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101	Author	Markus Wollenweber2, Reinhart Keese3, Helen Stoeckli-Evansb	Requires cookie*
	Title	Synthesis of Spirocyclic Aminosilanes with Electron Withdrawing Substituents at Nitrogen
	Abstract	The first synthesis of spirocyclic tetrasulfonamidosilanes is described. According to the X-Ray structure analysis of the most stable tetratosylamidosilane obtained the Silicon is bonded to four Nitrogen atoms in a spirocycle and surrounded by four Oxygen atoms which are located above the planes of the SiN4 tetrahedron.
	Reference	Z. Naturforsch. 53b, 145—148 (1998); received October 24 1997
	Published	1998
	Keywords	Spirocyclic Sulfonamidosilanes, 1, 2-Phenylene Diamides, Capped Tetrahedron, X-Ray Data, Chelation
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	TEI-XML for	default:Reihe_B/53/ZNB-1998-53b-0145.pdf
	Identifier	ZNB-1998-53b-0145
	Volume	53

102	Author	Markus Leirer, Günther Knör, Amd Vogler	Requires cookie*
	Title	Synthesis and Spectroscopic Properties of 1,2-Diiminetricarbonyl- rhenium(I)chloride Complexes with Aliphatic Diimines (or 1,4-Diaza-l,3-butadienes) as Ligands
	Abstract	Re(l,2-diimine)(CO)3Cl complexes with the aliphatic bidentate ligands diiminosuccino-dinitrile (DISN), benzilbisanile (BEAN), bisacetylbisanile (BABA), and benzildiimine (BE DIM) are reported. The compounds show Re(I) to 7r(diimine) metal-to-ligand charge transfer (MLCT) absorptions in the visible spectral region. The energy of these MLCT-transitions de creases in the series BABA > BEDIM > BEAN > DISN, depending on the 7r acceptor properties of the coordinated diimine ligands. The maxima of these CT bands undergo a solvent-dependent shift (negative solvatochromism), which indicates a partial charge redistribution in the excited state. The compounds are not photoluminescent at room temperature and 77 K.
	Reference	Z. Naturforsch. 54b, 341—344 (1999); received December 11 1998
	Published	1999
	Keywords	Charge Transfer, Rhenium Complexes, 1, 4-Diaza-l, 3-butadienes, Solvatochromism
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	TEI-XML for	default:Reihe_B/54/ZNB-1999-54b-0341.pdf
	Identifier	ZNB-1999-54b-0341
	Volume	54

103	Author	Bernhard Schreiner, Reinhold Urban, Anastassios Zografidis, Karlheinz Sünkel, Kurt Polborn, Wolfgang Beck, *. Sonderdruckanforderungen, ProfW. Beck, Herrn Professor, LawrenceF. Dahl	Requires cookie*
	Title	Metallkomplexe mit biologisch wichtigen Liganden, CXXI [1]. Orthopalladierte Enolate aus N-(Diphenylmethylen)-Schiff-Basen von a-Aminosäureestern als ambivalente 1,3-Dipole in [2+3]-Cyclo- additionsreaktionen. Strukturen einer Reihe von Cycloaddukten Metal Complexes of Biologically Important Ligands, CXXI [1]. Orthopalladated Enolates from N-(Diphenylmethylene) Schiff Bases of a-Amino Acid Esters as Ambivalent 1,3-Dipoles in [2+3] Cycloadditions. Structures of a Series of Cycloadducts
	Abstract	Enolates of ortho-palladated N-(diphenylmethylene) Schiff bases from glycine esters (R3P)Pd[(C6H4)(C6H5)C=N-C(R')=C0 2R] were isolated and have been shown to be ambiva lent 1,3-dipoles in [2+3] cycloadditions. Tetracyanoethene, dimethyl acetylene dicarboxylate, dimethyl azodicarboxylate, thiobenzophenone, thione-S, 4-phenyl-l,2,4-triazoline-3,5-dione, diphenyl-ketene and phenylisocyanate are added at the palladium and the enolate (a-C) carbon atoms, whereas methyl propiolate, methyl acrylate, and the methyl esters of maleic and fumaric acid form [2+3] cycloadducts with the «-carbon and the imino carbon atoms of the enolates un der mild conditions. The structures of seven cycloadducts were determined by X-ray diffraction analyses.
	Reference	Z. Naturforsch. 54b, 970—988 (1999); eingegangen am 3. Mai 1999
	Published	1999
	Keywords	N-(Diphenylmethylene)glycinate, Enolates, 1, 3-Dipoles, [2+3] Cycloaddition, X-Ray Data
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	TEI-XML for	default:Reihe_B/54/ZNB-1999-54b-0970.pdf
	Identifier	ZNB-1999-54b-0970
	Volume	54

