ChemInform Abstract: Synthesis of a New Class of Asymmetric Ketone Reduction Catalyst via a Diastereoselective Cyclization Reaction: X-Ray Crystal Structure of S( P)R-(-)-N-(tert-Butyldiphenylsilyl)dihydrobenzazaphosphole Oxide.

ChemInform ◽  
2010 ◽  
Vol 25 (3) ◽  
pp. no-no
Author(s):  
B. BURNS ◽  
E. MERIFIELD ◽  
M. F. MAHON ◽  
K. C. MOLLOY ◽  
M. WILLS
2017 ◽  
Vol 68 (6) ◽  
pp. 1159-1162
Author(s):  
Ionel Humelnicu ◽  
Violeta Vasilache

The synthesis and X-ray crystal structure of a new class of fused heterocycle with 8,9-dihydro-pyridazino[1,2,4]triazine type 2 is reported. The synthesis is facile and efficient and, the structure of compounds was proven by elemental and spectral analysis, the X-ray spectra including (for 2b). The compound crystallizes in the space group P21/N (monoclinic) with a = 9.0077(2) �, b = 10.20019(18) �, c = 14.0099(3) �, a= 90�, b = 89.768(2)�, g= 90�, V= 1287.22(5) and Z = 4. Accurate molecular parameters for the heterocyclic system were obtained from intensity data collected at 200(14) K. The molecule 8,9-dihydro-pyridazino[1,2,4]triazine type 2 is a noncoplanar bicyclic fused system, with an envelope shape onto the triazine moiety, the C12 carbon being out of plane. The methyl group from the C12 carbon it is almost perpendicular on the triazine plane. We also notice a rather powerful hydrogen bond between hydrogen atom from N1 and the oxygen from the C11=O1 carbonyl group.


Synthesis ◽  
2020 ◽  
Vol 52 (23) ◽  
pp. 3622-3631
Author(s):  
Victor V. Fedotov ◽  
Evgeny N. Ulomsky ◽  
Konstantin V. Savateev ◽  
Evgeny M. Mukhin ◽  
Denis A. Gazizov ◽  
...  

A highly efficient PASE approach to a new class of polycyclic purine derivatives has been proposed. The strategy includes a consecutive reduction, auto-aromatization, and heterocyclization of the initial nitrobenzimidazopyrimidines obtained by a three-component condensation. It was shown that reduction of nitrobenzimidazopyrimidines by metals in acidic media was more efficient than heterogeneous hydro­genation. Novel derivatives of benz[4,5]imidazo[1,2-a]purines were obtained­ in good yields and the proposed structure was confirmed by X-ray crystal structure analysis. The obtained convergent benzimidazopurines combine two relevant medicinal chemistry scaffolds – benz­imidazole and purine.


1980 ◽  
Vol 21 (20) ◽  
pp. 1961-1962 ◽  
Author(s):  
Izhar H. Qureshi ◽  
Shaheen A. Husain ◽  
Radia Noorani ◽  
Najma Murtaza ◽  
Yoichi Iitaka ◽  
...  
Keyword(s):  
X Ray ◽  

1999 ◽  
Vol 55 (2) ◽  
pp. 165-169 ◽  
Author(s):  
Peter Alberius Henning ◽  
Sven Lidin ◽  
Vačlav Petříček

Iodo-oxyapatite [pentadecacalcium iodide oxide nonaphosphate, Ca15(PO4)9IO] was synthesized by a flux method and the structure was solved from single-crystal X-ray data. The crystal structure was refined in the space group P63/m [a = 9.567 (1), c = 20.754 (2) Å and Z = 2] to wR on F of 0.0459. Iodo-oxyapatite has a typical hexagonal apatite structure but the unit cell is tripled along the hexad owing to ordering of the iodide and oxide ions along this direction.


1989 ◽  
Vol 44 (6) ◽  
pp. 659-665 ◽  
Author(s):  
Ulf Pindur ◽  
Ludwig Pfeuffer ◽  
Camran Flo ◽  
Werner Massa ◽  
Karin Seitz

The conformations of and charge distributions in indolyl(alkoxy)carbenium tetrafluoroborates 2, a new class of highly stabilized carbenium ions, were investigated by 1H and 13C NMR spectroscopy and the crystal structure of indol-3-yl(methoxy)phenylcarbenium tetrafluoroborate (2e) was determined by X-ray diffraction methods. The phenyl-substituted cation of 2e exhibits axial chirality in the crystalline state


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