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1. |
Advances in chemical studies on low‐molecular weight metabolites of marine fungi |
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Journal für Praktische Chemie/Chemiker‐Zeitung,
Volume 340,
Issue 7,
1998,
Page 589-607
M. A. Farooq Biabani,
Hartmut Laatsch,
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摘要:
AbstractThe world oceans represent a resource of huge dimension, but their microbial diversity is still poorly understood. The chemistry of marine fungi was even a widely neglected part of natural product chemistry until recently. But symbiotic and epibiotic coexistence of fungi with higher forms of life,e.g. with sponges, forming highly specialised communities gave rise to an increasing interest in their secondary metabolism. More than 100 metabolites from marine fungi are known now, many of them showing fascinating structures or remarkable biological activities. This review gives a comprehensive summary of most structures and discusses their origin and properties.
ISSN:0941-1216
DOI:10.1002/prac.19983400702
出版商:WILEY‐VCH Verlag GmbH
年代:1998
数据来源: WILEY
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2. |
Effect of Lateral Nitro Groups on the Properties of Sulfur‐Ligated Twin Mesogens |
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Journal für Praktische Chemie/Chemiker‐Zeitung,
Volume 340,
Issue 7,
1998,
Page 608-612
Amália Uamusse,
Heinz Dehne,
Helmut Reinke,
Jörgen Dobbertin,
Christoph Schick,
Siegmar Diele,
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摘要:
AbstractThe syntheses and the properties of new sulfurligated liquid crystalline sulfones, containing biphenyl units, as well as the influence of lateral nitro groups on their phase behaviour are described. Differential scanning calorimetry, optical polarizing microscopy and X‐ray diffraction measurements reveal liquid crystalline properties for most of the synthesized bis(4‐alkoxy‐biphenyl‐3‐yl)sulfones (4). The mesomorphic behaviour of these compounds is compared with that of the corresponding nitro compounds6. The bis(4‐alkoxy‐6‐nitrobiphenyl‐3‐yl)sulfones (6) are not mesogenic. The results demonstrate that lateral nitro groups introduced into the biphenyl unit, changing the length‐breadth relation, depress the thermal stability and lead to the loss of the m
ISSN:0941-1216
DOI:10.1002/prac.19983400703
出版商:WILEY‐VCH Verlag GmbH
年代:1998
数据来源: WILEY
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3. |
Synthese und spektroskopische Eigenschaften von Alkylchinolin‐8‐ol‐Extragenzien und deren Cu(II)‐, Zn(II)‐ und Cd(II)‐Komplexen |
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Journal für Praktische Chemie/Chemiker‐Zeitung,
Volume 340,
Issue 7,
1998,
Page 613-622
R. Neumann,
E. Weber,
A. Möckel,
G. Subklew,
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摘要:
Synthesis and Spectroscopic Properties of Alkylquinoline‐8‐ol Extractants and their Cu(II)‐, Zn(II)‐ and Cd(II)‐ComplexesA series of deprotonizable chelating agentsHLbeing characteristic of 2‐, 5‐ and 7‐alkyl substituted 8‐hydroxyquinolines or 5‐ and 7‐alkyl substituted 8‐hydroxyquinaldines of different alkyl chain length,H1–H5, and their Cu(II)‐, Zn(II)‐ und Cd(II)‐complexes,M(1)2–M(5)2, have been synthesized. Influences of the alkyl groups, including substituent effects on the spectroscopic properties (MS, IR, UV‐VIS,1H und13C NMR) of the free li
ISSN:0941-1216
DOI:10.1002/prac.19983400704
出版商:WILEY‐VCH Verlag GmbH
年代:1998
数据来源: WILEY
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4. |
Reaction of nitrilimines with alkoxycarbonyl‐hydrazines: Synthesis of 6‐Acetyl‐4‐aryl‐2‐ethoxycarbonyl‐1,2,3,4‐tetrahydro‐s‐tetrazines |
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Journal für Praktische Chemie/Chemiker‐Zeitung,
Volume 340,
Issue 7,
1998,
Page 623-626
Mihtab R. El‐Haddad,
Abed El‐Rahman S. Ferwanah,
Adel M. Awadallah,
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摘要:
AbstractNitrilimines2are found to react with alkoxycarbonylhydrazines3–5to afford the acyclic adducts6–8. 6cis oxidized upon heating with charcoal in refluxing toluene to the corresponding formazan9c. Compounds8cyclize upon heating with charcoal in refluxing toluene to the corresponding 6‐acetyl‐4‐aryl‐2‐ethoxycarbonyl‐1,2,3,4‐tetrahydro‐s‐tetrazines (10) rather than to the expected corresponding tetrazinones11. NMR study of compounds10showed that these compounds exist in a t
ISSN:0941-1216
DOI:10.1002/prac.19983400705
出版商:WILEY‐VCH Verlag GmbH
年代:1998
数据来源: WILEY
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5. |
Rhodium(II) acetate‐catalyzed Reaction of 2‐Amino‐4,5‐dihydro‐3‐furancarbonitriles with α‐Diazo‐β‐keto Esters |
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Journal für Praktische Chemie/Chemiker‐Zeitung,
Volume 340,
Issue 7,
1998,
Page 627-631
Kenji Yamagata,
Keiko Akizuki,
Motoyoshi Yamazaki,
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摘要:
Abstract2‐Amino‐4,5‐dihydro‐3‐furancarbonitriles (1) react with α‐diazo‐β‐keto esters in the presence of rhodium (II) acetate to give alkyl 2H‐pyran‐2‐carboxylates (2) in good yields. Benzoylation of2with benzoyl chloride provided alkyl 3‐benzoylimino‐2H‐pyran‐2‐carboxylates (4). The formation of2could be explained by a mechanism involving an oxonium ylide derived
ISSN:0941-1216
