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Bromination of α‐Benzylidene‐γ‐butyrolactone
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| Zeitschriftentitel: | Justus Liebigs Annalen der Chemie |
|---|---|
| Personen und Körperschaften: | , , , |
| In: | Justus Liebigs Annalen der Chemie, 1978, 1978, 1, S. 124-128 |
| Format: | E-Article |
| Sprache: | Englisch |
| veröffentlicht: |
Wiley
|
| Schlagwörter: |
| author_facet |
Zimmer, Hans Hillstorm, Warren W. Rothe, Johannes Schmidt, James C. Zimmer, Hans Hillstorm, Warren W. Rothe, Johannes Schmidt, James C. |
|---|---|
| author |
Zimmer, Hans Hillstorm, Warren W. Rothe, Johannes Schmidt, James C. |
| spellingShingle |
Zimmer, Hans Hillstorm, Warren W. Rothe, Johannes Schmidt, James C. Justus Liebigs Annalen der Chemie Bromination of α‐Benzylidene‐γ‐butyrolactone Colloid and Surface Chemistry Physical and Theoretical Chemistry |
| author_sort |
zimmer, hans |
| spelling |
Zimmer, Hans Hillstorm, Warren W. Rothe, Johannes Schmidt, James C. 0075-4617 Wiley Colloid and Surface Chemistry Physical and Theoretical Chemistry http://dx.doi.org/10.1002/jlac.197819780115 <jats:title>Abstract</jats:title><jats:p>The <jats:italic>N</jats:italic>‐bromosuccinimide bromination of α‐benzylidene‐γ‐butyrolactone (<jats:bold>1</jats:bold>) proceeds with allylic rearrangement to yield 3‐(α‐bromobenzyl)‐2(5<jats:italic>H</jats:italic>)‐furanone (<jats:bold>3a</jats:bold>). A number of reactions of this compound are described. Bromination of <jats:bold>1</jats:bold> with elemental bromine leads to α‐bromo‐α‐(α‐bromobenzyl)‐γ‐butyrolactone.</jats:p> Bromination of α‐Benzylidene‐γ‐butyrolactone Justus Liebigs Annalen der Chemie |
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10.1002/jlac.197819780115 |
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Wiley, 1978 |
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Wiley, 1978 |
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Justus Liebigs Annalen der Chemie |
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49 |
| title |
Bromination of α‐Benzylidene‐γ‐butyrolactone |
| title_unstemmed |
Bromination of α‐Benzylidene‐γ‐butyrolactone |
| title_full |
Bromination of α‐Benzylidene‐γ‐butyrolactone |
| title_fullStr |
Bromination of α‐Benzylidene‐γ‐butyrolactone |
| title_full_unstemmed |
Bromination of α‐Benzylidene‐γ‐butyrolactone |
| title_short |
Bromination of α‐Benzylidene‐γ‐butyrolactone |
| title_sort |
bromination of α‐benzylidene‐γ‐butyrolactone |
| topic |
Colloid and Surface Chemistry Physical and Theoretical Chemistry |
| url |
http://dx.doi.org/10.1002/jlac.197819780115 |
| publishDate |
1978 |
| physical |
124-128 |
| description |
<jats:title>Abstract</jats:title><jats:p>The <jats:italic>N</jats:italic>‐bromosuccinimide bromination of α‐benzylidene‐γ‐butyrolactone (<jats:bold>1</jats:bold>) proceeds with allylic rearrangement to yield 3‐(α‐bromobenzyl)‐2(5<jats:italic>H</jats:italic>)‐furanone (<jats:bold>3a</jats:bold>). A number of reactions of this compound are described. Bromination of <jats:bold>1</jats:bold> with elemental bromine leads to α‐bromo‐α‐(α‐bromobenzyl)‐γ‐butyrolactone.</jats:p> |
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| author | Zimmer, Hans, Hillstorm, Warren W., Rothe, Johannes, Schmidt, James C. |
| author_facet | Zimmer, Hans, Hillstorm, Warren W., Rothe, Johannes, Schmidt, James C., Zimmer, Hans, Hillstorm, Warren W., Rothe, Johannes, Schmidt, James C. |
| author_sort | zimmer, hans |
| container_issue | 1 |
| container_start_page | 124 |
| container_title | Justus Liebigs Annalen der Chemie |
| container_volume | 1978 |
| description | <jats:title>Abstract</jats:title><jats:p>The <jats:italic>N</jats:italic>‐bromosuccinimide bromination of α‐benzylidene‐γ‐butyrolactone (<jats:bold>1</jats:bold>) proceeds with allylic rearrangement to yield 3‐(α‐bromobenzyl)‐2(5<jats:italic>H</jats:italic>)‐furanone (<jats:bold>3a</jats:bold>). A number of reactions of this compound are described. Bromination of <jats:bold>1</jats:bold> with elemental bromine leads to α‐bromo‐α‐(α‐bromobenzyl)‐γ‐butyrolactone.</jats:p> |
| doi_str_mv | 10.1002/jlac.197819780115 |
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| id | ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9qbGFjLjE5NzgxOTc4MDExNQ |
| imprint | Wiley, 1978 |
| imprint_str_mv | Wiley, 1978 |
| institution | DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-D161 |
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| physical | 124-128 |
| publishDate | 1978 |
| publishDateSort | 1978 |
| publisher | Wiley |
| record_format | ai |
| recordtype | ai |
| series | Justus Liebigs Annalen der Chemie |
| source_id | 49 |
| spelling | Zimmer, Hans Hillstorm, Warren W. Rothe, Johannes Schmidt, James C. 0075-4617 Wiley Colloid and Surface Chemistry Physical and Theoretical Chemistry http://dx.doi.org/10.1002/jlac.197819780115 <jats:title>Abstract</jats:title><jats:p>The <jats:italic>N</jats:italic>‐bromosuccinimide bromination of α‐benzylidene‐γ‐butyrolactone (<jats:bold>1</jats:bold>) proceeds with allylic rearrangement to yield 3‐(α‐bromobenzyl)‐2(5<jats:italic>H</jats:italic>)‐furanone (<jats:bold>3a</jats:bold>). A number of reactions of this compound are described. Bromination of <jats:bold>1</jats:bold> with elemental bromine leads to α‐bromo‐α‐(α‐bromobenzyl)‐γ‐butyrolactone.</jats:p> Bromination of α‐Benzylidene‐γ‐butyrolactone Justus Liebigs Annalen der Chemie |
| spellingShingle | Zimmer, Hans, Hillstorm, Warren W., Rothe, Johannes, Schmidt, James C., Justus Liebigs Annalen der Chemie, Bromination of α‐Benzylidene‐γ‐butyrolactone, Colloid and Surface Chemistry, Physical and Theoretical Chemistry |
| title | Bromination of α‐Benzylidene‐γ‐butyrolactone |
| title_full | Bromination of α‐Benzylidene‐γ‐butyrolactone |
| title_fullStr | Bromination of α‐Benzylidene‐γ‐butyrolactone |
| title_full_unstemmed | Bromination of α‐Benzylidene‐γ‐butyrolactone |
| title_short | Bromination of α‐Benzylidene‐γ‐butyrolactone |
| title_sort | bromination of α‐benzylidene‐γ‐butyrolactone |
| title_unstemmed | Bromination of α‐Benzylidene‐γ‐butyrolactone |
| topic | Colloid and Surface Chemistry, Physical and Theoretical Chemistry |
| url | http://dx.doi.org/10.1002/jlac.197819780115 |