Category: 1086138-36-4

HPLC of Formula: 1086138-36-4. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine, is researched, Molecular C44H69NP2, CAS is 1086138-36-4, about Erbium-Catalyzed Regioselective Isomerization-Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions. Author is Liu, Xin; Longwitz, Lars; Spiegelberg, Brian; Toenjes, Jan; Beweries, Torsten; Werner, Thomas.

Herein, we report an efficient isomerization-transfer hydrogenation reaction sequence based on a cobalt pincer catalyst (1 mol%), which allows the synthesis of a series of anti-Markovnikov alcs. from terminal and internal epoxides under mild reaction conditions (≤55°, 8 h) at low catalyst loading. The reaction proceeds by Lewis acid (3 mol % Er(OTf)3)-catalyzed epoxide isomerization and subsequent cobalt-catalyzed transfer hydrogenation using ammonia borane as the hydrogen source. The general applicability of this methodol. is highlighted by the synthesis of 43 alcs. from epoxides. A variety of terminal (23 examples) and 1,2-disubstituted internal epoxides (14 examples) bearing different functional groups are converted to the desired anti-Markovnikov alcs. in excellent selectivity and yields of up to 98%. For selected examples, it is shown that the reaction can be performed on a preparative scale up to 50 mmol. Notably, the isomerization step proceeds via the most stable carbocation. Thus, the regiochem. is controlled by stereoelectronic effects. As a result, in some cases, rearrangement of the carbon framework is observed when tri- and tetra-substituted epoxides (6 examples) are converted. A variety of functional groups are tolerated under the reaction conditions even though aldehydes and ketones are also reduced to the resp. alcs. under the reaction conditions. Mechanistic studies and control experiments were used to investigate the role of the Lewis acid in the reaction. Besides acting as the catalyst for the epoxide isomerization, the Lewis acid was found to facilitate the dehydrogenation of the hydrogen donor, which enhances the rate of the transfer hydrogenation step. These experiments addnl. indicate the direct transfer of hydrogen from the amine borane in the reduction step.

Here is just a brief introduction to this compound(1086138-36-4)HPLC of Formula: 1086138-36-4, more information about the compound(Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine) is in the article, you can click the link below.

Reference:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

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: 1086138-36-4, is researched, Molecular C44H69NP2, about Erbium-Catalyzed Regioselective Isomerization-Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions, the main research direction is tandem erbium catalyst regioselective isomerization cobalt transfer hydrogenation epoxide; synthesis anti Markovnikov alc.Synthetic Route of C44H69NP2.

Herein, we report an efficient isomerization-transfer hydrogenation reaction sequence based on a cobalt pincer catalyst (1 mol%), which allows the synthesis of a series of anti-Markovnikov alcs. from terminal and internal epoxides under mild reaction conditions (≤55°, 8 h) at low catalyst loading. The reaction proceeds by Lewis acid (3 mol % Er(OTf)3)-catalyzed epoxide isomerization and subsequent cobalt-catalyzed transfer hydrogenation using ammonia borane as the hydrogen source. The general applicability of this methodol. is highlighted by the synthesis of 43 alcs. from epoxides. A variety of terminal (23 examples) and 1,2-disubstituted internal epoxides (14 examples) bearing different functional groups are converted to the desired anti-Markovnikov alcs. in excellent selectivity and yields of up to 98%. For selected examples, it is shown that the reaction can be performed on a preparative scale up to 50 mmol. Notably, the isomerization step proceeds via the most stable carbocation. Thus, the regiochem. is controlled by stereoelectronic effects. As a result, in some cases, rearrangement of the carbon framework is observed when tri- and tetra-substituted epoxides (6 examples) are converted. A variety of functional groups are tolerated under the reaction conditions even though aldehydes and ketones are also reduced to the resp. alcs. under the reaction conditions. Mechanistic studies and control experiments were used to investigate the role of the Lewis acid in the reaction. Besides acting as the catalyst for the epoxide isomerization, the Lewis acid was found to facilitate the dehydrogenation of the hydrogen donor, which enhances the rate of the transfer hydrogenation step. These experiments addnl. indicate the direct transfer of hydrogen from the amine borane in the reduction step.

Compound(1086138-36-4)Synthetic Route of C44H69NP2 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine), if you are interested, you can check out my other related articles.

Reference:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

COA of Formula: C44H69NP2. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine, is researched, Molecular C44H69NP2, CAS is 1086138-36-4, about Synthons for carbide complex chemistry. Author is Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper.