104	Author	MichaelC. Moschidis	Requires cookie*
	Title	Synthesis of l,2-Dipalmitoyloxypropyl-3-(2-ammoniumethyl) Phosphinate
	Abstract	The total synthesis of l,2-dipalmitoyloxypropyl-3-(2-ammoniumethyl) phosphinate, the phos-phino-analog of phosphatidyl ethanolamine is described. The phosphinate analog of phosphatidyl ethanolamine has been prepared by an Arbusov type of reaction between a diacyl-glycerol bromohydrin and 2-bromo-ethylphosphonic acid dimethyl ester for 48 h at 178 °C, followed by a reaction with aq. ammonia to yield the final product. The product was characterized by elemental analysis, phosphono-phosphorus determinations and IR spectroscopy.
	Reference	Z. Naturforsch. 40c, 595—598 (1985); received April 22 1985
	Published	1985
	Keywords	Phosphinolipids, Phosphatidyl Ethanolamine, 1, 2-Dipalmitoyl-sn-glycerol Bromohydrin, Phos-phino Analog of Phosphatidyl Ethanolamine
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	TEI-XML for	default:Reihe_C/40/ZNC-1985-40c-0595.pdf
	Identifier	ZNC-1985-40c-0595
	Volume	40

105	Author	Virginia Massheimer, LuisM. Fernandez, AnaR. De Boland	Requires cookie*
	Title	Stimulation of Calmodulin Binding to Skeletal Muscle Membrane Proteins by 1,25-Dihydroxy-Vitamin D 3
	Abstract	Previous work has shown that 1,25-dihydroxy-vitamin D 3 rapidly increases calmodulin lev els of skeletal muscle membranes without altering the muscle cell calmodulin content. There fore, the effects of the sterol on the binding of calmodulin to specific muscle membrane pro teins were investigated. Soleus muscles from vitamin D-deficient chicks were treated in vitro for short intervals (5-15 min) with physiological concentrations of 1,25-dihydroxy-vitamin D 3. Proteins of mitochondria and microsomes isolated by differential centrifugation were sep arated on sodium dodecyl sulfate polyacrylamide gels. Calmodulin-binding proteins were identified by a [125I]calmodulin gel overlay procedure followed by autoradiography. 1,25-Di-hydroxy-vitamin D 3 increased the binding of labelled calmodulin to a major, calcium-inde pendent, calmodulin-binding protein of 28 Kda localized in microsomes, and to minor calmo dulin-binding proteins of 78 and 130 Kda proteins localized in mitochondria. The binding of [125I]calmodulin to these proteins was abolished by flufenazine or excess non-radioactive cal modulin. 1,25-Dihydroxy-vitamin D 3 rapidly increased muscle tissue Ca uptake and cyclic AM P levels and stimulated the phosphorylation of several membrane proteins including those whose calmodulin-binding capacity potentiates. Analogously to the sterol, forskolin increased membrane calmodulin content, calmodulin binding to the 28 Kda microsomal protein and 45Ca uptake by soleus muscle preparations. Forskolin also induced a similar profile of changes in muscle membrane protein phosphorylation as the hormone. These results suggest that 1,25-dihydroxy-vitamin D 3 affects calmodulin distribution in muscle cells through cyclic AMP-de-pendent phosphorylation of membrane calmodulin-binding proteins. These changes may play a role in the stimulation of muscle Ca uptake by the sterol.
	Reference	Z. Naturforsch. 45c, 663—670 (1990); received October 2/November 3 1989
	Published	1990
	Keywords	1, 25-Dihydroxy-Vitamin D 3, Skeletal Muscle, Muscle Membranes, Calmodulin Binding, Protein Phosphorylation
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	TEI-XML for	default:Reihe_C/45/ZNC-1990-45c-0663.pdf
	Identifier	ZNC-1990-45c-0663
	Volume	45