DOI:10.1002/prac.19983400706
出版商:WILEY‐VCH Verlag GmbH
年代:1998
数据来源: WILEY
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6. |
Synthesis of components for supramolecules incorporating cycloheptatriene building blocks |
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Journal für Praktische Chemie/Chemiker‐Zeitung,
Volume 340,
Issue 7,
1998,
Page 632-641
J. Neigenfink,
A. Martin,
V. Wendel,
W. Abraham,
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摘要:
AbstractMolecular threadsI–IIIincorporating 1,3,5‐cycloheptatriene units have been synthesized by three methods. Bridges were designed as ether (9,14,18and22), ester (4and14) and amino functions (25), respectively, The attachment of a second aryl residue at the seven‐membered ring by nucleophilic attack of activated aromatic compounds such as anilines on tropylium salts resulted in the formation of two regioisomers (26and27). The macrocycles28were formed under high dilution conditions in good y
ISSN:0941-1216
DOI:10.1002/prac.19983400707
出版商:WILEY‐VCH Verlag GmbH
年代:1998
数据来源: WILEY
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7. |
Bimolecular formation of radicals by hydrogen transfer. 14. The uncatalyzed Transfer Hydrogenation of α‐Methylstyrene by 2,6‐disubstituted 9,10‐Dihydroanthracenes |
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Journal für Praktische Chemie/Chemiker‐Zeitung,
Volume 340,
Issue 7,
1998,
Page 642-648
Friedrich Keller,
Christoph Rüchardt,
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摘要:
Abstract2,6‐Dimethoxy‐(4a), 2,6‐bis(dimethylamino)‐(4b), 2,6‐dichloro‐ (4c) and 2,6‐dimethoxycarbonyl‐9,10‐dihydroanthracene (4d) were prepared by conventional methods and used as hydrogen transfer donors to α‐methylstyrene (5) between 290‐350 °C. The mechanism followed second order kinetics and the rate constants were only slightly influenced by the solvent polarity and the type of substituents introduced. The activation parameters are also closely similar in the series with ΔS≠values between −21 and −28 cal/mol K. These results, together with the observation of a large isotope effect (kH/kD= 1.4–2.0 at 310–350 °C), suggest that the mechanism involves a primary kinetic H‐atom‐transfer from the donors to α‐methylstyrene (5) in the rate determining step. The compounds4a–4dconstitute a new probe for investi
ISSN:0941-1216
DOI:10.1002/prac.19983400708
出版商:WILEY‐VCH Verlag GmbH
年代:1998
数据来源: WILEY
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8. |
Synthesis of 6‐ethoxy‐6H‐1,2‐oxazines by hetero Diels‐Alder reaction of 1‐bromo‐2‐ethoxyethene with α‐nitroso alkenes |
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Journal für Praktische Chemie/Chemiker‐Zeitung,
Volume 340,
Issue 7,
1998,
Page 649-655
Kai Homann,
Jörg Angermann,
Markus Collas,
Reinhold Zimmer,
Hans‐Ulrich Reißig,
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摘要:
AbstractA variety of 6H‐1,2‐oxazines10could efficiently be prepared by hetero Diels–Alder reaction of α‐nitroso alkenes2with 1‐bromo‐2‐ethoxyethene (8) and consecutive elimination of HBr by DBU. Heterodienes2were generatedin situfrom α‐halogen oximes6. Primary cycloadducts9were isolated in singular cases, however, an attempt to substitute bromide in9eby an azido group gave the desired compound11only as minor component together with elimination product10e. 6H‐1,2‐oxazines10are valuable precursors for addition reactions which open new sy
ISSN:0941-1216
DOI:10.1002/prac.19983400709
出版商:WILEY‐VCH Verlag GmbH
年代:1998
数据来源: WILEY
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9. |
A Practical Synthesis of the Cyclohexyl Part of the Immunosuppressant FK506 |
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Journal für Praktische Chemie/Chemiker‐Zeitung,
Volume 340,
Issue 7,
1998,
Page 656-661
Bernd‐Uwe Haller,
Susanne Kruber,
Martin E. Maier,
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摘要:
AbstractStarting from the benzylidene lactone3of D‐(−)‐quinic acid the cyclohexyl fragment15(C‐28‐C‐34 part) of the immunosuppressant FK506 was synthesized. Key steps include homolytic deoxygenation reactions on compounds4and6as well as a regioselective opening of the benzylidene acetal5. Opening of the lactone7to provide the methyl ester8was followed by methylation of the hydroxy group to give9. Further steps provided the aldehyde12which was elongated to the alkyne15. This sequence provides15in gram
ISSN:0941-1216
DOI:10.1002/prac.19983400710
出版商:WILEY‐VCH Verlag GmbH
年代:1998
数据来源: WILEY
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10. |
Axial Chiral Liquid Crystals–Synthesis of Trisubstituted Allenyl Ethers |
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Journal für Praktische Chemie/Chemiker‐Zeitung,
Volume 340,
Issue 7,
1998,
Page 662-668
Ralph Lunkwitz,
Kerstin Zab,
Carsten Tschierske,
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摘要:
AbstractThe synthesis of racemic and enantiomerical enriched axial chiral liquid crystalline compounds incorporating a trisubstituted allene unit is described. All compounds16–28display the smectic C‐phase and mostly also a nematic mesophase. All investigated enantiomerically enriched compounds have a ferroelectrically switchable chiral smectic SC*‐
ISSN:0941-1216
DOI:10.1002/prac.19983400711
出版商:WILEY‐VCH Verlag GmbH
年代:1998
数据来源: WILEY
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