as that catalyzed by -BINAP-Rh (BINAP = 2,2′-di(diphenylphosphino)-1,1′-bipyridine) in the in situ asym. hydroformylation of styrene.

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Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 221012-82-4, is researched, Molecular C38H34N2O4P2, about Enantioselective bis-alkoxycarbonylation of styrene catalyzed by novel chiral dipyridylphosphine cationic palladium(II) complexes, the main research direction is enantioselective bisalkoxycarbonylation styrene chiral dipyridylphosphine cationic palladium complex catalyst; asym alkoxycarbonylation styrene chiral dipyridylphosphine cationic palladium complex catalyst.Formula: C38H34N2O4P2.

The preparation of new palladium complexes that are composed of a series of chiral dipyridylphosphines have been described. The structure of the complex [{(R)-1}Pd(H2O)2](OTf)2 was unambiguously determined by single-crystal X-ray diffractometry. These complexes were found to be effective in the asym. bis-methoxycarbonylation of styrene, reaching up to 84% e.e. and 79% chemoselectivity for dimethyl-2-phenylsuccinate (DMPS) under the optimal conditions. In addition, the complexes exhibited almost identical enantioselectivity on DMPS.

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Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 221012-82-4, is researched, Molecular C38H34N2O4P2, about Asymmetric hydrogenation of isobutyrophenone Using a [(diphosphine)RuCl2(1,4-diamine)] catalyst, the main research direction is ruthenium diphosphine diamine complex preparation hydrogenation catalyst; crystal structure ruthenium diphosphine diamine complex; ketone hydrogenation ruthenium diphosphine diamine complex catalyst.Synthetic Route of C38H34N2O4P2.

The use of three chiral 1,4-diamines in the [(diphosphine)RuCl2(diamine)] catalyst system is demonstrated in the hydrogenation of acetophenone. The use of a 1,4-diamine offers unique properties that allow tuning of the catalyst system. These include the 1st example of the use of a racemic diamine in combination with a chiral phosphine, which gives 95% ee in the hydrogenation of isobutyrophenone.

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Quinoxaline – Wikipedia,
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SDS of cas: 221012-82-4. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: (R)-2,2′,6,6′-Tetramethoxy-4,4′-bis(diphenylphosphino)-3,3′-bipyridine, is researched, Molecular C38H34N2O4P2, CAS is 221012-82-4, about 3,3′-Bipyridine, 4,4′-bis(diphenylphosphino)-2,2′,6,6′-tetramethoxy-, (3R)-; 3,3′-Bipyridine, 4,4′-bis(diphenylphosphino)-2,2′,6,6′-tetramethoxy-, (3S)-. Author is Srinivasarao, Madduri.

Properties and applications of 3,3′-bipyridine, 4,4′-bis(diphenylphosphino)-2,2′,6,6′-tetramethoxy-, (3R)-; 3,3′-bipyridine, 4,4′-bis(diphenylphosphino)-2,2′,6,6′-tetramethoxy-, (3S)-, a chiral biaryl bisphosphine ligands used for high activity and selectivity in catalytic hydrogenation of ketones, β-ketoesters, α,β-unsaturated carbonyl compounds, quinolines; transfer hydrogenation, Pauson-Khand-type reactions, carbonylation and other reductions are reviewed.

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The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (R)-2,2′,6,6′-Tetramethoxy-4,4′-bis(diphenylphosphino)-3,3′-bipyridine( cas:221012-82-4 ) is researched.Electric Literature of C38H34N2O4P2.Menard, Frederic; Perez, David; Sustac Roman, Daniela; Chapman, Timothy M.; Lautens, Mark published the article 《Ligand-Controlled Selectivity in the Desymmetrization of meso Cyclopenten-1,4-diols via Rhodium(I)-Catalyzed Addition of Arylboronic Acids》 about this compound( cas:221012-82-4 ) in Journal of Organic Chemistry. Keywords: meso cyclopentene dicarbonate boronic acid rhodium catalyst allylic substitution; arylcyclopentenol chiral ligand controlled regioselective stereoselective preparation. Let’s learn more about this compound (cas:221012-82-4).

A highly enantioselective desymmetrization of meso cyclopent-2-ene-1,4-diethyl dicarbonates has been developed using a Rh-catalyzed asym. allylic substitution. Depending on the type of ligand used, each of two regioisomeric products can be obtained in good yield and excellent enantioselectivity. Under rhodium(I) catalysis, bisphosphine P-Phos ligands form trans-1,2-arylcyclopentenols as the major product, whereas Segphos ligands lead predominantly to trans-1,4-arylcyclopentenols.

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Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 221012-82-4, is researched, SMILESS is COC(C=C1P(C2=CC=CC=C2)C3=CC=CC=C3)=NC(OC)=C1C4=C(OC)N=C(OC)C=C4P(C5=CC=CC=C5)C6=CC=CC=C6, Molecular C38H34N2O4P2Journal, Synthesis called Synthesis of homoallylic alcohols via Lewis acid assisted enantioselective desymmetrization, Author is Yu, Bing; Menard, Frederic; Isono, Naohiro; Lautens, Mark, the main research direction is butenediol carbonate arylboronate enantioselective allylic substitution rhodium catalyst; homoallylic alc asym synthesis.Application of 221012-82-4.

A highly enantioselective allylic substitution of (Z)-but-2-ene-1,4-diol derivatives was developed using a Rh(I) catalyst and arylboronates as nucleophiles. The reaction yields versatile homoallylic alcs. from readily available linear bis-carbonates.

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Reference:
Quinoxaline – Wikipedia,
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Maj, Anna M.; Suisse, Isabelle; Hardouin, Christophe; Agbossou-Niedercorn, Francine published an article about the compound: (R)-2,2′,6,6′-Tetramethoxy-4,4′-bis(diphenylphosphino)-3,3′-bipyridine( cas:221012-82-4,SMILESS:COC(C=C1P(C2=CC=CC=C2)C3=CC=CC=C3)=NC(OC)=C1C4=C(OC)N=C(OC)C=C4P(C5=CC=CC=C5)C6=CC=CC=C6 ).Recommanded Product: 221012-82-4. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:221012-82-4) through the article.

The asym. hydrogenation of a series of quinolines substituted by a variety of functionalized groups linked to the C2 carbon atom is providing access to optically enriched 2-functionalized 1,2,3,4-tetrahydroquinolines in the presence of in situ generated catalysts from [Ir(cod)Cl]2, a bisphosphine, and iodine. The enantioselectivity levels were as high as 96% ee.

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Category: quinoxaline. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: (R)-2,2′,6,6′-Tetramethoxy-4,4′-bis(diphenylphosphino)-3,3′-bipyridine, is researched, Molecular C38H34N2O4P2, CAS is 221012-82-4, about Air-Stable Catalysts for Highly Efficient and Enantioselective Hydrogenation of Aromatic Ketones. Author is Wu, Jing; Chen, Hua; Kwok, Waihim; Guo, Rongwei; Zhou, Zhongyuan; Yeung, Chihung; Chan, Albert S. C..

A series of chiral trans-[RuCl2(bipyridinediylbisphosphine)(1,2-diamine)] complexes have been synthesized and characterized by NMR and single-crystal X-ray diffraction studies. These Ru complexes combined with (CH3)3COK in 2-propanol formed a very effective catalyst system for the hydrogenation of a diverse range of simple aromatic ketones with high activity (substrate-to-catalyst ratio up to 100,000) and excellent enantioselectivity (up to >99.9%). The catalyst system was also found to be stable in solution even under a normal atm.

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Reference:
Quinoxaline – Wikipedia,
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