108644-01-5Relevant articles and documents
Efficient Trapping of Ketone Enolates with Acrylate and β-Sulfonylacrylate Thioesters, β-Sulfonyl-, β-sulfinyl- and β-Chloro-vinyl Ketones; Facile Preparation of a Hydrindanone, cis-Dimethyloctalone, and Unsaturated 1,5-Dicarbonyl Compounds
Dancer, Robert J.,Haynes, Richard K.,Laughlin, Wendy A.,Vonwiller, Simone C.
, p. 1375 - 1389 (2007/10/02)
Tandem conjugate addition-ring closure involving reaction of the lithium enolate arising from conjugate addition of lithiated (E)-but-2-enyldiphenylphosphine oxide to 2-methyl-cyclopent-2-enone with two moles of t-butylthioacrylate generates a hydrindanol
Use of β-Sulfonyl Vinyl Ketones as Equivalents to Vinyl Ketones in Robinson Annelation. Convergent, Highly Stereoselective Preparation of a Hydrindanol Related to Vitamin D from 2-Methylcyclopent-2-enone and Lithiated (E)-But-2-enyldiphenylphosphine Oxide
Haynes, Richard K.,Vonwiller, Simone C.,Hambley, Trevor W.
, p. 5162 - 5170 (2007/10/02)
Conjugate addition of lithiated (E)-but-2-enyldiphenylphosphine oxide (3) to 2-methylcyclopent-2-enone (2) in tetrahydrofuran at -20 deg C generates the enolate 8, which reacts rapidly with a series of β-sulfonyl vinyl ketones to generate unsaturated dike