Medium ring ethers by ring expansion-ring contraction: Synthesis of lauthisan
Data(s) |
01/01/2002
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Resumo |
[GRAPHICS] A new general method for the construction of medium ring ethers has been developed. This involves the ring expansion of halo-O,S-acetals followed by a Ramburg-Backlund ring contraction reaction with concomitant extrusion of the sulfur atom. This methodology has been utilized for the synthesis of cis- and trans-lauthisan. |
Identificador | |
Idioma(s) |
eng |
Publicador |
American Chemical Society |
Palavras-Chave | #Chemistry, Organic #Cis-2-ethyl-8-formyl-3,4,7,8-dihydro-2h-oxocin-3-one 3-ethylene Acetal #8-membered Cyclic Ethers #Enantioselective Synthesis #Brevetoxin-b #(+)-laurencin #Construction #Thionolactones #(+)-lauthisan #Cyclizations #Acetylene #C1 #250301 Organic Chemical Synthesis #780103 Chemical sciences |
Tipo |
Journal Article |