PALLADIUM-CATALYZED RING EXPANSION OF VINYL OXASPIROHEXANES

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Pd(0)-catalyzed ring expansion of vinyl oxaspirohexanes occurred smoothly in the presence of 1 equiv of p-nitrophenol in tetrahydrofuran, yielding initially 2-vinylcyclopentanones in high yields. However, vinyl oxaspiroheptanes failed to undergo ring expansion under the present conditions.
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Issue Date
1991-07
Language
English
Article Type
Article
Keywords

1,3-DIENE MONOEPOXIDES; EPOXIDES; ISOMERIZATION; CYCLIZATION; EQUIVALENT; MACROLIDE; ROUTE

Citation

TETRAHEDRON LETTERS, v.32, no.28, pp.3395 - 3396

ISSN
0040-4039
DOI
10.1016/S0040-4039(00)92716-3
URI
http://hdl.handle.net/10203/58340
Appears in Collection
CH-Journal Papers(저널논문)
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