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Abstract E-Urocanic acid exhibits a single, featureless, long-wavelength absorption band with λmax˜258 nm in water. However, the quantum efficiency for E→Z photoisomerization is wavelength dependent in this region, with the maximum value at the low energy edge of the band (e.g. 313 nm) and appreciably lower efficiencies measured at ≦ 300 nm. 相似文献
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Alexander M. Moiseenkov Evgeni V. Polunin Alexei V. Semenovsky 《Tetrahedron letters》1981,22(34):3309-3312
Nine-step synthesis of the title triterpenol from (E,E)-farnesol using a two-stage cis-C5-homologation procedure is descrilaed. 相似文献
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The geometry of the ground states of the isomers and transition state for the systems HCN ? HNC and BCN ? BNC have been investigated using a wide variety of basis sets, both at the self-consistent-field (SCF ) level and including correlation at the second-, and third-order Møller–Plesset (MP 2 and MP 3) levels. The barrier to isomerization and the isomerization energy were shown to be strongly dependent on the basis set and method, particularly for the BCN system. 相似文献
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Lieby Zborovsky Arseni Kostenko Dmitry Bravo‐Zhivotovskii Yitzhak Apeloig 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(41):14666-14670
The E and Z geometric isomers of a stable silene (tBu2MeSi)(tBuMe2Si)Si=CH(1‐Ad) ( 1 ) were synthesized and characterized spectroscopically. The thermal Z to E isomerization of 1 was studied both experimentally and computationally using DFT methods. The measured activation parameters for the 1Z ? 1E isomerization are: Ea=24.4 kcal mol?1, ΔH≠=23.7 kcal mol?1, ΔS≠=?13.2 e.u. Based on comparison of the experimental and DFT calculated (at BP86‐D3BJ/def2‐TZVP(‐f)//BP86‐D3BJ/def2‐TZVP(‐f)) activation parameters, the Z?E isomerization of 1 proceeds through an unusual (unprecedented for alkenes) migration–rotation–migration mechanism (via a silylene intermediate), rather than through the classic rotation mechanism common for alkenes. 相似文献
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Rakesh Kumar Gueijun Ji Leonard I. Wiebe Edward E. Knaus 《Journal of heterocyclic chemistry》1991,28(3):711-715
5-Iodo-3′-O-(1-methyl-1,4-dihydropyridyl-3-carbonyl)-2′-deoxyuridine (15a) , 5-vinyl-3′-O-(1-methyl-1,4-di-hydropyridyl-3-carbonyl)-2′-deoxyuridine (15b) and (E)-5-(2-iodovinyl)-3′-O-(1-methyl-1,4-dihydropyridyl-3-carbonyl)-2′-deoxyuridine (15c) were synthesized for future evaluation as lipophilic brain-selective antiviral agents for the treatment of herpes simplex encephalitis. Quaternization of the 3′-O-(3-pyridylcarbonyl) compounds 10–11 using iodomethane afforded the corresponding 1-methylpyridinium salts 12–13 which were reduced with sodium dithionite to yield the corresponding 3′-O-(1-methyl-1,4-dihydropyridyl-3-carbonyl) compounds 14–15. 相似文献
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Saito H Sivaguru J Jockusch S Inoue Y Adam W Turro NJ 《Chemical communications (Cambridge, England)》2005,(27):3424-3426
Oxazolidinone-functionalized enecarbamates undergo diastereoselective E/Z photoisomerization upon direct and triplet sensitized irradiations with chiral/achiral sensitizers, showing that the enhanced product diastereoselectivity depends on the solvent and temperature. 相似文献
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Gottfried Mrkl Thomas Knott Peter Kreitmeier Thomas Burgemeister Fritz Kastner 《Helvetica chimica acta》2000,83(3):592-602
Diepoxy[18]annulenes(10.0): ( Z , E , Z , E , Z )‐Diepoxy[18]annulene(10.0) – a Highly Dynamic Annulene The McMurry reaction of (all‐E)‐5,5′‐([2,2′‐bifuran]‐5,5′‐diyl)bis[penta‐2,4‐dienal] ( 13 ) only occurs intramolecularly to give a mixture of the diepoxy[18]annulenes(10.0) 6 and 7 . Tetraepoxy[36]annulene(10.0.10.0) resulting from an intermolecular McMurry reaction is not formed. According to spectroscopic data, 6 is (Z,E,Z,E,Z)‐ and 7 (Z,E,E,Z,E)‐configured. The 1H‐NMR data confirm that in 6 the (E)‐ethene‐1,2‐diyl bonds (C(11)=C(12) and C(15)=C(16)) rotate around the adjacent σ‐bonds. Beginning at −70°, this rotation freezes, and 6 is becoming a diatropic aromatic ring system. Beside [18]annulene itself, (Z,E,Z,E,Z)‐diepoxy[18]annulene(10.0) 6 is the only hitherto known [18]annulene derivative with dynamic properties. 相似文献
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Pter Molnr Jzsef Deli Erzsbet sz Zoltn Matus Gyula Tth Ferenc Zsila 《Helvetica chimica acta》2004,87(8):2169-2179
3′‐Epilutein (=(all‐E,3R,3′S,6′R)‐4′,5′‐didehydro‐5′,6′‐dihydro‐β,β‐carotene‐3,3′‐diol; 1 ), isolated from the flowers of Caltha palustris, was submitted to both thermal isomerization and I2‐catalyzed photoisomerization. The structures of the main products (9Z)‐ 1 , (9′Z)‐ 1 , (13Z)‐ 1 , (13′Z)‐ 1 , (15Z)‐ 1 , and (9Z,9′Z)‐ 1 were determined based on UV/VIS, CD, 1H‐NMR, and MS data. 相似文献
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6-O-(2-naphthoyl)curdlan was newly synthesized as a sensitizing polysaccharide host to examine the chiroptical properties, supramolecular complexation, and photochirogenic behavior with (Z,Z)-1,3-cyclooctadiene (1ZZ). The enantiodifferentiating photoisomerization of 1ZZ included and sensitized by this polysaccharide host gave a highly strained chiral (E,Z)-isomer in up to 8.7% enantiomeric excess (ee) in solution and 11.7% ee in the solid state, which are the highest values ever reported for a supramolecular photochirogenesis of 1EZ. 相似文献
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Easily accessible Ac-(Z)-delta Phe-NHMe was photoisomerized to so far unknown Ac-(E)-delta Phe-NHMe. Some parameters of the process leading to a diastereomeric mixture of ratio 90(Z):10(E) have been tested and the photoisomerization has been carried out on a preparative milligram scale. The isomers were separated via crystallization followed by preparative HPLC. 相似文献
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《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2017,129(46):14899-14903
The individual molecules of α‐chloroalkenyl boronates include both an electrophilic C−Cl bond and a nucleophilic C−B bond, which makes them intriguing organic synthons. Reported herein is a stereodivergent synthesis of both E and Z α‐chloroalkenyl N ‐methyliminodiacetyl (MIDA) boronates through the direct chlorination of alkenyl MIDA boronates using t BuOCl and PhSeCl reagents, respectively. Both reaction processes are stereospecific and the use of sp3‐B MIDA boronate is the key contributor to the reactivity. The synthetic value of the boronate products was also demonstrated. 相似文献