106	Author	J. W. Wheeler3, L. Nyalley3, D. M. Davisb, P. J. Weldonc	Requires cookie*
	Title	Additional Sulfur Compounds from the Anal Glands of the Striped Polecat, Ictonyx striatus (Mustelidae, Mammalia)
	Abstract	Two sulfur compounds have been identified in the anal gland secretions of captive-raised adults of the striped polecat (Ictonyx striatus), an African mustelid. 3-Ethyl-l,2-pentanedithiolane was observed in the secre tions of an adult male and an adult female. 1,3-Pen tanedithiol was observed in the male; this compound has not previously been reported from mustelid anal glands.
	Reference	Z. Naturforsch. 52c, 283—285 (1997); received December 16 1996/February 4 1997
	Published	1997
	Keywords	Ictonyx striatus, Striped Polecat, Anal Gland Secretions, 3-Ethyl-l, 2-pentanedithiolane, 1, 3-Pentanedithiol
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	TEI-XML for	default:Reihe_C/52/ZNC-1997-52c-0283_n.pdf
	Identifier	ZNC-1997-52c-0283_n
	Volume	52

107	Author	Klaus Burger, Herbert Goth, Kurt Einhellig, Alfred Gieren	Requires cookie*
	Title	Zum Thermolyseverhalten von 2.2-Dihydro-1.4.2-oxazaphosphol-4-enen, I Über die Dimerisierung von bis(trifluormethyl)substituierten Nitril-yliden [1, 2] Thermolysis of 2,2-Dihydro-l,4,2-oxazaphosphol-4-enes, I Dimerization of Bis(trifluoromethyl) Substituted Nitrile Ylides [1, 2]
	Reference	Z. Naturforsch. 36b, 345—352 (1981); eingegangen am 18. November 1980
	Published	1981
	Keywords	I, 4, 2-Oxazaphosphoranes, 5->-[3 + 2]Cycloreversion Reactions, 1, 3-Dipole Dimerization, Head to Head Dimerization
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	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0345.pdf
	Identifier	ZNB-1981-36b-0345
	Volume	36

108	Author	WolfPeter Fehlhammer, Bartel Klaus, Dagobert Alfons Völkl, Achatz	Requires cookie*
	Title	Metallkomplexe funktioneller Isoeyanide, VI [1] Tosylmethyl-, Benzyl-und Benzhydrylisocyanid-Metallverbindungen und ihre Reaktionen mit Nucleophilen und 1.3-Dipolarophilen Metal Complexes of Functional Isocyanides, VI [1] Tosylmethyl-, Benzyl-and Benzhydrylisocyanide Metal Complexes and Their Reactions with Nucleophiles and 1,3-Dipolarophiles
	Abstract	Metal complexes of the type M(CO)5L (M = Cr, W), MX2L2 (M = Pd, Pt; X = Cl, Br, 1), PtClo(L)PPh3, and [Pt(Cl)(L)(PPh3)2]BF4 have been prepared with L = CNCH2S02C6H4-^CH3, CNCHoPh, and CNCHPho, and reacted with a variety of nucleophiles (NH2CH2C02CH3, CH(CN)2", CH(CN)C02CH3-, OH-) and 1,3-dipolarophiles (CF3CN, CH3O2CCEECCO2CH3, CH2 = CHCN, RNCO (R -CH3, Ph), RCHO (R = i-C3H7, Ph, C6H4-0OH)) to give carbene, a-aminovinyl, and carboxamido complexes, and C2-metallated heterocycles (imidazoles, pyrroles, oxazolos, oxazolines), respectively. Ready de-alkylation occurs of benzhydryl isoeyanide in [Pt(Cl)(CNCHPh2)(PPh3)2]BF4*
	Reference	Z. Naturforsch. 37b, 1044—1053 (1982); eingegangen am 5. Februar 1982
	Published	1982
	Keywords	Transition Metal Complexes of Functionalized Isocyanides, Reactions at Co-ordinated Ligands, Carbene Complexes, 1, 3-Dipolar Cycloadditions
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	TEI-XML for	default:Reihe_B/37/ZNB-1982-37b-1044.pdf
	Identifier	ZNB-1982-37b-1044
	Volume	37

