نتایج جستجو برای: indoline

تعداد نتایج: 604  

Journal: :Molecules 2013
Zhaoyang Liu Haruhiko Ojima Ziruo Hong Junji Kido Wenjing Tian Xiao-Feng Wang

A donor-acceptor (D-A) type indoline dye, D149, was used as an electron donor in solution-processed organic solar cells (OSCs). For bulk-heterojunction (BHJ) type OSCs with PC70BM as electron acceptor, the power conversion efficiency (PCE) is sensitive to the amount of D149 in the D149/PC70BM blend film. When the concentration of D149 in the blend film was as low as 5%, the highest PCE of up to...

2011
Hua-quan Liu Dong-mei Fan De-cai Wang Ping-Kai Ou-yang

In the title compound, C(15)H(10)ClNO(2),the dihedral angle between the mean planes of the benzene and 6-chloro-indoline-2,3-dione ring systems, linked through a methyl-ene group, is 81.68 (10)°. In the crystal, mol-ecules are connected by C-H⋯O hydrogen bonds, generating C(6) chains propagating in [010].

Journal: :Chemical communications 2015
Minqiang Jia Magda Monari Qing-Qing Yang Marco Bandini

The highly enantioselective synthesis of densely functionalized 2,3-indoline-cyclobutanes by means of chiral gold catalysis is presented. Intermolecular formal [2+2]-cycloaddition reactions between substituted indoles and allenamides enabled direct access to methylenecyclobutane-fused indolines, featuring two consecutive quaternary stereogenic centers with excellent stereochemical control (dr >...

2013
Mitsuhiro Ueda Yoshitaka Uenoyama Nozomi Terasoma Shoko Doi Shoji Kobayashi Ilhyong Ryu John A Murphy

A straightforward synthesis of 4,4-spirocyclic indol γ-lactams by tandem radical cyclization of iodoaryl allyl azides with CO was achieved. The reaction of iodoaryl allyl azides, TTMSS and AIBN under CO pressure (80 atm) in THF at 80 °C gave the desired 4,4-spirocyclic indoline, benzofuran, and oxindole γ-lactams in moderate to good yields.

Journal: :Phytochemistry 1995
J G Dong W Bornmann K Nakanishi N Berova

SCF-CI-dipole velocity MO calculations have shown that the bisignate circular dichroic curves of vinblastine/vincristine alkaloids at ca 210 and 220-230 nm are due to exciton coupling between the indoline and indole moieties. Furthermore, a combination of X-ray crystal structure data with MM2 local energy minimization provides a convenient means for estimation of the preferred solution conforma...

2011
Qi Wang Yue-Jun Zhang Mao-Sen Yuan Jun-Ru Wang

In the title mol-ecule, C(16)H(13)NO, the indoline-2-one ring system is nearly planar [maximum atomic deviation = 0.082 (2) Å] and is oriented at a dihedral angle of 66.60 (12)° with respect to the phenyl ring. In the crystal, inter-molecular N-H⋯O hydrogen bonds link the mol-ecules into supra-molecular dimers.

Journal: :Optics and Spectroscopy 2022

The methods of absorption electronic and NMR spectroscopy were used to study the processes complexation during interaction molecules unsubstituted indoline spiropyran with aluminum salts. mechanism formation structure complexes two types has been established. Negative photochromism complex merocyanine form ions was found. stability metal action various agents investigated. Keywords: photochromi...

Journal: :Chemical communications 2016
Xu Zhu Shunsuke Chiba

Lewis acid-mediated conjugate addition of vinyl azides to electron-deficient alkenes led to the efficient construction of 1-pyrroline skeletons. The reactions of vinyl azides with 3-alkylidene-2-oxoindolines afford 3',4'-dihydrospiro[indoline-3,2'-pyrrol]-2-ones in a diastereoselective fashion, whereas those with dimethyl 2-alkylidenemalonates provide 4,5-dihydro-3H-pyrroles.

2014
Chao Wang Yan-Hong Jiang Chao-Guo Yan

The one-pot four-component reaction of benzohydrazide (2-picolinohydrazide), acetylenedicarboxylate, isatins and malononitrile (ethyl cyanoacetate) with triethylamine as base catalyst afforded functionalized 1-benzamidospiro[indoline-3,4'-pyridines] in good yields. (1)H NMR spectra indicated that an equilibrium of cis/trans-conformations exist in the obtained products.

Journal: :Journal of the American Chemical Society 2005
Liming Zhang

The treatment of readily available propargylic indole-3-acetates with a catalytic amount of AuCl(PPh3)/AgSbF6 leads to tandem activations of the propargylic esters and the in situ generated allenylic esters, resulting in expeditious access to highly functionalized cyclobutanes with fused 2,3-indoline and gamma-lactone rings and an exocyclic E-double bond through sequential 3,3-rearrangement and...

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