96232-73-4Relevant academic research and scientific papers
A flexible approach to hexahydronaphthalene-1-carboxylates
Li, Zhi,Alameda-Angulo, Celia,Quiclet-Sire, Béatrice,Zard, Samir Z.
experimental part, p. 9844 - 9852 (2012/02/05)
A flexible approach to hexahydronaphthalene-1-carboxylates based on the Favorskii rearrangement of 1,1-dichloro bicyclo[5.4.0]undec-5-en-2-ones has been devised. 1,1-Dichloro bicyclo[5.4.0]undec-5-en-2-ones can be prepared from readily available cyclohexa
Tin(II) chloride dihydrate reduction of β,γ-unsaturated nitro-alkenes
Das, Nalin B.,Sarma, Jadab C.,Sharma, Ram P.,Bordoloi, Manobjyoti
, p. 869 - 872 (2007/10/02)
β,γ-Unsaturated nitro-alkenes have been converted into α,β-unsaturated ketones in good yield by tin(II) chloride dihydrate in tetrahedrofuran.
SYNTHESIS OF VINYLIC LACTONES VIA PALLADIUM-CATALYZED COUPLING OF VINYLIC HALIDES OR TRIFLATES AND UNSATURATED CARBOXYLIC ACIDS
Larock, Richard C.,Leuck, David J.,Harrison, L. Wayne
, p. 6399 - 6402 (2007/10/02)
Vinylic halides or triflates react with 3-butenoic or 4-pentenoic acids in the presence of 5percent Pd(OAc)2 or Pd(dba)2, n-Bu4NCl, i-PrNEt and either acetonitrile or N,N-dimethylformamide at 80-100 deg C to afford the corresponding γ-alkenyl-γ-butyro- or
