Results 111 to 120 of about 13,233 (208)

??????????????? ??????????????? ??????????????? ???/???/??? ????????? ????????? ?????? ??????????????? ????????? ?????? [PDF]

open access: yes, 2018
Department of ChemistryRu-based sensitizers (N719, N3, black dye, etc.) have been developed continuously and reached an efficiency of ~11.7% under AM 1.5G irradiation (1000 W/m2).
Kim, Un-Young
core  

Optoelectronic properties of triphenylamine based dyes for solar cell applications. A DFT study [PDF]

open access: yes, 2018
Indexación: Scopus.GSM thanks to the Department of Chemistry at the Universidad Andres Bello, Concepcion, Chile. LHMH gratefully acknowledges financial support from CONACYT (Projects CB2015-257823) and to the Universidad Autónoma del Estado de Hidalgo ...
Alvarez-Romero, G.A.   +7 more
core   +1 more source

1-{[3-(Thiophen-2-yl)-4,5-dihydro-1,2-oxazol-5-yl]methyl}-2,3-dihydro-1H-indole-2,3-dione

open access: yesIUCrData, 2017
In the title compound, C16H12N2O3S, the indoline and thiophene rings are inclined to one another by 2.01 (2)°. The isoxazole ring adopts an envelope conformation, with the methine C atom as the flap, and its mean plane is inclined to the thiophene and ...
Ibtissam Rayni   +5 more
doaj   +1 more source

Synthesis of aza-rocaglates via ESIPT-mediated (3+2) photocycloaddition [PDF]

open access: yes, 2016
Synthesis of aza-rocaglates, nitrogen-containing analogues of the rocaglate natural products, is reported. The route features ESIPT-mediated (3+2) photocycloaddition of 1-alkyl-2-aryl-3-hydroxyquinolinones with the dipolarophile methyl cinnamate.
Cencic, Regina   +4 more
core   +1 more source

5′-Nitro-1,4-dihydrospiro[3,1-benzoxazine-2,3′-indolin]-2′-one

open access: yesIUCrData, 2018
In the title compound, C15H11N3O4, the six-membered oxazine ring adopts a half-chair conformation and is oriented at an angle of 78.63 (9)° with respect to the pyrrolidine ring of the indoline ring system, which adopts an envelope conformation. The spiro
Y. AaminaNaaz   +3 more
doaj   +1 more source

Highly Diastereo- and Enantioselective CuH-Catalyzed Synthesis of 2,3-Disubstituted Indolines [PDF]

open access: yes, 2015
A diastereo- and enantioselective CuH-catalyzed method for the preparation of highly functionalized indolines is reported. The mild reaction conditions and high degree of functional group compatibility as demonstrated with substrates bearing heterocycles,
Arp F. O.   +51 more
core   +4 more sources

Crystal structure of methyl 1-methyl-2-oxospiro[indoline-3,2′-oxirane]-3′-carboxylate

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2015
In the title compound, C12H11NO4, the dihedral angle between the indole ring system (r.m.s. deviation = 0.019 Å) and the oxirane ring is 88.8 (2)°. The oxirane O atom and the bridging ester O atom are in an approximate syn conformation [O—C—C—O = −25.4 ...
M. P. Savithri   +4 more
doaj   +1 more source

Concise Total Synthesis of (+)-Luteoalbusins A and B [PDF]

open access: yes, 2015
The first total synthesis of (+)-luteoalbusins A and B is described. Highly regio- and diastereoselective chemical transformations in our syntheses include a Friedel–Crafts C3-indole addition to a cyclotryptophan-derived diketopiperazine, a late-stage ...
Adams, Timothy Cho   +3 more
core   +1 more source

New Photochromic Salt Spiropyrans of Indoline Series

open access: yesDoklady Chemistry, 2019
The synthesis and study of the structure and photochromic properties of the new salt spiropyrans of the indoline series containing chlorine and bromine atoms as a substituent at the 6' position in 2H-chromene moiety are presented. The structure of the obtained compounds was confirmed by NMR 1H spectroscopy and X-ray diffraction analysis.
A. D. Pugachev   +9 more
openaire   +2 more sources

Direct, enantioselective synthesis of pyrroloindolines and indolines from simple indole derivatives [PDF]

open access: yes, 2013
The (R)-BINOL·SnCl_4-catalyzed formal (3+2) cycloaddition between 3-substituted indoles and benzyl 2-trifluoroacetamidoacrylate is a direct, enantioselective method to prepare pyrroloindolines from simple starting materials. However, under the originally
Reisman, Sarah E., Wang, Jane Ni Haoxuan
core   +1 more source

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