ALBERT — All Library Books, journals and Electronic Records Telegrafenberg

1

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Neue Wege zu 1H- und 2H-Pyrrolen (1980)

Pfoertner, Karl-Heinz ; Foricher, Joseph

New York, NY : Wiley-Blackwell

Helvetica Chimica Acta 63 (1980), S. 658-663

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ISSN: 0018-019X

Keywords: Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: New Routes to 1H- and 2H-PyrrolesA synthesis of 1H-pyrroles is described starting with pyridine analogues of chalcones and involving the reaction of acetic anhydride with 1-pyrroline-1-oxides. Another route leads from 1-pyrrolines to 2 H-pyrroles via bromination with N-bromosuccinimide and subsequent dehydrobromination in dimethylformamide.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/hlca.19800630313

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2

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Erratum (1980)

New York, NY : Wiley-Blackwell

Helvetica Chimica Acta 63 (1980), S. 681-681

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ISSN: 0018-019X

Keywords: Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/hlca.19800630317

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3

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Nucleophilic addition to C,C double bonds. IIIFor Part I, see [1]; for Part II, see [2].. Chemical reactivity of 1endo, 4endo: 5exo, 8exo-dimethano-1,2,3,4,4a,5,8,8a-octahydronaphthalen-10syn-ol and X-ray structure analysis of its p-nitrobenzoate (1980)

Pfund, Rolland A. ; Bernd Schweizer, W. ; Ganter, Camille

New York, NY : Wiley-Blackwell

Helvetica Chimica Acta 63 (1980), S. 674-681

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ISSN: 0018-019X

Keywords: Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: The title compound 1 is a further example of an olefinic alcohol that undergoes ether formation under basic conditions (→ 3) although the double bond is not activated by an electron-attracting group. This unusual reactivity is due to steric compression, which is increased in the 10-methyl analogue 2. This forms the corresponding ether 7 at a much higher rate. - In a deuteriated medium, base-catalysed cyclization of 1 gives the exo-deuteriated ether 6, corresponding to trans-addition. - An X-ray structure analysis of 4, the p-nitrobenzoate of 1, is presented.

Additional Material: 3 Ill.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/hlca.19800630316

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4

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The Synthesis of β,γ- and α,β-Unsaturated Aldehydes via Polyene EpoxidesDedicated to Dr. O. Isler on the occasion of his 70th birthday (1980)

Rosenberger, Michael ; Jackson, William ; Saucy, Gabriel

New York, NY : Wiley-Blackwell

Helvetica Chimica Acta 63 (1980), S. 1665-1674

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ISSN: 0018-019X

Keywords: Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: A substitute for the Darzens glycidic ester synthesis for converting unsaturated ketones or aldehydes into the homologated β,γ- or α,β-unsaturated aldehydes employing sulfur ylides is described. The carbonyl group is converted into the unsaturated oxirane which is then rearranged to the new aldehyde. High yields of isomerically pure aldehydes are available by this method and the process is of practical importance in the conversion of β-ionone into the β-C14-aldehyde, a key intermediate in the Isler synthesis of vitamin A. The efficient preparation of α- and β-cyclocitral by the novel process is also described.

Additional Material: 2 Tab.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/hlca.19800630636

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5

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Globularifolin, A New Acyl Iridoid Glucoside from Globularia cordifoliaPart 3 in the series ‘Glycosides of Globulariaceae’. For parts 1 and 2 see [1] [2]. (1980)

Chaudhuri, Ratan K. ; Sticher, Otto

New York, NY : Wiley-Blackwell

Helvetica Chimica Acta 63 (1980), S. 117-120

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ISSN: 0018-019X

Keywords: Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: Six iridoid glucosides have been isolated from Globularia cordifolia by the combination of open column - and high performance liquid chromatography. The structure of the new compound, named globularifolin, and the identity of the others have been established by chemical transformations and spectral evidence of the compounds and their derivatives.

Additional Material: 1 Tab.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/hlca.19800630112

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6

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Photofragmentation of Dibenzyl Ketone in the Presence of Tetramethylpiperidine Derivatives. Studies on light stabilizer mechanisms [1] (1980)

Felder, Bruno ; Schumacher, Rolf ; Sitek, Franciszek

New York, NY : Wiley-Blackwell

Helvetica Chimica Acta 63 (1980), S. 132-147

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ISSN: 0018-019X

Keywords: Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: The interaction of selected tetramethylpiperidine derivatives with radicals arising from the Norrish-type I cleavage of dibenzyl ketone under oxygen was studied. Product analyses and kinetic studies showed that the investigated sterically hindered piperidine derivatives have a pronounced effect on both the nature and distribution of the products of photolysis of dibenzyl ketone in the presence of oxygen. Observations indicated that the phenylperacetoxyl radical is formed as an intermediate during irradiation and that it interacts with the additives used. Possible mechanisms of the reactions studied are discussed.The observation that oxidation of an isolated double bond by the radicals formed in dibenzyl ketone photolysis under oxygen is strongly inhibited in the presence of the studied sterically hindered amines is discussed in the light of the results presented. The findings are considered in relation to the problem of polymer stabilization.