109	Author	Yvonne Nagel, Wolfgang Beck	Requires cookie*
	Title	Metallkomplexe mit biologisch wichtigen Liganden, XLIII [1] Metallkomplexe mit ungeschützten acyclischen Monosaccharid-Derivaten (Amin-, Oxim-, Schiffbase-, Thiazolidin-und 1,3-Dithian-Liganden) Metal Complexes with Biologically Important Ligands, XLIII [1] Metal Complexes with Unprotected Acyclic Derivatives of Monosaccharides (Amine, Oxime, Schiffbase, Thiazolidine and 1,3-Dithiane Ligands)
	Abstract	The synthesis and spectroscopic data of palladium (II), platinum (II), nickel(II), cobalt(II), copper(II) and gold(I) complexes with D-glucose oxime, 2-amino-2-deoxy-D-glucose oxime, 1.2-diam ino-l,2-deoxy-D-glucitole, L-cysteine-D-glucose, D-glucose trim ethylene m ercaptale. Schiffbases from l,2-diam ino-l,2-deoxy-D -glucitole and acetylacetone or from D-glucosone and 1.3-diaminopropane are reported.
	Reference	Z. Naturforsch. 41b, 1447—1454 (1986); eingegangen am 7. Juli 1986
	Published	1986
	Keywords	Derivatives of Polyalcohols, Schiffbase, Thiazolidine, 1, 3-Dithiane Complexes of Platinum, Palladium, Nickel and Cobalt
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	TEI-XML for	default:Reihe_B/41/ZNB-1986-41b-1447.pdf
	Identifier	ZNB-1986-41b-1447
	Volume	41

110	Author	D. Ieter Fenske, Christina Ergezinger, Kurt Dehnicke	Requires cookie*
	Title	Crystal Structure of l,l-D ichloro-3,5- diphenyl-4-H-l,2.4,6-/.4-selenatriazine, SeCl2C2N 3H (C 6H 5)2
	Reference	Z. Naturforsch. 44b, 857—8 (1989); eingegangen am 15. Februar 1989
	Published	1989
	Keywords	1, l-D ichloro-3, 5-diph en yl-4-H -l, 2, 46-Ä4-selenatriazine, Preparation, Crystal Structure
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	TEI-XML for	default:Reihe_B/44/ZNB-1989-44b-0857_n.pdf
	Identifier	ZNB-1989-44b-0857_n
	Volume	44

