Category: 2160535-56-6

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After consulting a lot of data, we found that this compound(2160535-56-6)Recommanded Product: 2160535-56-6 can be used in many types of reactions. And in most cases, this compound has more advantages.

Recommanded Product: 2160535-56-6. 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)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide, is researched, Molecular C39H40NO3PS, CAS is 2160535-56-6, about Gold-Catalyzed Asymmetric Intramolecular Cyclization of N-Allenamides for the Synthesis of Chiral Tetrahydrocarbolines. Author is Wang, Yidong; Zhang, Peichao; Di, Xiaoyu; Dai, Qiang; Zhang, Zhan-Ming; Zhang, Junliang.

Highly enantioselective gold-catalyzed intramol. cyclization of N-allenamides was implemented by utilizing a designed chiral sulfinamide phosphine ligand (PC-Phos) [e.g., allenamide I → tetrahydrocarboline II (99%, 96% ee) in presence of Me2S.AuCl, AgNTf2 and ligand III in CH2Cl2 at -50°]. This represents the first example of highly enantioselective intramol. cyclization of N-allenamides. The practicality of this reaction was validated in the total synthesis of (R)-desbromoarborescidine A and formal synthesis of (R)-desbromoarborescidine C and (R)-deplancheine. Moreover, the catalyst system PC-Phos/AuNTf2 proved to be specifically efficient to promote the desymmetrization of N-allenamides in excellent yields with satisfactory ee values.

After consulting a lot of data, we found that this compound(2160535-56-6)Recommanded Product: 2160535-56-6 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Decrypt The Mystery Of 2160535-56-6

Compounds in my other articles are similar to this one((R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide)Category: benzodioxans, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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: 2160535-56-6, is researched, SMILESS is CC([S@](N[C@@H](C1=CC=CC(C2(C)C)=C1OC3=C2C=CC=C3P(C4=CC=CC=C4)C5=CC=CC=C5)C6=CC=C(OC)C=C6)=O)(C)C, Molecular C39H40NO3PSJournal, Article, Research Support, Non-U.S. Gov’t, Angewandte Chemie, International Edition called Gold-Catalyzed Asymmetric Intramolecular Cyclization of N-Allenamides for the Synthesis of Chiral Tetrahydrocarbolines, Author is Wang, Yidong; Zhang, Peichao; Di, Xiaoyu; Dai, Qiang; Zhang, Zhan-Ming; Zhang, Junliang, the main research direction is gold catalyzed asym intramol cyclization allenamide chiral hydrocarboline synthesis; chiral sulfinamide phosphine ligand gold catalyzed asym intramol cyclization; desbromoarborescidine A synthesis desbromoarborescidine C formal synthesis; deplancheine formal synthesis; desymmetrization allenamide; allenamides; cyclization; enantioselectivity; gold; tetrahydrocarboline.Category: benzodioxans.

Highly enantioselective gold-catalyzed intramol. cyclization of N-allenamides was implemented by utilizing a designed chiral sulfinamide phosphine ligand (PC-Phos) [e.g., allenamide I → tetrahydrocarboline II (99%, 96% ee) in presence of Me2S.AuCl, AgNTf2 and ligand III in CH2Cl2 at -50°]. This represents the first example of highly enantioselective intramol. cyclization of N-allenamides. The practicality of this reaction was validated in the total synthesis of (R)-desbromoarborescidine A and formal synthesis of (R)-desbromoarborescidine C and (R)-deplancheine. Moreover, the catalyst system PC-Phos/AuNTf2 proved to be specifically efficient to promote the desymmetrization of N-allenamides in excellent yields with satisfactory ee values.

Compounds in my other articles are similar to this one((R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide)Category: benzodioxans, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

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Compounds in my other articles are similar to this one((R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide)HPLC of Formula: 2160535-56-6, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide( cas:2160535-56-6 ) is researched.HPLC of Formula: 2160535-56-6.Wang, Yidong; Zhang, Peichao; Di, Xiaoyu; Dai, Qiang; Zhang, Zhan-Ming; Zhang, Junliang published the article 《Gold-Catalyzed Asymmetric Intramolecular Cyclization of N-Allenamides for the Synthesis of Chiral Tetrahydrocarbolines》 about this compound( cas:2160535-56-6 ) in Angewandte Chemie, International Edition. Keywords: gold catalyzed asym intramol cyclization allenamide chiral hydrocarboline synthesis; chiral sulfinamide phosphine ligand gold catalyzed asym intramol cyclization; desbromoarborescidine A synthesis desbromoarborescidine C formal synthesis; deplancheine formal synthesis; desymmetrization allenamide; allenamides; cyclization; enantioselectivity; gold; tetrahydrocarboline. Let’s learn more about this compound (cas:2160535-56-6).