Additional Material: 6 Ill.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/hlca.19800630114

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7

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Approaches to the Synthesis of Cytochalasans. Part 2. Pyrrolinone derivatives as basic unitsPart 1: [1].Part of the Ph.D. Thesis of T. Schmidlin, Basel 1979. (1980)

Schmidlin, Tibur ; Tamm, Christoph

New York, NY : Wiley-Blackwell

Helvetica Chimica Acta 63 (1980), S. 121-131

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ISSN: 0018-019X

Keywords: Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: Several attempts to prepare 3-acetyl-5-benzyl-3-pyrrolin-2-one (7) from phenylalanine are described. This goal was only reached formally, because compound 7 exists in the tautomeric form of (Z)-5-benzyl-3-(1′-hydroxyethylidene)-4-pyrrolin-2-one (17) according to the spectral data. The problem of tautomerism in pyrrolinone systems is discussed.

Additional Material: 4 Ill.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/hlca.19800630113

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8

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Nucleophile Aminoalkylierung mit ThiopivalamidenVorläufige Mitt. [1]. (1980)

Lubosch, Winfried ; Seebach, Dieter

New York, NY : Wiley-Blackwell

Helvetica Chimica Acta 63 (1980), S. 102-116

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ISSN: 0018-019X

Keywords: Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: Nucleophilic Aminoalkylation with ThiopivalamidesVorläufige Mitt. [1].Of the twelve thioamides 7a-e and 8a-g, only N,N-dimethylthiopivalamide (7a) could be metallated at the CH-group in a-position to the N-Atom. The reagent 9 thus obtained (Table 1) reacts in high yields with primary haloalkanes, with aldehydes, and with non-enolizable ketones (Table 2). As shown in Scheme 1, the products can be hydrolyzed to pivalamides, cleaved to secondary amines, or reduced to neopentylamines (see 18/19, 15/equation (4) and (5), and 16/20, respectively).

Additional Material: 2 Tab.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/hlca.19800630111

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9

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Laser Induced Excitation Spectra of the Cations of Some Fluoro-substituted Phenols (B̃2 A″ ↔ X̃2 A″) in the Gaseous Phase (1980)

Maier, J. P. ; Misev, L. ; Shiley, R. H.

New York, NY : Wiley-Blackwell

Helvetica Chimica Acta 63 (1980), S. 1920-1925

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ISSN: 0018-019X

Keywords: Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: Excitation spectra of the cations of pentafluorophenol, 2,3,4-trifluorophenol, 2,4,5-trifluorophenol, 2,5-difluorophenol and 3,5-difluorophenol have been obtained by pumping the B̃2 A″ ← X̃2A″ transition with a dye laser. The cations were first produced in their ground states by Penning ionisation using argon metastables. Vibrational frequencies of some of the fundamentals have been inferred for these cations in the B̃2 A″ state from the excitation spectra, and in the X̃2 A″ state from the emission spectra. Possible applications of the reported results are suggested.

Additional Material: 3 Ill.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/hlca.19800630719

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10

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Synthesen von polyhalogenierten Butyrylchloriden, Vorläufern der pyrethroiden Haloketene1. Mitteilung über Cu+-katalysierte Radikaladditionen von Polyhalogenverbindungen an Olefine.Auszugsweise präsentiert am ‘International Symposium on Chemistry of the Pyrethroids’ vom 16.-19. Juli 1979 in Oxford, am ‘1st European Symposium on Organic Chemistry’ vom 20.-23. August 1979 in Köln, am ‘178th ACS National Meeting’ vom 9.-14. September 1979 in Washington, D.C., sowie an der Herbstversammlung der Schweizerischen Chemischen Gesellschaft vom 19.-20. Oktober 1979 in Bern. (1980)

Martin, Pierre ; Steiner, Eginhard ; Belluš, Daniel

New York, NY : Wiley-Blackwell

Helvetica Chimica Acta 63 (1980), S. 1947-1957

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ISSN: 0018-019X

Keywords: Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: Synthesis of Polyhalogenated Butyryl Chlorides, Precursors of Pyrethroid HaloketenesThe copper (I)-catalyzed free radical addition of halomethanes to acrylates and the addition of halogenated acetic acid derivatives to fluoro- or chloro-substituted ethylenes affords polyhalogenated butyric acid derivatives. Chlorides of these acids serve as precursors for haloketenes used in efficient syntheses of pyrethroids.

Additional Material: 3 Tab.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/hlca.19800630722

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