Some scientific research about 1214711-48-4

In some applications, this compound(1214711-48-4)Related Products of 1214711-48-4 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Related Products of 1214711-48-4. 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: (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, is researched, Molecular C18H13BCl3F4N3O, CAS is 1214711-48-4, about N-Heterocyclic carbene-catalyzed desymmetrization of functionalized 1,4-dienes via Stetter Reaction.

The asym. desymmetrization of 1,4-dienes via chiral N-heterocyclic carbene catalyzed Stetter-type umpolung reaction was demonstrated. A variety of differently substituted dienes were tolerated very well, affording cyclic ketones with two consecutive stereogenic centers (including one quaternary carbon) in moderate to high yields and with high to excellent enantioselectivities. This work expanded both reaction types of catalytic diene desymmetrizations and substrate diversity in NHC catalyzed desym. transformations.

In some applications, this compound(1214711-48-4)Related Products of 1214711-48-4 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Quinuclidine – Wikipedia,
Quinuclidine | C7H13N | ChemSpider