Dimerisation and oligomerisation by dehydrogenation as a general synthetic principle (1) part I
Summary Donor or acceptor groups and particularly capto-dative substituants determine the ease of selective hydrogen abstraction but steric factors and the nature of the dehydrogenating agent influence the relative “radical scale”. This study underlines the preparative value of dehydrodimerisations....
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Naarmann, Herbert [verfasserIn] |
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| Format: |
Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
1980 |
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| Schlagwörter: |
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| Anmerkung: |
© Springer-Verlag 1980 |
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| Übergeordnetes Werk: |
Enthalten in: Polymer bulletin - Springer-Verlag, 1978, 2(1980), 6 vom: Apr., Seite 363-372 |
|---|---|
| Übergeordnetes Werk: |
volume:2 ; year:1980 ; number:6 ; month:04 ; pages:363-372 |
| Links: |
|---|
| DOI / URN: |
10.1007/BF01064366 |
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| Katalog-ID: |
OLC2042578886 |
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| 520 | |a Summary Donor or acceptor groups and particularly capto-dative substituants determine the ease of selective hydrogen abstraction but steric factors and the nature of the dehydrogenating agent influence the relative “radical scale”. This study underlines the preparative value of dehydrodimerisations. This method allows in addition the preparation of oligomers and polymers. A continuation of this work will be published in the near future. The industrial synthesis of indigo by dehydrodimerisation of oxindol is a classical example of radical $ coupling^{(10)} $ as a reaction type on which this publication focusses: | ||
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| 650 | 4 | |a Dehydrogenation | |
| 650 | 4 | |a Indigo | |
| 700 | 1 | |a Beaujean, Michel |4 aut | |
| 700 | 1 | |a Merényi, Robert |4 aut | |
| 700 | 1 | |a Viehe, Heinz Günter |4 aut | |
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10.1007/BF01064366 doi (DE-627)OLC2042578886 (DE-He213)BF01064366-p DE-627 ger DE-627 rakwb eng 540 530 660 VZ BIODIV DE-30 fid Naarmann, Herbert verfasserin aut Dimerisation and oligomerisation by dehydrogenation as a general synthetic principle (1) part I 1980 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer-Verlag 1980 Summary Donor or acceptor groups and particularly capto-dative substituants determine the ease of selective hydrogen abstraction but steric factors and the nature of the dehydrogenating agent influence the relative “radical scale”. This study underlines the preparative value of dehydrodimerisations. This method allows in addition the preparation of oligomers and polymers. A continuation of this work will be published in the near future. The industrial synthesis of indigo by dehydrodimerisation of oxindol is a classical example of radical $ coupling^{(10)} $ as a reaction type on which this publication focusses: Hydrogen Polymer Oligomer Dehydrogenation Indigo Beaujean, Michel aut Merényi, Robert aut Viehe, Heinz Günter aut Enthalten in Polymer bulletin Springer-Verlag, 1978 2(1980), 6 vom: Apr., Seite 363-372 (DE-627)129092916 (DE-600)6871-8 (DE-576)01442861X 0170-0839 nnns volume:2 year:1980 number:6 month:04 pages:363-372 https://doi.org/10.1007/BF01064366 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-BIODIV SSG-OLC-TEC SSG-OLC-PHY SSG-OLC-CHE GBV_ILN_22 GBV_ILN_23 GBV_ILN_40 GBV_ILN_65 GBV_ILN_70 GBV_ILN_95 GBV_ILN_130 GBV_ILN_2006 GBV_ILN_2018 GBV_ILN_2021 GBV_ILN_2411 GBV_ILN_4012 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4103 GBV_ILN_4319 GBV_ILN_4323 AR 2 1980 6 04 363-372 |