Highly enantioselective gold-catalyzed intramol. cyclization of N-allenamides was implemented by utilizing a designed chiral sulfinamide phosphine ligand (PC-Phos) [e.g., allenamide I → tetrahydrocarboline II (99%, 96% ee) in presence of Me2S.AuCl, AgNTf2 and ligand III in CH2Cl2 at -50°]. This represents the first example of highly enantioselective intramol. cyclization of N-allenamides. The practicality of this reaction was validated in the total synthesis of (R)-desbromoarborescidine A and formal synthesis of (R)-desbromoarborescidine C and (R)-deplancheine. Moreover, the catalyst system PC-Phos/AuNTf2 proved to be specifically efficient to promote the desymmetrization of N-allenamides in excellent yields with satisfactory ee values.

Compounds in my other articles are similar to this one((R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide)HPLC of Formula: 2160535-56-6, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

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Wang, Yidong; Zhang, Peichao; Di, Xiaoyu; Dai, Qiang; Zhang, Zhan-Ming; Zhang, Junliang published the article 《Gold-Catalyzed Asymmetric Intramolecular Cyclization of N-Allenamides for the Synthesis of Chiral Tetrahydrocarbolines》. Keywords: gold catalyzed asym intramol cyclization allenamide chiral hydrocarboline synthesis; chiral sulfinamide phosphine ligand gold catalyzed asym intramol cyclization; desbromoarborescidine A synthesis desbromoarborescidine C formal synthesis; deplancheine formal synthesis; desymmetrization allenamide; allenamides; cyclization; enantioselectivity; gold; tetrahydrocarboline.They researched the compound: (R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide( cas:2160535-56-6 ).Application In Synthesis of (R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide. 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:2160535-56-6) here.

Highly enantioselective gold-catalyzed intramol. cyclization of N-allenamides was implemented by utilizing a designed chiral sulfinamide phosphine ligand (PC-Phos) [e.g., allenamide I → tetrahydrocarboline II (99%, 96% ee) in presence of Me2S.AuCl, AgNTf2 and ligand III in CH2Cl2 at -50°]. This represents the first example of highly enantioselective intramol. cyclization of N-allenamides. The practicality of this reaction was validated in the total synthesis of (R)-desbromoarborescidine A and formal synthesis of (R)-desbromoarborescidine C and (R)-deplancheine. Moreover, the catalyst system PC-Phos/AuNTf2 proved to be specifically efficient to promote the desymmetrization of N-allenamides in excellent yields with satisfactory ee values.

There are many compounds similar to this compound(2160535-56-6)Application In Synthesis of (R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide. if you want to know more, you can check out my other articles. I hope it will help you，maybe you’ll find some useful information.

Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

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From this literature《Gold-Catalyzed Asymmetric Intramolecular Cyclization of N-Allenamides for the Synthesis of Chiral Tetrahydrocarbolines》,we know some information about this compound(2160535-56-6)Safety of (R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide, but this is not all information, there are many literatures related to this compound(2160535-56-6).

Safety of (R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: (R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide, is researched, Molecular C39H40NO3PS, CAS is 2160535-56-6, about Gold-Catalyzed Asymmetric Intramolecular Cyclization of N-Allenamides for the Synthesis of Chiral Tetrahydrocarbolines. Author is Wang, Yidong; Zhang, Peichao; Di, Xiaoyu; Dai, Qiang; Zhang, Zhan-Ming; Zhang, Junliang.

Highly enantioselective gold-catalyzed intramol. cyclization of N-allenamides was implemented by utilizing a designed chiral sulfinamide phosphine ligand (PC-Phos) [e.g., allenamide I → tetrahydrocarboline II (99%, 96% ee) in presence of Me2S.AuCl, AgNTf2 and ligand III in CH2Cl2 at -50°]. This represents the first example of highly enantioselective intramol. cyclization of N-allenamides. The practicality of this reaction was validated in the total synthesis of (R)-desbromoarborescidine A and formal synthesis of (R)-desbromoarborescidine C and (R)-deplancheine. Moreover, the catalyst system PC-Phos/AuNTf2 proved to be specifically efficient to promote the desymmetrization of N-allenamides in excellent yields with satisfactory ee values.

From this literature《Gold-Catalyzed Asymmetric Intramolecular Cyclization of N-Allenamides for the Synthesis of Chiral Tetrahydrocarbolines》,we know some information about this compound(2160535-56-6)Safety of (R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide, but this is not all information, there are many literatures related to this compound(2160535-56-6).

Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem