Medium ring ethers by ring expansion-ring contraction: Synthesis of lauthisan


Autoria(s): Coster, M. J.; De Voss, J. J.
Data(s)

01/01/2002

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

http://espace.library.uq.edu.au/view/UQ:61734

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