Can You Really Do Chemisty Experiments About 36620-11-8

After consulting a lot of data, we found that this compound(36620-11-8)Application of 36620-11-8 can be used in many types of reactions. And in most cases, this compound has more advantages.

Application of 36620-11-8. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: Bis(norbornadiene)rhodium (I) tetrafluoroborate, is researched, Molecular C14H8BF4Rh, CAS is 36620-11-8, about Efficient synthesis of chiral 2,3-dihydro-benzo[b]thiophene 1,1-dioxides via Rh-catalyzed hydrogenation. Author is Liu, Gongyi; Zhang, Heng; Huang, Yi; Han, Zhengyu; Liu, Gang; Liu, Yuanhua; Dong, Xiu-Qin; Zhang, Xumu.

Rh-catalyzed asym. hydrogenation of prochiral substituted benzo[b]thiophene 1,1-dioxides was successfully developed, affording various chiral 2,3-dihydrobenzo[b]thiophene 1,1-dioxides I (R = H, 6-MeO; R1 = C6H5, 4-MeOC6H4, 4-FC6H4, etc.; R2 = C6H5, 4-MeOC6H4, 3-H3CC6H4, etc.) with high yields and excellent enantioselectivities (up to 99% yield and >99% ee). In particular, for challenging substrates, such as aryl substituted substrates with sterically hindered groups and alkyl substituted substrates, the reaction proceeded smoothly in catalytic system with excellent results. The gram-scale asym. hydrogenation proceeded well with 99% yield and 99% ee in the presence of 0.02 mol% (S/C = 5000) catalyst loading. The possible hydrogen-bonding interaction between the substrate and the ligand may play an important role in achieving high reactivity and excellent enantioselectivity.

After consulting a lot of data, we found that this compound(36620-11-8)Application of 36620-11-8 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Quinuclidine – Wikipedia,
Quinuclidine | C7H13N | ChemSpider