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: 36620-11-8, is researched, SMILESS is [F-][B+3]([F-])([F-])[F-].C12=C3[Rh+]14567(C8=C5C9C6=C7C8C9)C%10=C4C2CC3%10, Molecular C14H8BF4RhJournal, Article, Research Support, Non-U.S. Gov’t, Organic Letters called Highly Regio- and Enantioselective Hydrogenation of Conjugated α-Substituted Dienoic Acids, Author is Liu, Xian; Liu, Song; Wang, Quanjun; Zhou, Gang; Yao, Lin; Ouyang, Qin; Jiang, Ru; Lan, Yu; Chen, Weiping, the main research direction is unsaturated acid enantioselective synthesis hydrogenation Trifer catalyst complex; enantioselective hydrogenation conjugated dienoic acid Trifer catalyst complex.Electric Literature of C14H8BF4Rh.
Highly regio- and enantioselective hydrogenation of conjugated α-substituted dienoic acids was realized for the first time using Trifer-Rh complex, providing a straightforward method for the synthesis of chiral α-substituted γ,δ-unsaturated acids. DFT calculations revealed N+H-O hydrogen bonding interaction is formed to stabilize the transition state and the coordination of 4,5-double bond to Rh(III) center would facilitate the reductive elimination process. This hydrogenation provided a gram-scale synthesis of the precursor of sacubitril.
In some applications, this compound(36620-11-8)Electric Literature of C14H8BF4Rh 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