111	Author	N. Orbert Auner, Erika Penzenstadler	Requires cookie*
	Title	Silaheterocyclen, XVII Synthese und Cycloadditionsreaktionen neuartiger, aminocyclischer Silaethene [1] Silaheterocycles, XVII Synthesis and Cycloaddition Reactions of Novel Amino Cyclic Silenes [1]
	Abstract	The silene 2 is formed by reacting 2-chloro-l,3-bis(trimethylsilyl)-2-vinyl-1,3-diaza-2-silacyclopentane (5) with LiBu' in «-pentane in the tem perature range from -1 0 to +10 °C. The reaction primarily leads to the corresponding a-lithio adduct 6 by addition of the Li-organyl to the vinyl group o f 5; subsequent 1,2-LiCl elimination yields 2 as an intermediate. 2 can be trapped by polar reagents M e3SiX (X = OMe, 0 S 0 2C F 3) as well as by organic dienes which add across the Si = C bond; in the absence of trapping agents, trisilacyclohexane 7 is isolated. The cycloaddition behaviour of 2 is best described by the two mesomeric formulae (a) and (ß), with competitive [4+2] and [2 + 2] addition routes: While with butadienes and norbor-na-2,5-diene the [2 + 2] products are formed mainly in a multiple step reaction via zwitterionic intermediates (1,4 dipoles), the ratio o f the [4+2]/[2 + 2] derivatives from 2 and cyclohexa-1,3-diene becomes nearly equivalent. 2 is thus quite com parable in its reactivity to dichloro-neopentylsilene, Cl2Si = C H C H 2Bu'.
	Reference	Z. Naturforsch. 47b, 795—804 (1992); eingegangen am 25. November 1991
	Published	1992
	Keywords	Silaheterocycles, Synthesis, 1, 3-Bis(trimethylsilyl)-1, 3-diaza-2-silacyclopentane, F orm ation o f Silenes, Cycloaddition Reactions
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	TEI-XML for	default:Reihe_B/47/ZNB-1992-47b-0795.pdf
	Identifier	ZNB-1992-47b-0795
	Volume	47

112	Author	Neda, Michael Farkens, Holger Thönnessen, PeterG. Jones, Reinhard Schmutzler	Requires cookie*
	Title	Zur Chemie der l,3,5-Triaza-2-phosphorinan-4,6-dione. Teil X*. Umsetzungen von 2-Hydro
	Abstract	l,3,5-trimethyl-l,3,5-triaza-2-oxo-2A4-phosphorinan-4,6-dion mit Triazin-Derivaten sowie mit einigen Aldehyden Chemistry of the l,3,5-Triaza-2-phosphorinan-4,6-diones. Part X*. Reactions of 2-H ydro-1,3,5-trim ethyl-1,3,5-triaza-2-oxo-2A4-phosphorinan-4,6-dione with Triazine Derivatives and with Some Aldehydes Ion
	Reference	Z. Naturforsch. 50b, 1833—1 (1995); eingegangen am 8. Mai 1995
	Published	1995
	Keywords	1, 3, 5-Trimethyl-Substituted l, 3, 5-Triaza-2A 4 -phosphorinan-4, 6-diones, NM R Spectra, Mass Spectra, X-Ray
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	TEI-XML for	default:Reihe_B/50/ZNB-1995-50b-1833.pdf
	Identifier	ZNB-1995-50b-1833
	Volume	50

113	Author	Z. Naturforsch	Requires cookie*
	Title	Elektronentransfer und Ionenpaar-Bildung
	Abstract	, 47 [1] Titrationen von 1,2,4,5-Tetracyanbenzol und 7,7,8,8-Tetracyan-/;-chino-dimethan mit Natriummetall in aprotischen Lösungen E le ctro n T ran sfer an d Ion P air F o rm atio n , 47 [ 1 ] T itratio n s o f 1,2 ,4 ,5 -T etracy an o b en zen e and 7 ,7 ,8 ,8 -T etracy an o -/?-q u in o d im eth an e w ith S o d iu m M etal in A p ro tic S o lu tio n s H an s B ock*, M a rk u s K leine
	Reference	Z. Naturforsch. 51b, 1215—1221 (1996); eingegangen am 25. Januar 1996
	Published	1996
	Keywords	1, 2, 4, 5-Tetracyanobenzene, 7, 7, 8, 8-Tetracyano-/?-quinodimethane, Sodium Metal Reduction, UV/VIS Spectra
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	TEI-XML for	default:Reihe_B/51/ZNB-1996-51b-1215.pdf
	Identifier	ZNB-1996-51b-1215
	Volume	51