The sterically accessible carbide complex, (Cy3P)Cl3RuC-PtCl(py)2, acts as a synthon for terminal and bridging carbide fragments that relocate to pincer and A-frame scaffolds upon ligand addition This concept, benefitting from coordination sphere selection as the concluding step, confronts traditional synthetic strategies and broadens the scope for carbide complexes.

Compound(1086138-36-4)COA of Formula: C44H69NP2 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine), if you are interested, you can check out my other related articles.

Reference:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Liu, Xin; Longwitz, Lars; Spiegelberg, Brian; Toenjes, Jan; Beweries, Torsten; Werner, Thomas researched the compound: Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine( cas:1086138-36-4 ).Reference of Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine.They published the article 《Erbium-Catalyzed Regioselective Isomerization-Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions》 about this compound( cas:1086138-36-4 ) in ACS Catalysis. Keywords: tandem erbium catalyst regioselective isomerization cobalt transfer hydrogenation epoxide; synthesis anti Markovnikov alc. We’ll tell you more about this compound (cas:1086138-36-4).

Herein, we report an efficient isomerization-transfer hydrogenation reaction sequence based on a cobalt pincer catalyst (1 mol%), which allows the synthesis of a series of anti-Markovnikov alcs. from terminal and internal epoxides under mild reaction conditions (≤55°, 8 h) at low catalyst loading. The reaction proceeds by Lewis acid (3 mol % Er(OTf)3)-catalyzed epoxide isomerization and subsequent cobalt-catalyzed transfer hydrogenation using ammonia borane as the hydrogen source. The general applicability of this methodol. is highlighted by the synthesis of 43 alcs. from epoxides. A variety of terminal (23 examples) and 1,2-disubstituted internal epoxides (14 examples) bearing different functional groups are converted to the desired anti-Markovnikov alcs. in excellent selectivity and yields of up to 98%. For selected examples, it is shown that the reaction can be performed on a preparative scale up to 50 mmol. Notably, the isomerization step proceeds via the most stable carbocation. Thus, the regiochem. is controlled by stereoelectronic effects. As a result, in some cases, rearrangement of the carbon framework is observed when tri- and tetra-substituted epoxides (6 examples) are converted. A variety of functional groups are tolerated under the reaction conditions even though aldehydes and ketones are also reduced to the resp. alcs. under the reaction conditions. Mechanistic studies and control experiments were used to investigate the role of the Lewis acid in the reaction. Besides acting as the catalyst for the epoxide isomerization, the Lewis acid was found to facilitate the dehydrogenation of the hydrogen donor, which enhances the rate of the transfer hydrogenation step. These experiments addnl. indicate the direct transfer of hydrogen from the amine borane in the reduction step.

In some applications, this compound(1086138-36-4)Reference of Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Meyer, Tim; Konrath, Robert; Kamer, Paul C. J.; Wu, Xiao-Feng researched the compound: Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine( cas:1086138-36-4 ).Formula: C44H69NP2.They published the article 《Pincer Ligand Enhanced Rhodium-Catalyzed Carbonylation of Formaldehyde: Direct Ethylene Glycol Production》 about this compound( cas:1086138-36-4 ) in Asian Journal of Organic Chemistry. Keywords: rhodium formaldehyde ethylene glycol carbonylation catalyst. We’ll tell you more about this compound (cas:1086138-36-4).

Formaldehyde is one of the most important bulk chems. and is produced on a million tone scale (52 million tons in 2017).[1] Since the middle of the last century, the challenge has remained to produce the valuable ethylene glycol (EG) directly from the C1 building block formaldehyde in a single step. In the systems reported so far, the reaction conditions were very harsh, often with pressures above 400 bar. However, under milder conditions, the selectivity was on the side of glycol aldehyde (GA) and the hydrogenation product methanol. Only traces of EG could be generated in the presence of a Rh catalyst. Herein, the authors describe a new Rh catalyst system with pincer ligand, which allows the direct one pot synthesis of EG from easy to handle paraformaldehyde (PFA) at remarkable mild conditions (70 bar, 100°C) and overcomes the aforementioned limitations with yield up to 40%.

