STEREOSELECTIVE SYNTHESIS OF (3R,4S)-STATINE UTILIZING THE IRON ACETYL COMPLEX [(ETA-5-C5H5)FE(CO)(PPH3)COME] AS A CHIRAL ACETATE ENOLATE EQUIVALENT
| Main Authors: | , , |
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| Format: | Journal article |
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1993
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| _version_ | 1826291290580451328 |
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| author | Cooke, J Davies, S Naylor, A |
| author_facet | Cooke, J Davies, S Naylor, A |
| author_sort | Cooke, J |
| collection | OXFORD |
| description | |
| first_indexed | 2024-03-07T02:57:13Z |
| format | Journal article |
| id | oxford-uuid:afba6816-6206-4427-a824-575c6069148a |
| institution | University of Oxford |
| last_indexed | 2024-03-07T02:57:13Z |
| publishDate | 1993 |
| record_format | dspace |
| spelling | oxford-uuid:afba6816-6206-4427-a824-575c6069148a2022-03-27T03:51:23ZSTEREOSELECTIVE SYNTHESIS OF (3R,4S)-STATINE UTILIZING THE IRON ACETYL COMPLEX [(ETA-5-C5H5)FE(CO)(PPH3)COME] AS A CHIRAL ACETATE ENOLATE EQUIVALENTJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:afba6816-6206-4427-a824-575c6069148aSymplectic Elements at Oxford1993Cooke, JDavies, SNaylor, A |
| spellingShingle | Cooke, J Davies, S Naylor, A STEREOSELECTIVE SYNTHESIS OF (3R,4S)-STATINE UTILIZING THE IRON ACETYL COMPLEX [(ETA-5-C5H5)FE(CO)(PPH3)COME] AS A CHIRAL ACETATE ENOLATE EQUIVALENT |
| title | STEREOSELECTIVE SYNTHESIS OF (3R,4S)-STATINE UTILIZING THE IRON ACETYL COMPLEX [(ETA-5-C5H5)FE(CO)(PPH3)COME] AS A CHIRAL ACETATE ENOLATE EQUIVALENT |
| title_full | STEREOSELECTIVE SYNTHESIS OF (3R,4S)-STATINE UTILIZING THE IRON ACETYL COMPLEX [(ETA-5-C5H5)FE(CO)(PPH3)COME] AS A CHIRAL ACETATE ENOLATE EQUIVALENT |
| title_fullStr | STEREOSELECTIVE SYNTHESIS OF (3R,4S)-STATINE UTILIZING THE IRON ACETYL COMPLEX [(ETA-5-C5H5)FE(CO)(PPH3)COME] AS A CHIRAL ACETATE ENOLATE EQUIVALENT |
| title_full_unstemmed | STEREOSELECTIVE SYNTHESIS OF (3R,4S)-STATINE UTILIZING THE IRON ACETYL COMPLEX [(ETA-5-C5H5)FE(CO)(PPH3)COME] AS A CHIRAL ACETATE ENOLATE EQUIVALENT |
| title_short | STEREOSELECTIVE SYNTHESIS OF (3R,4S)-STATINE UTILIZING THE IRON ACETYL COMPLEX [(ETA-5-C5H5)FE(CO)(PPH3)COME] AS A CHIRAL ACETATE ENOLATE EQUIVALENT |
| title_sort | stereoselective synthesis of 3r 4s statine utilizing the iron acetyl complex eta 5 c5h5 fe co pph3 come as a chiral acetate enolate equivalent |
| work_keys_str_mv | AT cookej stereoselectivesynthesisof3r4sstatineutilizingtheironacetylcomplexeta5c5h5fecopph3comeasachiralacetateenolateequivalent AT daviess stereoselectivesynthesisof3r4sstatineutilizingtheironacetylcomplexeta5c5h5fecopph3comeasachiralacetateenolateequivalent AT naylora stereoselectivesynthesisof3r4sstatineutilizingtheironacetylcomplexeta5c5h5fecopph3comeasachiralacetateenolateequivalent |