Some scientific research tips on 1214711-48-4

I hope my short article helps more people learn about this compound((5aS,10bR)-2-(2,4,6-Trichlorophenyl)-4,5a,6,10b-tetrahydro-2H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-11-ium tetrafluoroborate)Quality Control of (5aS,10bR)-2-(2,4,6-Trichlorophenyl)-4,5a,6,10b-tetrahydro-2H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-11-ium tetrafluoroborate. Apart from the compound(1214711-48-4), you can read my other articles to know other related compounds.

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.Zhao, Zhifei; Yang, Shuang; Lan, Shouang; Liu, Jinggong; Liu, Shuhua; Fang, Xinqiang researched the compound: (5aS,10bR)-2-(2,4,6-Trichlorophenyl)-4,5a,6,10b-tetrahydro-2H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-11-ium tetrafluoroborate( cas:1214711-48-4 ).Quality Control of (5aS,10bR)-2-(2,4,6-Trichlorophenyl)-4,5a,6,10b-tetrahydro-2H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-11-ium tetrafluoroborate.They published the article 《Asymmetric Synthesis of Dihydronaphthalene-1,4-diones via Carbene-Catalyzed Stereodivergent Reaction》 about this compound( cas:1214711-48-4 ) in Advanced Synthesis & Catalysis. Keywords: dihydronaphthalenedione enantioselective preparation; formylaryl diketone preparation enantioselective benzoin cyclization carbene catalyst. We’ll tell you more about this compound (cas:1214711-48-4).

2-Hydroxy-2,3-dihydronaphthalene-1,4-diones (HDNDs) are ubiquitous in natural products and bioactive mols., but the rapid asym. construction of such scaffolds remains a significant challenge to date. Reported herein is the rapid construction of the above key units via carbene-catalyzed benzoin reaction. The resolution technique of divergent reaction on racemic mixture (divergent RRM) was employed, affording both isomers of HDNDs in a one-step fashion. Disubstituted substrates afford products with two contiguous quaternary stereocenters. A series of highly selective transformations on the products can be realized, and mechanistic studies indicate that the benzoin reaction is much faster than the racemization process and the aldol reaction.

I hope my short article helps more people learn about this compound((5aS,10bR)-2-(2,4,6-Trichlorophenyl)-4,5a,6,10b-tetrahydro-2H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-11-ium tetrafluoroborate)Quality Control of (5aS,10bR)-2-(2,4,6-Trichlorophenyl)-4,5a,6,10b-tetrahydro-2H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-11-ium tetrafluoroborate. Apart from the compound(1214711-48-4), you can read my other articles to know other related compounds.

Reference:
Quinuclidine – Wikipedia,
Quinuclidine | C7H13N | ChemSpider