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Volumn , Issue 20, 2006, Pages 3464-3468

Chemistry of polyhalogenated nitrobutadienes, 3: [4+2] cycloadditions of (Z)-1,1,4-trichloro-2,4-dinitrobuta-1,3-diene and subsequent reactions

(4) Zapol'skii, Viktor A a Namyslo, Jan C a Blaschkowski, Björn a Kaufmann, Dieter E a

a CLAUSTHAL UNIVERSITY OF TECHNOLOGY (Germany)

Author keywords

Cycloaddition; Diels Alder; Haloalkene; Heterocycle; Nitro compound

Indexed keywords

1,1,4 TRICHLORO 2,4 DINITROBUTA 1,3 DIENE; 1,2 DICHLOROETHYLENE; BENZIMIDAZOLE DERIVATIVE; BENZOXAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CYCLOADDITION; DIMERIZATION; NITRATION; SYNTHESIS;

EID: 33845966730 PISSN: 09365214 EISSN: None Source Type: Journal
DOI: 10.1055/s-2006-956490 Document Type: Article

Times cited : (22)

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- Crystal Data for 9. C15H12ClN 3O5, M, 349.73 g mol 1, crystal size 0.2 × 0.2 × 0.5 mm were collected on a Stoe IPDS II diffractometer using λ, 0.71073 Å [T, 223(2) K, The crystal structure was solved by direct methods and refined by full matrix least squares on F2 (SHELX-97) in the space group P21/n (monoclinic, lattice parameters a, 7.2336(12) Å, b, 19.414(3) Å, α, 10.834(2) Å, β, 96.523(15)°, V, 1511.7(4) Å3, Z, 4, dcalc, 1.537 g cm-3, F(000, 720, absorption coefficient, 0.286 mm-1 using 2682 independent reflections and 265 parameters. R1, 0.0489, wR2, 0.0995 [I > 2σI, goodness of fit on F2, 0.971, residual electron density, 0.203 and -0.267 e Å 3. CCDC 278475 contains supplementary crystallographic data f
- 3. CCDC 278475 contains supplementary crystallographic data for this paper, obtainable free of charge from www.ccdc.cam.ac.uk or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44(1223)336033; or deposit@ccdc.cam.ac.uk.

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- Experimental Details. Melting points were measured on a Büchi 520 apparatus and were uncorrected. 1H NMR, 13C NMR, 14N NMR, and 15N NMR spectra were obtained on a Bruker Avance with 400 MHz proton frequency, 15N NMR were measured in inverse 2D mode (gs-HMBC, 1H NMR spectra in CDCl3 were referenced to tetramethylsilane (TMS) at δ, 0.0 ppm; 13C NMR spectra refer to the solvent signal center at δ, 77.0 ppm. Other solvents as follows: DMSO-d6: 2.50 ppm (1H, 39.70 ppm (13C, CD3)2CO: 2.04 ppm (1H, 29.8 ppm (13C, C6D6: 7.20 ppm (1H, 128.0 ppm 13C, N NMR spectra were externally referenced to nitromethane at δ, 0.0 ppm. IR spectra were obtained on a Bruker 'Vector 22' FT IR as KBr IR. Mass spectra were recorded on a Hewlett Packard system 'M
- 2)

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