In some applications, this compound(1086138-36-4)Formula: C44H69NP2 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine(SMILESS: P(CCNCCP(C12CC3CC(C2)CC(C3)C1)C45CC6CC(C5)CC(C6)C4)(C78CC9CC(C8)CC(C9)C7)C%10%11CC%12CC(C%11)CC(C%12)C%10,cas:1086138-36-4) is researched.Computed Properties of C5H5ClN2. The article 《Additive-Free Isomerization of Allylic Alcohols to Ketones with a Cobalt PNP Pincer Catalyst》 in relation to this compound, is published in Chemistry – A European Journal. Let’s take a look at the latest research on this compound (cas:1086138-36-4).

Catalytic isomerization of allylic alcs. in ethanol as a green solvent was achieved by using air and moisture stable cobalt (II) complexes in the absence of any additives. Under mild conditions, the cobalt PNP pincer complex substituted with Ph groups on the phosphorus atoms appeared to be the most active. High rates were obtained at 120°, even though the addition of one equivalent of base increases the speed of the reaction drastically. Although some evidence was obtained supporting a dehydrogenation-hydrogenation mechanism, it was proved that this is not the major mechanism. Instead, the cobalt hydride complex formed by dehydrogenation of ethanol was capable of double-bond isomerization through alkene insertion-elimination.

When you point to this article, it is believed that you are also very interested in this compound(1086138-36-4)Electric Literature of C44H69NP2 and due to space limitations, I can only present the most important information.

Reference:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

COA of Formula: C44H69NP2. 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: Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine, is researched, Molecular C44H69NP2, CAS is 1086138-36-4, about Catalytic Hydrogenation of Cyclic Carbonates: A Practical Approach from CO2 and Epoxides to Methanol and Diols. Author is Han, Zhaobin; Rong, Liangce; Wu, Jiang; Zhang, Lei; Wang, Zheng; Ding, Kuiling.

A highly efficient catalytic hydrogenation of cyclic carbonates was developed for the preparation of methanol with the cogeneration of the corresponding diols by using (PNP) Ru”” pincer complexes as the catalysts under relatively mild conditions. This process has provided a facile approach for the simultaneous production of two important bulk chems., methanol and EG, from ethylene carbonate, which is industrially available by reacting ethylene oxide with CO2. The coupling of the present catalytic system with the process of ethylene carbonate production in the omega process is expected to establish a new bridge from CO2 and ethylene oxide to methanol and EG. Apart from the clean production of diol, a big bonus of the present protocol is the efficient chem. utilization of CO2, which represents a distinct advantage in terms of sustainability over the omega process, which gives back CO2. Moreover, this catalytic system has also provided a potential process for the utilization of waste poly(propylene carbonate) as a resource to afford 1,2-propylene diol and methanol through hydrogenative depolymerization, and a convenient method for the preparation of deuterated methanol from CO2 and D2. A possible catalytic mechanism is proposed, in which the NH moiety of the ligand is demonstrated to be critically important in facilitating the reduction of the carbonate C=O bond through secondary coordination sphere interactions with substrates.

This literature about this compound(1086138-36-4)COA of Formula: C44H69NP2has given us a lot of inspiration, and I hope that the research on this compound(Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine) can be further advanced. Maybe we can get more compounds in a similar way.

Reference:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine(SMILESS: P(CCNCCP(C12CC3CC(C2)CC(C3)C1)C45CC6CC(C5)CC(C6)C4)(C78CC9CC(C8)CC(C9)C7)C%10%11CC%12CC(C%11)CC(C%12)C%10,cas:1086138-36-4) is researched.COA of Formula: C9H13NO2. The article 《Erbium-Catalyzed Regioselective Isomerization-Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions》 in relation to this compound, is published in ACS Catalysis. Let’s take a look at the latest research on this compound (cas:1086138-36-4).

Herein, we report an efficient isomerization-transfer hydrogenation reaction sequence based on a cobalt pincer catalyst (1 mol%), which allows the synthesis of a series of anti-Markovnikov alcs. from terminal and internal epoxides under mild reaction conditions (≤55°, 8 h) at low catalyst loading. The reaction proceeds by Lewis acid (3 mol % Er(OTf)3)-catalyzed epoxide isomerization and subsequent cobalt-catalyzed transfer hydrogenation using ammonia borane as the hydrogen source. The general applicability of this methodol. is highlighted by the synthesis of 43 alcs. from epoxides. A variety of terminal (23 examples) and 1,2-disubstituted internal epoxides (14 examples) bearing different functional groups are converted to the desired anti-Markovnikov alcs. in excellent selectivity and yields of up to 98%. For selected examples, it is shown that the reaction can be performed on a preparative scale up to 50 mmol. Notably, the isomerization step proceeds via the most stable carbocation. Thus, the regiochem. is controlled by stereoelectronic effects. As a result, in some cases, rearrangement of the carbon framework is observed when tri- and tetra-substituted epoxides (6 examples) are converted. A variety of functional groups are tolerated under the reaction conditions even though aldehydes and ketones are also reduced to the resp. alcs. under the reaction conditions. Mechanistic studies and control experiments were used to investigate the role of the Lewis acid in the reaction. Besides acting as the catalyst for the epoxide isomerization, the Lewis acid was found to facilitate the dehydrogenation of the hydrogen donor, which enhances the rate of the transfer hydrogenation step. These experiments addnl. indicate the direct transfer of hydrogen from the amine borane in the reduction step.