114	Author	Vasily	Requires cookie*
	Title	Chemistry of the l,3>5-Triaza-2-phosphorin-4,6-diones, Part XII*. Synthesis and Characterization of 2-PhenyI-2-(/?-tolylthio)-l,3?5- trimethyI-l,3,5-triaza-4,6-dione-2-phosphorinonium Salts
	Abstract	A . P in ch u k , Io n N e d a , C h ristian M üller, H o lg e r T h ö n n e ss e n , P e te r G. Jones, R e in h a rd S chm utzler The reaction of l,5-bis(trimethylsilyl)-l,3.5-trimethylbiuret (1) with/M olylsulfenyl chloride (2) furnished l-(/?-tolylthio)-5-trimethylsilyl-l,3,5-trimethylbiuret (3). In the reaction of 3 with phenyldichlorophosphine, 2-phenyl-2-(/?-tolylthio)-l,3,5-trimethyl-l,3,5-triaza-4,6-dione-2-phosphorinonium chloride (4) was formed. The same product was obtained from the reac tion of 2-phenyl-l,3,5-trimethyl-l,3,5-triaza-2/.3-phosphorin-4,6-dione (6) with p-tolylsulfenyl chloride (2). Compound 4 was isolated and characterized in the form of the hexachloroanti-m onate (4a). The spirophosphorane 2-phenyl-l,3,5-trimethyl-l,3,5-triaza-7,10-dioxa-8,9-perchlorobenzo-2As-phosphaspiro-[4.5]decan-4,6-dione (7) was prepared by the reaction of 4 with tetrachloroorthobenzoquinone. The new products were characterized by 'H -and 13C NMR spectroscopy, elemental analysis, 31P NMR spectroscopy in the case of 4a. 6 and 7, and mass spectrometry (4a). Single-crystal X-ray structural analyses of compounds 4a and 7 were conducted. The phosphorus atom of 4a has the expected tetrahedral geometry, with a rather short P-S bond of 204.9(2) pm. In 7 the geometry at phosphorus is almost ideal trigonal bipyramidal. Weak hydrogen bonds are formed from a C (:0) group to deuterochloroform of solvation.
	Reference	Z. Naturforsch. 51b, 1494—1500 (1996); received February 13 1996
	Published	1996
	Keywords	1, 3, 5-Trimethyl-Substituted 1, 3, 5-Triaza-4, 6-dione-2-phosphorinonium Derivatives, Intram olecular Rearrangem ent, NMR Spectra, X-Ray
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	TEI-XML for	default:Reihe_B/51/ZNB-1996-51b-1494.pdf
	Identifier	ZNB-1996-51b-1494
	Volume	51

115	Author	G. Unther Seitz, Johanna Siegl	Requires cookie*
	Title	Synthese neuer Pyridin-C-nukleoside der 2 ,3 -D i d e s o x y r i b o s e durch "inverse" [4+2]-Cycloaddition Synthesis of Novel Pyridine-C-nucleosides of 2,3-Dideoxyribose by "Inverse" [4+2]-Cycloaddition
	Abstract	The anomeric imido esters 5 and 6, appropriate precursors for C-nucleoside synthesis, were prepared and utilized as heterodienophiles in a Diels-Alder reaction with inverse electron
	Reference	Z. Naturforsch. 52b, 851—858 (1997); eingegangen am 22. April 1997
	Published	1997
	Keywords	Pyridine-C-nucleosides, "Inverse" [4+2] Cycloadditions, 1, 2, 4-Triazine-C-nucleosides, 2, 3'-Dideoxy-/?-D-ribofuranosyl-pyridines
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	TEI-XML for	default:Reihe_B/52/ZNB-1997-52b-0851.pdf
	Identifier	ZNB-1997-52b-0851
	Volume	52

