160257-85-2Relevant articles and documents
Highly ordered columnar superlattice nanostructures with improved charge carrier mobility by thermotropic self-assembly of triphenylene-based discotics
Bi, Jingze,Wu, Hao,Zhang, Zhenhu,Zhang, Ao,Yang, Huanzhi,Feng, Yuwen,Fang, Yi,Zhang, Lina,Wang, Zhengran,Qu, Wentao,Liu, Feng,Zhang, Chunxiu
supporting information, p. 12463 - 12469 (2019/10/28)
A series of triphenylene esters with two ester groups at 2,3-, 2,7-, 2,6- and 3,6- substituent positions was successfully synthesized and fully investigated. Their self-assembly properties were exhaustively examined by DSC, POM, 1DXRD, 2DXRD, SAXS, TEM methods together with EDM and ESP calculations. It was unexpected that the 3,6-substituted triphenylene ester T5E36 formed an uncommonly helical hexagonal columnar superlattice structure made up of 91 right-handed helixes with a pitch of 60.3 ?. This helical superlattice structure was further studied by using transmission electron microscopy and the diameter of the T5E36 particles was found to be at the nanometer scale. Ultimately, the bipolar charge carrier mobility was measured by the time-of-flight method to be in the order of 10-1 cm2 V-1 s-1. The formation of this helical superlattice nanostructure no doubt improved their electronic properties and made them more attractive in organic electronics.
Negishi cross-coupling reaction as a route to isocombretastatins
Malysheva, Yulia B.,Buchvalova, Svetlana Y.,Svirshchevskaya, Elena V.,Fokin, Valery V.,Fedorov, Alexey Y.
supporting information, p. 1772 - 1776 (2013/09/12)
A series of isocombretastatins A has been synthesized by a new method based on the Negishi cross-coupling reaction in 19-84% yields. Five of the synthesized compounds exhibit high cytotoxic activity in nanomolar concentrations (IC50 = 1-100 n) towards Jurkat, K562, Colo357, and A549 cell lines. Georg Thieme Verlag Stuttgart · New York.
Total synthesis of "Aliskiren": The first renin inhibitor in clinical practice for hypertension
Hanessian, Stephen,Guesne, Sebastien,Chenard, Etienne
supporting information; scheme or table, p. 1816 - 1819 (2010/09/16)
We report a "macrocycle route" toward aliskiren, a drug presently marketed for the treatment of hypertension, using a highly stereocontrolled approach starting from a common "isopropyl chiron". Highlights of the synthesis include a challenging RCM reaction to produce a nine-membered unsaturated lactone, a highly stereoselective catalytic Du Bois aziridination, and a regio- and diastereoselective aziridine ring-opening to a vicinal amino alcohol.
