Organolithium-induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridines
The alkylative double ring-opening of Bus-protected 2,5-dihydropyrrole epoxides 13 and 29 with organolithiums to give 3-substituted 1-aminobut-3-en-2-ols 13-19 and 30-32 are described. Bus-protected tetrahydropyridine epoxide 38 reacts with organolithiums to give 4-substituted 1-aminobut-4-en-3-ols...
| المؤلفون الرئيسيون: | , , |
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| التنسيق: | Journal article |
| اللغة: | English |
| منشور في: |
2003
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| _version_ | 1826274077223944192 |
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| author | Hodgson, D Miles, T Witherington, J |
| author_facet | Hodgson, D Miles, T Witherington, J |
| author_sort | Hodgson, D |
| collection | OXFORD |
| description | The alkylative double ring-opening of Bus-protected 2,5-dihydropyrrole epoxides 13 and 29 with organolithiums to give 3-substituted 1-aminobut-3-en-2-ols 13-19 and 30-32 are described. Bus-protected tetrahydropyridine epoxide 38 reacts with organolithiums to give 4-substituted 1-aminobut-4-en-3-ols 39 and tetrahydropyridinol 40. © 2003 Elsevier Ltd. All rights reserved. |
| first_indexed | 2024-03-06T22:37:57Z |
| format | Journal article |
| id | oxford-uuid:5a91d416-25d3-4350-b533-44a6177c1277 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-06T22:37:57Z |
| publishDate | 2003 |
| record_format | dspace |
| spelling | oxford-uuid:5a91d416-25d3-4350-b533-44a6177c12772022-03-26T17:16:29ZOrganolithium-induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridinesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:5a91d416-25d3-4350-b533-44a6177c1277EnglishSymplectic Elements at Oxford2003Hodgson, DMiles, TWitherington, JThe alkylative double ring-opening of Bus-protected 2,5-dihydropyrrole epoxides 13 and 29 with organolithiums to give 3-substituted 1-aminobut-3-en-2-ols 13-19 and 30-32 are described. Bus-protected tetrahydropyridine epoxide 38 reacts with organolithiums to give 4-substituted 1-aminobut-4-en-3-ols 39 and tetrahydropyridinol 40. © 2003 Elsevier Ltd. All rights reserved. |
| spellingShingle | Hodgson, D Miles, T Witherington, J Organolithium-induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridines |
| title | Organolithium-induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridines |
| title_full | Organolithium-induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridines |
| title_fullStr | Organolithium-induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridines |
| title_full_unstemmed | Organolithium-induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridines |
| title_short | Organolithium-induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridines |
| title_sort | organolithium induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridines |
| work_keys_str_mv | AT hodgsond organolithiuminducedsynthesisofacyclicunsaturatedaminoalcoholsfromepoxidesofdihydropyrrolesandtetrahydropyridines AT milest organolithiuminducedsynthesisofacyclicunsaturatedaminoalcoholsfromepoxidesofdihydropyrrolesandtetrahydropyridines AT witheringtonj organolithiuminducedsynthesisofacyclicunsaturatedaminoalcoholsfromepoxidesofdihydropyrrolesandtetrahydropyridines |