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10.1007/BF01064366 doi (DE-627)OLC2042578886 (DE-He213)BF01064366-p DE-627 ger DE-627 rakwb eng 540 530 660 VZ BIODIV DE-30 fid Naarmann, Herbert verfasserin aut Dimerisation and oligomerisation by dehydrogenation as a general synthetic principle (1) part I 1980 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer-Verlag 1980 Summary Donor or acceptor groups and particularly capto-dative substituants determine the ease of selective hydrogen abstraction but steric factors and the nature of the dehydrogenating agent influence the relative “radical scale”. This study underlines the preparative value of dehydrodimerisations. This method allows in addition the preparation of oligomers and polymers. A continuation of this work will be published in the near future. The industrial synthesis of indigo by dehydrodimerisation of oxindol is a classical example of radical $ coupling^{(10)} $ as a reaction type on which this publication focusses: Hydrogen Polymer Oligomer Dehydrogenation Indigo Beaujean, Michel aut Merényi, Robert aut Viehe, Heinz Günter aut Enthalten in Polymer bulletin Springer-Verlag, 1978 2(1980), 6 vom: Apr., Seite 363-372 (DE-627)129092916 (DE-600)6871-8 (DE-576)01442861X 0170-0839 nnns volume:2 year:1980 number:6 month:04 pages:363-372 https://doi.org/10.1007/BF01064366 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-BIODIV SSG-OLC-TEC SSG-OLC-PHY SSG-OLC-CHE GBV_ILN_22 GBV_ILN_23 GBV_ILN_40 GBV_ILN_65 GBV_ILN_70 GBV_ILN_95 GBV_ILN_130 GBV_ILN_2006 GBV_ILN_2018 GBV_ILN_2021 GBV_ILN_2411 GBV_ILN_4012 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4103 GBV_ILN_4319 GBV_ILN_4323 AR 2 1980 6 04 363-372 |
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10.1007/BF01064366 doi (DE-627)OLC2042578886 (DE-He213)BF01064366-p DE-627 ger DE-627 rakwb eng 540 530 660 VZ BIODIV DE-30 fid Naarmann, Herbert verfasserin aut Dimerisation and oligomerisation by dehydrogenation as a general synthetic principle (1) part I 1980 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer-Verlag 1980 Summary Donor or acceptor groups and particularly capto-dative substituants determine the ease of selective hydrogen abstraction but steric factors and the nature of the dehydrogenating agent influence the relative “radical scale”. This study underlines the preparative value of dehydrodimerisations. This method allows in addition the preparation of oligomers and polymers. A continuation of this work will be published in the near future. The industrial synthesis of indigo by dehydrodimerisation of oxindol is a classical example of radical $ coupling^{(10)} $ as a reaction type on which this publication focusses: Hydrogen Polymer Oligomer Dehydrogenation Indigo Beaujean, Michel aut Merényi, Robert aut Viehe, Heinz Günter aut Enthalten in Polymer bulletin Springer-Verlag, 1978 2(1980), 6 vom: Apr., Seite 363-372 (DE-627)129092916 (DE-600)6871-8 (DE-576)01442861X 0170-0839 nnns volume:2 year:1980 number:6 month:04 pages:363-372 https://doi.org/10.1007/BF01064366 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-BIODIV SSG-OLC-TEC SSG-OLC-PHY SSG-OLC-CHE GBV_ILN_22 GBV_ILN_23 GBV_ILN_40 GBV_ILN_65 GBV_ILN_70 GBV_ILN_95 GBV_ILN_130 GBV_ILN_2006 GBV_ILN_2018 GBV_ILN_2021 GBV_ILN_2411 GBV_ILN_4012 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4103 GBV_ILN_4319 GBV_ILN_4323 AR 2 1980 6 04 363-372 |
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10.1007/BF01064366 doi (DE-627)OLC2042578886 (DE-He213)BF01064366-p DE-627 ger DE-627 rakwb eng 540 530 660 VZ BIODIV DE-30 fid Naarmann, Herbert verfasserin aut Dimerisation and oligomerisation by dehydrogenation as a general synthetic principle (1) part I 1980 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer-Verlag 1980 Summary Donor or acceptor groups and particularly capto-dative substituants determine the ease of selective hydrogen abstraction but steric factors and the nature of the dehydrogenating agent influence the relative “radical scale”. This study underlines the preparative value of dehydrodimerisations. This method allows in addition the preparation of oligomers and polymers. A continuation of this work will be published in the near future. The industrial synthesis of indigo by dehydrodimerisation of oxindol is a classical example of radical $ coupling^{(10)} $ as a reaction type on which this publication focusses: Hydrogen Polymer Oligomer Dehydrogenation Indigo Beaujean, Michel aut Merényi, Robert aut Viehe, Heinz Günter aut Enthalten in Polymer bulletin Springer-Verlag, 1978 2(1980), 6 vom: Apr., Seite 363-372 (DE-627)129092916 (DE-600)6871-8 (DE-576)01442861X 0170-0839 nnns volume:2 year:1980 number:6 month:04 pages:363-372 https://doi.org/10.1007/BF01064366 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-BIODIV SSG-OLC-TEC SSG-OLC-PHY SSG-OLC-CHE GBV_ILN_22 GBV_ILN_23 GBV_ILN_40 GBV_ILN_65 GBV_ILN_70 GBV_ILN_95 GBV_ILN_130 GBV_ILN_2006 GBV_ILN_2018 GBV_ILN_2021 GBV_ILN_2411 GBV_ILN_4012 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4103 GBV_ILN_4319 GBV_ILN_4323 AR 2 1980 6 04 363-372 |
