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1. |
Anil‐Synthese. 10. Mitteilung. Über die Darstellung von Styryl‐Derivaten des Dibenzofurans |
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Helvetica Chimica Acta,
Volume 57,
Issue 4,
1974,
Page 945-979
Jacques Garmatter,
Adolf Emil Siegrist,
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摘要:
AbstractSchiff'sche Basen des Dibenzofuran‐2‐ bzw. ‐3‐carbaldehydes mitp‐Chloranilin können mitp‐tolyl‐substituierten heterocyclischen und carbocyclischen Aromaten in Gegenwart von Dimethylformamid und Kaliumhydroxid bzw. Kalium‐t‐butylat in die entsprechenden Styryl‐Derivate übergeführt werden (« Anil‐Synthese »).Die Lage der Absorptions‐ und Fluoreszenz‐Maxima der dargestellten Grundkörper mit dem Dibenzofuran‐3‐yl‐Rest wird mit der analoger Verbindunge
ISSN:0018-019X
DOI:10.1002/hlca.19740570402
出版商:WILEY‐VCH Verlag GmbH
年代:1974
数据来源: WILEY
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2. |
8‐Oxabicyclo[5.1.0]octa‐2,4‐dien, reduktive und säurekatalysierte Ringöffnung |
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Helvetica Chimica Acta,
Volume 57,
Issue 4,
1974,
Page 980-986
Peter Schiess,
Markus Wisson,
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摘要:
Abstract8‐Oxabicyclo[5.1.0]octa‐2,4‐diene (1) is obtained from cycloheptatriene with commercial 40% peracetic acid. Upon catalytic and LiAlH4reduction the allylic CO‐bond in1is cleaved. Acid catalised hydrolysis leads to a mixture of all six possible isomeric cycloheptadienediols. With BF3in the absence of water isomerization to 3,5‐cycloptadienone is
ISSN:0018-019X
DOI:10.1002/hlca.19740570403
出版商:WILEY‐VCH Verlag GmbH
年代:1974
数据来源: WILEY
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3. |
SN2 Reactions with Carboxylic Esters. Selective cleavage of methyl esters |
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Helvetica Chimica Acta,
Volume 57,
Issue 4,
1974,
Page 987-994
Paul Müller,
Bernard Siegfried,
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摘要:
AbstractSodium cyanide in hexamethylphosphoric triamide selectively cleaves methyl esters in the presence of ethyl esters with yields ofca.80%. The mechanism of the reaction has been investigated. It consists of nucleophilic displacement by cyanide of the carboxylate ion from the alcohol carbon atom (BAl2 mechanism).
ISSN:0018-019X
DOI:10.1002/hlca.19740570404
出版商:WILEY‐VCH Verlag GmbH
年代:1974
数据来源: WILEY
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4. |
Photoelectron Spectroscopy ofperi‐Amino Naphthalenes |
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Helvetica Chimica Acta,
Volume 57,
Issue 4,
1974,
Page 994-1003
John P. Maier,
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摘要:
AbstractThe He I photoelectron spectra ofperi‐amino and dimethylamino naphthalenes are presented. The differences in the ionization energies of the π‐bands are interpreted by separation of the perturbation of the amino substituent into an inductive destabilization and conjugative stabilization. This affords the assignment of the photoelectron bands of ionization energies below 11 eV and an estimation of the dihedral angle in theperi‐dimethylamino derivatives. The data on theperi‐amino naphthalenes indicate some angular distortion in contrast to 2‐aminon
ISSN:0018-019X
DOI:10.1002/hlca.19740570405
出版商:WILEY‐VCH Verlag GmbH
年代:1974
数据来源: WILEY
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5. |
3‐C‐Hydroxymethyl‐D‐riburonic Acid Synthesis of the Branched‐Chain Uronic Acid and comparison with a carbohydrate component of a naturally occurring bilirubin conjugate |
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Helvetica Chimica Acta,
Volume 57,
Issue 4,
1974,
Page 1003-1009
Walter P. Blackstock,
Clive C. Kuenzle,
Conrad H. Eugster,
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摘要:
AbstractA novel carbohydrate has previously been isolated from human bile as a complex glycoside of bilirubin [1]. This compound has been tentatively identified as 3‐C‐hydroxymethyl‐D‐riburonic acid. To test this structural assignment the proposed branched‐chain uronic acid was synthesized. Gas chromatographic and mass spectrometric comparison of the natural and synthetic materials indicated that the proposed structure, 3‐C‐hydroxymethyl‐D‐riburonic acid, did not apply to th
ISSN:0018-019X
DOI:10.1002/hlca.19740570406
出版商:WILEY‐VCH Verlag GmbH
年代:1974
数据来源: WILEY
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6. |
Darstellung und Hydrolyse von Poly(dimethylsilyl)benzolen: Benzo[c][1,2,5]oxadisilole |
