35945-68-7Relevant academic research and scientific papers
Syntheses of perillene and natural congeners via Li2CuCl4-catalyzed cross-coupling reaction of allylic carbonates
Sun, Ya-Nan,Wang, Qi,He, Ling,Wang, Xi,Li, Wei-Dong Z.
supporting information, (2022/01/24)
Perillene is an essential ingredient in a Chinese patent drug and features some fascinating biological activities. We present herein an efficient pathway to perillene that hangs on the cross-coupling reaction of allylic carbonates with furfuryl Grignard r
Monomer-on-monomer (MoM) Mitsunobu reaction: Facile purification utilizing surface-initiated sequestration
Maity, Pradip K.,Rolfe, Alan,Samarakoon, Thiwanka B.,Faisal, Saqib,Kurtz, Ryan D.,Long, Toby R.,Schaetz, Alexander,Flynn, Daniel L.,Grass, Robert N.,Stark, Wendelin J.,Reiser, Oliver,Hanson, Paul R.
supporting information; experimental part, p. 8 - 10 (2011/02/27)
A monomer-on-monomer (MoM) Mitsunobu reaction utilizing norbornenyl-tagged (Nb-tagged) reagents is reported, whereby purification was rapidly achieved by employing ring-opening metathesis polymerization, which was initiated by any of three methods utilizi
45. Synthesis of (all-E,2R,2′R)-oscillol
Traber, Bruno,Pfander, Hanspeter
, p. 499 - 506 (2007/10/03)
Optically active (all-E,2R,2′R)-oscillol (=(all-E,2R,2′R)-3,4,3′,4′-tetradehydro-1,2,1′,2′- tetrahydro-ψ,ψ-carotene-1,2,1′,2′-tetrol; 1) was synthesized according to the C10 + C20 + C10 = C40 strategy, applying