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10.1007/BF01064366 doi (DE-627)OLC2042578886 (DE-He213)BF01064366-p DE-627 ger DE-627 rakwb eng 540 530 660 VZ BIODIV DE-30 fid Naarmann, Herbert verfasserin aut Dimerisation and oligomerisation by dehydrogenation as a general synthetic principle (1) part I 1980 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer-Verlag 1980 Summary Donor or acceptor groups and particularly capto-dative substituants determine the ease of selective hydrogen abstraction but steric factors and the nature of the dehydrogenating agent influence the relative “radical scale”. This study underlines the preparative value of dehydrodimerisations. This method allows in addition the preparation of oligomers and polymers. A continuation of this work will be published in the near future. The industrial synthesis of indigo by dehydrodimerisation of oxindol is a classical example of radical $ coupling^{(10)} $ as a reaction type on which this publication focusses: Hydrogen Polymer Oligomer Dehydrogenation Indigo Beaujean, Michel aut Merényi, Robert aut Viehe, Heinz Günter aut Enthalten in Polymer bulletin Springer-Verlag, 1978 2(1980), 6 vom: Apr., Seite 363-372 (DE-627)129092916 (DE-600)6871-8 (DE-576)01442861X 0170-0839 nnns volume:2 year:1980 number:6 month:04 pages:363-372 https://doi.org/10.1007/BF01064366 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-BIODIV SSG-OLC-TEC SSG-OLC-PHY SSG-OLC-CHE GBV_ILN_22 GBV_ILN_23 GBV_ILN_40 GBV_ILN_65 GBV_ILN_70 GBV_ILN_95 GBV_ILN_130 GBV_ILN_2006 GBV_ILN_2018 GBV_ILN_2021 GBV_ILN_2411 GBV_ILN_4012 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4103 GBV_ILN_4319 GBV_ILN_4323 AR 2 1980 6 04 363-372 |
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Naarmann, Herbert Beaujean, Michel Merényi, Robert Viehe, Heinz Günter |
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Naarmann, Herbert |
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540 530 660 |
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dimerisation and oligomerisation by dehydrogenation as a general synthetic principle (1) part i |
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Dimerisation and oligomerisation by dehydrogenation as a general synthetic principle (1) part I |
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Summary Donor or acceptor groups and particularly capto-dative substituants determine the ease of selective hydrogen abstraction but steric factors and the nature of the dehydrogenating agent influence the relative “radical scale”. This study underlines the preparative value of dehydrodimerisations. This method allows in addition the preparation of oligomers and polymers. A continuation of this work will be published in the near future. The industrial synthesis of indigo by dehydrodimerisation of oxindol is a classical example of radical $ coupling^{(10)} $ as a reaction type on which this publication focusses: © Springer-Verlag 1980 |
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Summary Donor or acceptor groups and particularly capto-dative substituants determine the ease of selective hydrogen abstraction but steric factors and the nature of the dehydrogenating agent influence the relative “radical scale”. This study underlines the preparative value of dehydrodimerisations. This method allows in addition the preparation of oligomers and polymers. A continuation of this work will be published in the near future. The industrial synthesis of indigo by dehydrodimerisation of oxindol is a classical example of radical $ coupling^{(10)} $ as a reaction type on which this publication focusses: © Springer-Verlag 1980 |
| abstract_unstemmed |
Summary Donor or acceptor groups and particularly capto-dative substituants determine the ease of selective hydrogen abstraction but steric factors and the nature of the dehydrogenating agent influence the relative “radical scale”. This study underlines the preparative value of dehydrodimerisations. This method allows in addition the preparation of oligomers and polymers. A continuation of this work will be published in the near future. The industrial synthesis of indigo by dehydrodimerisation of oxindol is a classical example of radical $ coupling^{(10)} $ as a reaction type on which this publication focusses: © Springer-Verlag 1980 |
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Dimerisation and oligomerisation by dehydrogenation as a general synthetic principle (1) part I |
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