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Helvetica Chimica Acta,
Volume 57,
Issue 4,
1974,
Page 1010-1015
Walter Fink,
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摘要:
AbstractPoly(dimethylsilyl)benzenes have been prepared by ‘in situ’ reactions of polybromobenzenes with magnesium and dimethylchlorosilane in tetrahydrofuran. The hydrolysis of these compounds yields benzo[c][1,2,5]oxadisilo
ISSN:0018-019X
DOI:10.1002/hlca.19740570407
出版商:WILEY‐VCH Verlag GmbH
年代:1974
数据来源: WILEY
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7. |
The stereochemistry of fragmentation products formed in the lead tetraacetate and related oxidations of alcohols. Part. I. β‐fragmentation ofcis‐andtrans‐4‐t‐Butylcyclohexanemethanol |
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Helvetica Chimica Acta,
Volume 57,
Issue 4,
1974,
Page 1015-1035
Mihailo Lj. Mihailovič,
Jovan Bošnjak,
Živorad Čeković,
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摘要:
AbstractThe stereochemistry of β‐fragmentation products formed in the oxidation ofcis‐andtrans‐4‐t‐butylcyclohexaanemethanol with lead tetraacetate and with lead tetraacetate‐metal chloride combinations, under various reaction conditions, has been investigated, and the results compared with those obtained, under similar conditions, in the oxidative decarboxylation ofcis‐andtrans‐4‐t‐butylcyclohexanecarboxylic acid with the same reagents. It was found that all four substrates afford, under comparable conditions, identicalcis‐transproportions of the respective fragmentation products, and that, therefore, so far as steric course is concerned, both the initial homolytic and subsequent heterolytic processes involved in the lead tetraacetate fragmentation reaction are independent of the nature and configuration of
ISSN:0018-019X
DOI:10.1002/hlca.19740570408
出版商:WILEY‐VCH Verlag GmbH
年代:1974
数据来源: WILEY
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8. |
Metal Complexes with Macrocyclic Ligands, IV. Synthesis, Properties and Kinetics of Complexation with Three N‐methyl Substituted 1,4,8,11‐tetraazacyclotetradecanes |
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Helvetica Chimica Acta,
Volume 57,
Issue 4,
1974,
Page 1035-1042
Rudolf Buxtorf,
Thomas A. Kaden,
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摘要:
AbstractThe synthesis, properties and complexation of 1‐methyl‐1,4,8,11‐tetraazacyclotetradecane (1‐MeCyclam‐14), 1,5‐dimethyl‐1,5,8,12‐tetraazacyclotetradecane (2‐MeCyclam‐14) and 1,4,8,11‐tetramethyl‐1,4,8,11‐tetraazacyclotetradecane (4‐MeCyclam‐14) are described.While the Ni2+and Cu2+complexes of 1‐MeCyclam‐14 and 2‐MeCyclam‐14 exhibit square planar geometries, 4‐MeCyclam‐14 forms Ni2+and Cu2+complexes, whose absorption spectra are best explained by assuming pentaco‐ordination of the metal ions.The complexation rate of the three N‐methyl substituted macrocycles with Cu2+and Ni2+is slower than can be accounted for by water exchange and little affected by introducing methyl groups at the nitrogens. Both results are in contrast to what is known for open chain amine ligands. A mechanism for the complexation is proposed, which also explains why the products of the reaction of 4‐MeC
ISSN:0018-019X
DOI:10.1002/hlca.19740570409
出版商:WILEY‐VCH Verlag GmbH
年代:1974
数据来源: WILEY
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9. |
Notiz zur Darstellung von N‐Trimethylsilylmethyl‐glycin und einiger seiner Derivate |
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Helvetica Chimica Acta,
Volume 57,
Issue 4,
1974,
Page 1042-1044
Walter Fink,
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摘要:
AbstractEs wird eine einfache Darstellung von N‐Trimethylsilylmethyl‐glycin durch Hydrolyse von N‐Trimethylsilylmethyl‐glycinamid besc
ISSN:0018-019X
DOI:10.1002/hlca.19740570410
出版商:WILEY‐VCH Verlag GmbH
年代:1974
数据来源: WILEY
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10. |
Steroide und Sexualhormone. 251.Mitteilung [1]. Synthetische Versuche in der Limoninreihe I. Die Darstellung von C(19)‐oxygenierten 4,4‐Dimethyl‐5α‐bzw.‐5β‐steroiden |
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Helvetica Chimica Acta,
Volume 57,
Issue 4,
1974,
Page 1044-1055
Hans‐Rudolf Schlatter,
Christoph Lüthy,
Walter Graf,
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摘要:
AbstractStarting from 19‐hydroxytestosteroneacetate (1) a high yield preparation of 3‐oxo‐4,4‐dimethyl‐19‐hydroxy‐5α‐steroids (e.g.7, 9, 13and
ISSN:0018-019X
DOI:10.1002/hlca.19740570411
出版商:WILEY‐VCH Verlag GmbH
年代:1974
数据来源: WILEY
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