61248-51-9Relevant articles and documents
Construction of trans-Ring-fused Compounds by Radical Cyclization
Clive, Derrick L. J.,Manning, Hartford W.,Boivin, Taryn L. B.
, p. 972 - 974 (1990)
Enolates derived from bicyclic lactones of type (4) are alkylated with prop-2-ynylic (and allylic) bromides to give products (5) in which the unsaturated alkyl group is syn to the remaining ring-fusion hydrogen; prop-2-ynylic aldehydes can be used instead
A synthetic approach to perhydro-3-isoquinolinones bearing an angular methyl group via organocuprate addition
Stanetty, Peter,Bahardoust, M. Hassan,Mihovilovic, Marko D.,Mereiter, Kurt
, p. 1257 - 1268 (2007/10/03)
The addition of organocuprates to the activated C-C double bond in 2H-3,3a,4,5,6,7-hexahydro-2-indenone followed by trapping of the anionic intermediate with Mel as electrophile is reported. Structural assignment of the resulting product was carried out v
Formation of trans Ring-Fused Compounds by an Alkylation-Radical Cyclization Sequence
Clive, Derrick L. J.,Manning, Hartford W.,Boivin, Taryn L. B.,Postema, Maarten H. D.
, p. 6857 - 6873 (2007/10/02)
Enolates derived from bicyclic lactones of type 1 (Scheme I) can be alkylated with 2-propynylic halides to give products 2, in which the unsaturated alkyl group is syn to the adjacent ring-fusion hydrogen.Reaction of 2 with sodium phenyl selenide and then