Expedient Route to the functionalized calyciphylline A-type skeleton via a Michael addition-RCM strategy.
An efficient, robust, and scalable strategy to access the functionalized core of calyciphylline A-type alkaloids has been developed starting from commercially available 3-methylanisole. Key features of this approach are an intramolecular Michael addition/allylation sequence and a ring-closing metath...
| Main Authors: | , , , , |
|---|---|
| Format: | Journal article |
| Language: | English |
| Published: |
2011
|
| _version_ | 1797080426803625984 |
|---|---|
| author | Sladojevich, F Michaelides, I Benjamin, D Ward, J Dixon, D |
| author_facet | Sladojevich, F Michaelides, I Benjamin, D Ward, J Dixon, D |
| author_sort | Sladojevich, F |
| collection | OXFORD |
| description | An efficient, robust, and scalable strategy to access the functionalized core of calyciphylline A-type alkaloids has been developed starting from commercially available 3-methylanisole. Key features of this approach are an intramolecular Michael addition/allylation sequence and a ring-closing metathesis step. |
| first_indexed | 2024-03-07T00:59:52Z |
| format | Journal article |
| id | oxford-uuid:89580c4d-b77c-42ba-b72b-7a4dd1195d06 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T00:59:52Z |
| publishDate | 2011 |
| record_format | dspace |
| spelling | oxford-uuid:89580c4d-b77c-42ba-b72b-7a4dd1195d062022-03-26T22:23:57ZExpedient Route to the functionalized calyciphylline A-type skeleton via a Michael addition-RCM strategy.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:89580c4d-b77c-42ba-b72b-7a4dd1195d06EnglishSymplectic Elements at Oxford2011Sladojevich, FMichaelides, IBenjamin, DWard, JDixon, DAn efficient, robust, and scalable strategy to access the functionalized core of calyciphylline A-type alkaloids has been developed starting from commercially available 3-methylanisole. Key features of this approach are an intramolecular Michael addition/allylation sequence and a ring-closing metathesis step. |
| spellingShingle | Sladojevich, F Michaelides, I Benjamin, D Ward, J Dixon, D Expedient Route to the functionalized calyciphylline A-type skeleton via a Michael addition-RCM strategy. |
| title | Expedient Route to the functionalized calyciphylline A-type skeleton via a Michael addition-RCM strategy. |
| title_full | Expedient Route to the functionalized calyciphylline A-type skeleton via a Michael addition-RCM strategy. |
| title_fullStr | Expedient Route to the functionalized calyciphylline A-type skeleton via a Michael addition-RCM strategy. |
| title_full_unstemmed | Expedient Route to the functionalized calyciphylline A-type skeleton via a Michael addition-RCM strategy. |
| title_short | Expedient Route to the functionalized calyciphylline A-type skeleton via a Michael addition-RCM strategy. |
| title_sort | expedient route to the functionalized calyciphylline a type skeleton via a michael addition rcm strategy |
| work_keys_str_mv | AT sladojevichf expedientroutetothefunctionalizedcalyciphyllineatypeskeletonviaamichaeladditionrcmstrategy AT michaelidesi expedientroutetothefunctionalizedcalyciphyllineatypeskeletonviaamichaeladditionrcmstrategy AT benjamind expedientroutetothefunctionalizedcalyciphyllineatypeskeletonviaamichaeladditionrcmstrategy AT wardj expedientroutetothefunctionalizedcalyciphyllineatypeskeletonviaamichaeladditionrcmstrategy AT dixond expedientroutetothefunctionalizedcalyciphyllineatypeskeletonviaamichaeladditionrcmstrategy |