861909-35-5

Usage

Uses

Used in Materials Science:
(11bR)-2,6-Bis([1,1'-biphenyl]-4-yl)-8,9,10,11,12,13,14,15-octahydro-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin is used as a component in the development of new materials due to its complex structure and potential for interaction with other molecules.
Used in Organic Synthesis:
(11bR)-2,6-Bis([1,1'-biphenyl]-4-yl)-8,9,10,11,12,13,14,15-octahydro-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin serves as a building block or intermediate in the synthesis of other complex organic molecules, taking advantage of its reactive hydroxy group and the presence of a phosphorus atom.
Used in Pharmaceutical Research:
(11bR)-2,6-Bis([1,1'-biphenyl]-4-yl)-8,9,10,11,12,13,14,15-octahydro-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin is used as a starting material or modifier in the design and synthesis of new pharmaceutical agents, potentially targeting various therapeutic areas.
Used in Chemical Reactivity Studies:
(11bR)-2,6-Bis([1,1'-biphenyl]-4-yl)-8,9,10,11,12,13,14,15-octahydro-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin is utilized in research to understand its reactivity with other functional groups, which can provide insights into new reaction pathways and the development of novel chemical processes.

Upstream product

• 2757287-34-4 (R)-3,3'-bis-biphenyl-4-yl-5,6,7,8,5',6',7',8'-octahydro-[1,1']binaphthalenyl-2,2'-diol 

Relevant academic research and scientific papers

Highly Enantioselective Allylic C-H Alkylation of Terminal Olefins with Pyrazol-5-ones Enabled by Cooperative Catalysis of Palladium Complex and Br?nsted Acid

A highly enantioselective allylic C-H alkylation reaction of allylarenes with pyrazol-5-ones has been established by the cooperative catalysis of a chiral palladium complex and chiral Br?nsted acid to afford a wide spectrum of functionalized chiral N-hete