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: 1214711-48-4, is researched, SMILESS is ClC1=C(N2N=C3[N+]([C@@]4([H])[C@@](CC5=C4C=CC=C5)([H])OC3)=C2)C(Cl)=CC(Cl)=C1.F[B-](F)(F)F, Molecular C18H13BCl3F4N3OJournal, Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov’t, Journal of the American Chemical Society called N-Heterocyclic Carbene Catalyzed Asymmetric Hydration: Direct Synthesis of α-Protio and α-Deuterio α-Chloro and α-Fluoro Carboxylic Acids, Author is Vora, Harit U.; Rovis, Tomislav, the main research direction is heterocyclic carbene catalyzed asym hydration chloro aldehyde halo enal; enantioselective synthesis chloro fluoro deuterio carboxylic acid.Category: quinuclidine.
Asym. hydration of α,α-dichloro aldehydes and α-halo enals via a NHC-catalyzed redox process to yield enantioenriched α-chloro and α-fluoro carboxylic acids is described herein. The developed reaction allows for installation of an α-deuterium to give rise to enantioenriched α-deutero α-halo acids using D2O as the deuteron source.
Compounds in my other articles are similar to this one((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)Category: quinuclidine, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.
Reference:
Quinuclidine – Wikipedia,
Quinuclidine | C7H13N | ChemSpider