137513-37-2Relevant academic research and scientific papers
Preparation of oxetanes by 4-endo trig electrophilic cyclisations of cinnamic alcohols
Albert, Sébastien,Robin, Sylvie,Rousseau, Gérard
, p. 2477 - 2479 (2007/10/03)
The reaction of substituted cinnamic alcohols with bis(sym-collidine)bromine(I) hexafluorophosphate was examined. In general no oxetane was obtained when a substituent was fixed on the carbon-carbon double bond. However, oxetanes were formed in high yield
Carbon-carbon bond formation by intermolecular radical reaction. Sml2-promoted carbonyl-alkyne reductive coupling
Inanaga, Junji,Katsuki, Junko,Ujikawa, Osamu,Yamaguchi, Masaru
, p. 4921 - 4924 (2007/10/02)
An efficient intermolecular carbonyl-alkyne reductive coupling reaction was realized for the first time by using the system, Sml2-HMPA-hydrogen donor, to give the corresponding allylic alcohols in good yields.
