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