116	Author	Erhard Jägers, Bert Steffan, R. Enata Von Ardenne, Wolfgang Steglich	Requires cookie*
	Title	Stoffw echselprodukte des
	Abstract	2.4-Trihydroxy-benzols aus Fruchtkörpern von G om phidius m aculatus und G. glutinosus (B oletales) [1] M etabolites of 1,2,4-Trihydroxybenzene from Fruiting Bodies o f Gomphidius maculatus and G. glutinosus (Boletales) [1]
	Reference	Z. Naturforsch. 36c, 488—4 (1981); received February 25 1981
	Published	1981
	Keywords	Gomphidius, Boletales, 1, 2, 4-Trihydroxybenzene, 2, 2', 4, 4', 5, 5'-Hexahydroxybiphenyl, Gomphilactone, Postemak Rearrangement
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	TEI-XML for	default:Reihe_C/36/ZNC-1981-36c-0488_n.pdf
	Identifier	ZNC-1981-36c-0488_n
	Volume	36

117	Author	Klaus Burger, Herbert Goth	Requires cookie*
	Title	Positionsselektivität und Regiochemie bei Abfangreaktionen mit Heterokumulenen Cycloaddition Behaviour of Bis(trifluoromethyl) Substituted Nitrile Ylides [1] Site Selectivity and Regiochemistry of Trapping Reactions with Heterocumulenes
	Abstract	3,3-bis(trifluoromethyl)-2,2-dihydro-l,4,2-oxazaphosphol-4-enes on thermolysis undergo a 1,3-dipolar cycloreversion reaction with formation of bis(trifluoro-methyl) substituted nitrile ylides and trimethyl phosphate. The nitrile ylides are trapped by N-8ulfinyl aniline, phenyl isocyanate, phenyl isothiocyanate, diphenyl ketene, and carbon disulfide. Site selectivity and regiochemistry of the [3 + 2]cycloaddition reactions are described. The results are compared with those obtained from [3 + 2]cycloaddition reactions of nitrile imines, nitrile oxides, alkyl, and aryl substituted nitrile ylides with heterocumulenes.
	Reference	Z. Naturforsch. 37b, 473—485 (1982); eingegangen am 30. September 1981
	Published	1982
	Keywords	1, 3-Dipolar Cycloreversion Reactions, 2, 2-Dihydro-l, 4, 2-oxazaphosphol-4-enes, Trifluoromethyl Substituted 1, 3-Dipoles, Partially Fluorinated Heterocyclic Compounds 2, 2, 2-Trimethoxy-
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	TEI-XML for	default:Reihe_B/37/ZNB-1982-37b-0473.pdf
	Identifier	ZNB-1982-37b-0473
	Volume	37

118	Author	Michael Farkens, ThomasG. Meyer, Ion Neda, R.Alf Sonnenburg, Christian Müller, AxelK. Fischer, PeterG. Jones, Reinhard Schmutzler	Requires cookie*
	Title	Zur Chemie der l,3,5-Triaza-2-phosphinan-4,6-dione. Teil VI*. Darstellung von l,3>5-Triaza-2 A3
	Abstract	, l,3,5-Triaza-2 A4-und 1,3,5-T riaza-2 A5-phosphinan-4,6-dionen Chemistry o f the l,3,5-Triaza-2-phosphinane-4,6-diones. Part VI. Synthesis o f l,3,5-Triaza-2^3-, 1,3,5-Triaza-2A4-and l,3,5-Triaza-225-phosphinane-4,6-diones The reactions o f 1,3,5-trimethylbiuret with dicyclohexylam inodichlorophosphine and with pyrrolidinodichlorophosphine furnished the triazaphosphinane-diones 1 and 2. Oxidation
	Reference	Z. Naturforsch. 49b, 145—164 (1994); eingegangen am 29. Juli 1993
	Published	1994
	Keywords	1, 3, 5-Triorgano-Substituted l, 3, 5-Triaza-2-phosphinan-4, 6-diones, Oxidation Reactions, N M R Spectra, M ass Spectra, X -R ay
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	TEI-XML for	default:Reihe_B/49/ZNB-1994-49b-0145.pdf
	Identifier	ZNB-1994-49b-0145
	Volume	49

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