The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: Bis(norbornadiene)rhodium (I) tetrafluoroborate(SMILESS: [F-][B+3]([F-])([F-])[F-].C12=C3[Rh+]14567(C8=C5C9C6=C7C8C9)C%10=C4C2CC3%10,cas:36620-11-8) is researched.Related Products of 36620-11-8. The article 《Asymmetric total synthesis of C9′-epi-sinefungin》 in relation to this compound, is published in ChemRxiv. Let’s take a look at the latest research on this compound (cas:36620-11-8).
The natural nucleoside (+)-sinefungin, structurally similar to cofactor S-adenosyl-L-methionine (SAM), inhibits various SAM-dependent methyltransferases (MTs). Access to sinefungin analogs could serve as the basis for the rational design of small-mol. methyltransferase inhibitors. We developed a route to the unnatural C9′ epimer of sinefungin that employed a diastereoselective Overman rearrangement to install the key C6′ amino stereocenter. The ability for late stage modification is highlighted, opening an avenue for the discovery of new MTs inhibitors.
After consulting a lot of data, we found that this compound(36620-11-8)Related Products 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