Approaches to diene based homopumiliotoxin alkaloids.
| Data(s) |
23/09/1996
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|---|---|
| Resumo |
<p>Palladium catalysed reductive cyclisation of a 1,1-dibromoalkene to an acetylene gives the core unit of the quinolizidine based diene homopuniliotoxin alkaloids with complete control of stereochemistry of the exocyclic double bond. Copyright (C) 1996 Elsevier Science Ltd</p> |
| Identificador | |
| Idioma(s) |
eng |
| Direitos |
info:eu-repo/semantics/restrictedAccess |
| Fonte |
McAlonan , H , Montgomery , D & Stevenson , P J 1996 , ' Approaches to diene based homopumiliotoxin alkaloids. ' Tetrahedron Letters , vol 37 , no. 39 , pp. 7151-7154 . |
| Palavras-Chave | #ENANTIOSELECTIVE TOTAL SYNTHESIS #PUMILIOTOXIN-A ALKALOIDS #CYCLIZATION #ACETYLENES #339B |
| Tipo |
article |
