Search results for "Side product"
showing 8 items of 8 documents
A Light-Induced Vinylogous Nazarov-Type Cyclization
2016
The first examples of a photochemically induced vinylogous Nazarov-type cyclization forming a cycloheptadienone core are described. The reaction can be included in a three-step cascade consisting of a photochemical isoxazole-azirine ring contraction, cobalt(II)-catalyzed ring expansion, and the photochemical cyclization. Furthermore, the first representative of the hitherto unknown 1-azatricyclo[2.2.0.0(2,6)]hexanes has been identified as a side product of the azirine formation.
3,4-Bis(4-fluorophenyl)-1,2,5-oxadiazole 2-oxide
2006
The title compound, C14H8F2N2O2, also known as di(4-F-phenyl)furazan N-oxide, was found as a side product in the synthesis of isoxazole derivatives. The are two molecules in the asymmetric unit. The bond length of the dipolar N—O unit is 1.107 (7) A. X-ray analysis confirmed the compound to have the desired structure
Ethyl (2,3-dihydro-1H,1′H-2,3′-biindol-1-yl)glyoxylate
2007
The crystal structure of the title compound, C20H18N2O3, was determined in the course of our studies of the synthesis of 3-acylindole derivatives. We obtained it as an unexpected racemic side product. The crystal structure contains chains of dimers along the a axis.
Die spektroskopische untersuchung einer cyclischen, tetrameren verbindung aus p-kresol und formaldehyd
1972
In Anlehnung an den Syntheseweg von HAYES und HUNTER wurde eine cyclische, tetramere Verbindung (VII) uber eine linear 4-Kernverbindung (VI) (aus p-Kresol und Formaldehyd) hergestellt. Ihre Struktur wurde spektroskopisch untersucht. Mittels UV- und IR-Spektren last sich VII von der Ausgangsstufe VI und einem Konkurrenzprodukt VIII unterscheiden. Die H-NMR-Spektren der Ringverbindung und ihrer Ausgangsverbindung (VI) stimmen vollstandig mit den angegebenen Strukturformeln uberein; sie geben, bei 20 und 60°C aufgenommen, Hinweise auf bestimmte Konformere der Ringverbindung. Das massenspektrometrisch bestimmte Molekulargewicht (480) stimmt mit dem berechneten (480,6) uberein. Following the syn…
Ir-Catalyzed Cycloaddition of Tribenzocyclyne with Biphenylenes
2021
We demonstrate that Ir-catalyzed C-C bond activation in biphenylenes followed by a reaction with tribenzocyclyne is a suitable method for synthesizing strained and unknown monoadducts with the tetradehydrotetrabenzo[a,c,e,i]cyclododecene scaffold ([12]annulenes). Modification of reaction conditions also furnished [12]annulene products with cis and/or trans double bonds formed by hydrogen transfer. The [9]annulene side product was formed upon the reaction of the benzyl radical with tribenzocyclyne during the Bergman cyclization. All isolated compounds were fully characterized by HRMS, NMR, and X-ray diffraction analysis.
N-{(Z)-2-[1-(Triisopropylsilyl)-1H-indol-3-yl]-2-(triisopropylsilyloxy)vinyl}-2-(3,4,5-trimethoxyphenyl)acetamide
2007
The molecular structure of the title compound, C39H62N2O5Si2, obtained as an unexpected side product, was determined in the course of our studies on the synthesis of N-triisopropyl-1H-indol-3-yl derivatives. Interestingly, although the triisopropylsilyl group was intended as a temporary protecting group, the compound comprises a remarkably stable N—Si bond. The vinyl C=C double bond possesses a Z configuration.
ChemInform Abstract: Selective Ipso-Nitration of tert-Butylcalix(4)arene 1,3-Diethers: X- Ray Structure of an Unexpected Side Product.
2010
3-Ethylindan-1-one
2017
The title compound, C11H12O, has been prepared as a side product in the attempted room-temperature synthesis of (E)-1-phenylpent-2-en-1-one. The molecular structure consists of an approximately planar indanone core (r.m.s. deviation = 0.042 Å) with the ethyl group protruding from this plane. In the crystal, centrosymmetrically related molecules are linked into dimers by pairs of C—H...O hydrogen bonds, forming rings ofR22(10) graph-set motif. The dimers are further connected by C—H...π interactions into chains running parallel to [-101].