In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Silver-Assisted, Iridium-Catalyzed Allylation of Bis[(pinacolato)boryl]methane Allows the Synthesis of Enantioenriched Homoallylic Organoboronic Esters, published in 2016-05-06, which mentions a compound: 1265884-98-7, mainly applied to silver assisted iridium catalyzed allylation pinacolatoborylmethane allyl carbonate; homoallylic organoboronic ester chiral preparation; crystal structure chiral homoallylic indolinylboronic ester; mol structure chiral homoallylic indolinylboronic ester, Related Products of 1265884-98-7.
Described here is an enantioselective approach of making chiral, β-substituted homoallylic organoboronic esters. In the presence of LiOtBu and a catalytic amount of Ag salt, com. bis[(pinacolato)boryl]methane participated in the Ir-catalyzed asym. allylation reactions, delivered a CH2B(pin) group, and yielded the title compounds from allylic carbonates. The synthetic utility of the prepared chiral organoboronates was demonstrated by their conversion to other important classes of compounds
Here is just a brief introduction to this compound(1265884-98-7)Related Products of 1265884-98-7, more information about the compound(5-(11bR)-Dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-yl-5H-dibenz[b,f]azepine) is in the article, you can click the link below.
Reference:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem