ChemInform Abstract: REGIOSELECTIVE ACID-CATALYZED CYCLODIMERIZATION OF 1,2-DIHYDRONAPHTHALENE. MECHANISM OF FORMATION AND SINGLE-CRYSTAL X-RAY ANALYSIS OF TWO OCTAHYDROBENZO(J)FLUORANTHENES

1981 ◽  
Vol 12 (16) ◽  
Author(s):  
T. K. DOBBS ◽  
D. V. HERTZLER ◽  
G. W. KEEN ◽  
E. J. EISENBRAUN ◽  
R. FINK ◽  
...  
Keyword(s):  
Single Crystal ◽  
Mechanism Of Formation ◽  
X Ray ◽  
Acid Catalyzed

Regioselective acid-catalyzed cyclodimerization of 1,2-dihydronaphthalene. Mechanism of formation and single-crystal x-ray analysis of two octahydrobenzo[j]fluoranthenes

1980 ◽  
Vol 45 (23) ◽  
pp. 4769-4774 ◽  
Author(s):  
Thomas K. Dobbs ◽  
Donald V. Hertzler ◽  
Gary W. Keen ◽  
Edmund J. Eisenbraun ◽  
Robert Fink ◽  
...  
Keyword(s):  
Single Crystal ◽  
Mechanism Of Formation ◽  
X Ray ◽  
Acid Catalyzed

Acid-catalyzed cyclization of 3,3',4,4'-tetrahydro-1,1'-binaphthyl and single-crystal x-ray structure determination of a polycyclic stable ozonide

1984 ◽  
Vol 49 (6) ◽  
pp. 1030-1033 ◽  
Author(s):  
Thomas K. Dobbs ◽  
Arnold R. Taylor ◽  
Julie A. Barnes ◽  
Belma D. Iscimenler ◽  
Elizabeth M. Holt ◽  
...  
Keyword(s):  
Single Crystal ◽  
Structure Determination ◽  
X Ray ◽  
Acid Catalyzed

scholarly journals A one-pot multistep cyclization yielding thiadiazoloimidazole derivatives

2014 ◽  
Vol 10 ◽  
pp. 2989-2996 ◽  
Author(s):  
Debabrata Samanta ◽  
Anup Rana ◽  
Jan W Bats ◽  
Michael Schmittel
Keyword(s):  
Single Crystal ◽  
Mechanism Of Formation ◽  
One Pot ◽  
X Ray ◽  
Dft Computations ◽  
Methanesulfonyl Chloride ◽  
Intramolecular Reaction ◽  
Synthetic Procedure

A versatile synthetic procedure is described to prepare the benzimidazole-fused 1,2,4-thiadiazoles 2a–c via a methanesulfonyl chloride initiated multistep cyclization involving the intramolecular reaction of an in-situ generated carbodiimide with a thiourea unit. The structure of the intricate heterocycle 2a was confirmed by single-crystal X-ray analysis and its mechanism of formation supported by DFT computations.

scholarly journals Acid catalyzed cyclodimerization of 2,2-bis(trifluoromethyl)-4-alkoxy-oxetanes and -thietanes. Synthesis of 2,2,6,6-tetrakis(trifluoromethyl)-4,8-dialkoxy-1,5-dioxocanes and 3,3,7,7-tetrakis(trifluoromethyl)-9-oxa-2,6-dithia-bicyclo[3.3.1]nonane

2010 ◽  
Vol 6 ◽  
Author(s):  
Viacheslav A Petrov ◽  
Will Marshall
Keyword(s):  
Single Crystal ◽  
High Yield ◽  
X Ray Diffraction ◽  
X Ray ◽  
Acid Catalyzed ◽  
Yield Formation ◽  
Spontaneous Reaction

Treatment of 2,2-bis(trifluoromethyl)-4-R-oxetanes (R = C2H5O, n-C3H7O, n-C4H9O) with BF3·OEt2 in CH2Cl2 solvent results in spontaneous electrophilic [4 + 4] cyclodimerization with the formation of the corresponding 2,2,6,6-tetrakis(trifluoromethyl)-4,8-dialkoxy-1,5-dioxocanes, isolated in 31–42% yield. The structures of two products (R = C2H5O and n-C3H7O) were established by single crystal X-ray diffraction. The corresponding oxetane carrying the bulky t-C4H9O group has different reactivity towards BF3·OEt2, slowly producing a mixture of two acyclic, unsaturated products. Clean and spontaneous reaction with alcohols is another interesting transformation of oxetanes described in this paper. The reaction leads to high yield formation of the corresponding acetals (CF3)2C(OH)CH2CH(OR)OR′. Structurally related 2,2-bis(trifluoromethyl)-4-R-thietanes (R = i-C3H7O, t-C4H9O and C2H5O) have different reactivity towards electrophiles. They are totally inert to the action of BF3·OEt2 and rapidly react with a protic acid (H2SO4) forming the same product, 3,3,7,7-tetrakis(trifluoromethyl)-9-oxa-2,6-dithia-bicyclo[3.3.1]nonane in 35–50% yield. The structure of this product was established by single crystal X-ray diffraction.

scholarly journals A Chiral Sulfoxide-Based C–H Acid

Synlett ◽  
2021 ◽  
Author(s):  
Benjamin List ◽  
Denis Höfler ◽  
Karl Kaupmees ◽  
Ivo Leito
Keyword(s):  
Single Crystal ◽  
Lewis Acid ◽  
Absolute Configuration ◽  
X Ray ◽  
Design And Synthesis ◽  
High Acidity ◽  
Acid Catalyzed ◽  
Brønsted And Lewis Acid

We report the design and synthesis of a strong, chiral, enantiopure sulfoxide-based C–H acid. Single crystal X-ray analysis confirms the proposed structure and its absolute configuration. The new motif shows a high acidity and activity in Brønsted and Lewis acid catalyzed transformations. So far, only low enantioselectivities were achieved.

scholarly journals Synthesis and Structure Elucidation of N′-(4-Methoxybenzylidene)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carbohydrazide

Molbank ◽  
10.3390/m1034 ◽  
2018 ◽  
Vol 2018 (4) ◽  
pp. M1034 ◽  
Author(s):  
Mohammad Alotaibi ◽  
Hanan Mohamed ◽  
Bakr Abdel-Wahab ◽  
Amany Hegazy ◽  
Benson Kariuki ◽  
...  
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Single Crystal ◽  
Mass Spectroscopy ◽  
Structure Elucidation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Acid Catalyzed ◽  
Nuclear Magnetic

N′-(4-Methoxybenzylidene)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carbohydrazide (3) was synthesized in a yield of 88% from an acid-catalyzed reaction of 5-methyl-1-phenyl-1H-1,2,3- triazole-4-carbohydrazide and 4-methoxybenzaldehyde in ethanol under reflux for 2.5 h. The structure of 3 was confirmed by the data obtained from infrared, nuclear magnetic resonance, mass spectroscopy, single crystal X-ray diffraction, and microanalysis.

Electron Microscopy of Shock Loaded Polycrystalline Beryllium

1974 ◽  
Vol 32 ◽  
pp. 506-507 ◽  
Author(s):  
J. M. Galbraith ◽  
L. E. Murr ◽  
A. L. Stevens
Keyword(s):  
Electron Microscopy ◽  
Wave Propagation ◽  
Structural Change ◽  
Single Crystal ◽  
Diffraction Pattern ◽  
Shock Loading ◽  
Slip Systems ◽  
Compression Tests ◽  
X Ray Diffraction ◽  
X Ray

Uniaxial compression tests and hydrostatic tests at pressures up to 27 kbars have been performed to determine operating slip systems in single crystal and polycrystal1ine beryllium. A recent study has been made of wave propagation in single crystal beryllium by shock loading to selectively activate various slip systems, and this has been followed by a study of wave propagation and spallation in textured, polycrystal1ine beryllium. An alteration in the X-ray diffraction pattern has been noted after shock loading, but this alteration has not yet been correlated with any structural change occurring during shock loading of polycrystal1ine beryllium.This study is being conducted in an effort to characterize the effects of shock loading on textured, polycrystal1ine beryllium. Samples were fabricated from a billet of Kawecki-Berylco hot pressed HP-10 beryllium.

Crystal structure of an inclusion complex between chiral monoaza-15-crown-5 and S(–)-1-phenyl-ethyl ammonium percholorate

2003 ◽  
Vol 218 (5) ◽  
Author(s):  
Süheyla Özbey ◽  
F. B. Kaynak ◽  
M. Toğrul ◽  
N. Demirel ◽  
H. Hoşgören
Keyword(s):  
Crystal Structure ◽  
Inclusion Complex ◽  
Single Crystal ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
New Type

AbstractA new type of inclusion complex, S(–)-1 phenyl ethyl ammonium percholorate complex of R-(–)-2-ethyl - N - benzyl - 4, 7, 10, 13 - tetraoxa -1- azacyclopentadecane, has been prepared and studied by NMR, IR and single crystal X-ray diffraction techniques. The compound crystallizes in space group

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