Asymmetric synthesis of beta-haloaryl beta-amino acid derivatives
Lithium N-benzyl-N-α-methyl-4-methoxybenzylamide may be employed as a homochiral ammonia equivalent for the synthesis of homochiral β-haloaryl β-amino acid derivatives via a strategy involving its conjugate addition to α,β-unsaturated β-haloaryl acceptors and subsequent oxidative deprotection with c...
| Glavni autori: | , , , , , , , |
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| Format: | Journal article |
| Jezik: | English |
| Izdano: |
2001
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| _version_ | 1826301587462553600 |
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| author | Bull, S Davies, S Delgado-Ballester, S Kelly, P Kotchie, L Gianotti, M Laderas, M Smith, A |
| author_facet | Bull, S Davies, S Delgado-Ballester, S Kelly, P Kotchie, L Gianotti, M Laderas, M Smith, A |
| author_sort | Bull, S |
| collection | OXFORD |
| description | Lithium N-benzyl-N-α-methyl-4-methoxybenzylamide may be employed as a homochiral ammonia equivalent for the synthesis of homochiral β-haloaryl β-amino acid derivatives via a strategy involving its conjugate addition to α,β-unsaturated β-haloaryl acceptors and subsequent oxidative deprotection with ceric ammonium nitrate. |
| first_indexed | 2024-03-07T05:34:40Z |
| format | Journal article |
| id | oxford-uuid:e379cadb-bea0-4ca8-99b0-71f9ff1fb462 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T05:34:40Z |
| publishDate | 2001 |
| record_format | dspace |
| spelling | oxford-uuid:e379cadb-bea0-4ca8-99b0-71f9ff1fb4622022-03-27T10:09:22ZAsymmetric synthesis of beta-haloaryl beta-amino acid derivativesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:e379cadb-bea0-4ca8-99b0-71f9ff1fb462EnglishSymplectic Elements at Oxford2001Bull, SDavies, SDelgado-Ballester, SKelly, PKotchie, LGianotti, MLaderas, MSmith, ALithium N-benzyl-N-α-methyl-4-methoxybenzylamide may be employed as a homochiral ammonia equivalent for the synthesis of homochiral β-haloaryl β-amino acid derivatives via a strategy involving its conjugate addition to α,β-unsaturated β-haloaryl acceptors and subsequent oxidative deprotection with ceric ammonium nitrate. |
| spellingShingle | Bull, S Davies, S Delgado-Ballester, S Kelly, P Kotchie, L Gianotti, M Laderas, M Smith, A Asymmetric synthesis of beta-haloaryl beta-amino acid derivatives |
| title | Asymmetric synthesis of beta-haloaryl beta-amino acid derivatives |
| title_full | Asymmetric synthesis of beta-haloaryl beta-amino acid derivatives |
| title_fullStr | Asymmetric synthesis of beta-haloaryl beta-amino acid derivatives |
| title_full_unstemmed | Asymmetric synthesis of beta-haloaryl beta-amino acid derivatives |
| title_short | Asymmetric synthesis of beta-haloaryl beta-amino acid derivatives |
| title_sort | asymmetric synthesis of beta haloaryl beta amino acid derivatives |
| work_keys_str_mv | AT bulls asymmetricsynthesisofbetahaloarylbetaaminoacidderivatives AT daviess asymmetricsynthesisofbetahaloarylbetaaminoacidderivatives AT delgadoballesters asymmetricsynthesisofbetahaloarylbetaaminoacidderivatives AT kellyp asymmetricsynthesisofbetahaloarylbetaaminoacidderivatives AT kotchiel asymmetricsynthesisofbetahaloarylbetaaminoacidderivatives AT gianottim asymmetricsynthesisofbetahaloarylbetaaminoacidderivatives AT laderasm asymmetricsynthesisofbetahaloarylbetaaminoacidderivatives AT smitha asymmetricsynthesisofbetahaloarylbetaaminoacidderivatives |