This literature about this compound(1086138-36-4)Electric Literature of C44H69NP2has given us a lot of inspiration, and I hope that the research on this compound(Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine) can be further advanced. Maybe we can get more compounds in a similar way.

Reference:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

Liu, Xin; Longwitz, Lars; Spiegelberg, Brian; Toenjes, Jan; Beweries, Torsten; Werner, Thomas published an article about the compound: Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine( cas:1086138-36-4,SMILESS:P(CCNCCP(C12CC3CC(C2)CC(C3)C1)C45CC6CC(C5)CC(C6)C4)(C78CC9CC(C8)CC(C9)C7)C%10%11CC%12CC(C%11)CC(C%12)C%10 ).Formula: C44H69NP2. 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:1086138-36-4) through the article.

Herein, we report an efficient isomerization-transfer hydrogenation reaction sequence based on a cobalt pincer catalyst (1 mol%), which allows the synthesis of a series of anti-Markovnikov alcs. from terminal and internal epoxides under mild reaction conditions (≤55°, 8 h) at low catalyst loading. The reaction proceeds by Lewis acid (3 mol % Er(OTf)3)-catalyzed epoxide isomerization and subsequent cobalt-catalyzed transfer hydrogenation using ammonia borane as the hydrogen source. The general applicability of this methodol. is highlighted by the synthesis of 43 alcs. from epoxides. A variety of terminal (23 examples) and 1,2-disubstituted internal epoxides (14 examples) bearing different functional groups are converted to the desired anti-Markovnikov alcs. in excellent selectivity and yields of up to 98%. For selected examples, it is shown that the reaction can be performed on a preparative scale up to 50 mmol. Notably, the isomerization step proceeds via the most stable carbocation. Thus, the regiochem. is controlled by stereoelectronic effects. As a result, in some cases, rearrangement of the carbon framework is observed when tri- and tetra-substituted epoxides (6 examples) are converted. A variety of functional groups are tolerated under the reaction conditions even though aldehydes and ketones are also reduced to the resp. alcs. under the reaction conditions. Mechanistic studies and control experiments were used to investigate the role of the Lewis acid in the reaction. Besides acting as the catalyst for the epoxide isomerization, the Lewis acid was found to facilitate the dehydrogenation of the hydrogen donor, which enhances the rate of the transfer hydrogenation step. These experiments addnl. indicate the direct transfer of hydrogen from the amine borane in the reduction step.

This literature about this compound(1086138-36-4)Formula: C44H69NP2has given us a lot of inspiration, and I hope that the research on this compound(Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine) can be further advanced. Maybe we can get more compounds in a similar way.

Reference:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

Safety of Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine, is researched, Molecular C44H69NP2, CAS is 1086138-36-4, about Catalytic Upgrading of Ethanol to n-Butanol via Manganese-Mediated Guerbet Reaction.

Replacement of precious metal catalysts in the Guerbet upgrade of ethanol to n-butanol with first-row metal complex catalysts is highly appreciated due to their economic and environmental friendliness. The manganese pincer complexes of the type [(RPNP)MnBr(CO)2] (R = iPr, Cy, tBu, Ph or Ad) are found to be excellent catalysts for upgrading ethanol to n-butanol. Under suitable reaction conditions and with an appropriate base, about 34% yield of n-butanol can be obtained in high selectivity. A detailed account on the effect of the temperature, solvent, nature, and proportion of base used and the stereoelectronic effects of the ligand substituents on the catalytic activity of the catalysts as well as the plausible deactivation pathways is presented.

This literature about this compound(1086138-36-4)Safety of Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)aminehas given us a lot of inspiration, and I hope that the research on this compound(Bis(2-(Di(adamantan-1-yl)phosphino)ethyl)amine) can be further advanced. Maybe we can get more compounds in a similar way.

Reference:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem