5216-82-0Relevant academic research and scientific papers
A novel and efficient direct aldol condensation from ketones and aromatic aldehydes catalyzed by proline-TEA through a new pathway
Wang, Jun-feng,Lei, Meng,Li, Qin,Ge, Ze-mei,Wang, Xin,Li, Run-tao
experimental part, p. 4826 - 4833 (2009/10/02)
A novel and efficient direct aldol condensation from various ketones and a wide range of aldehydes was catalyzed by l-proline-TEA (triethylamine) in MeOH at room temperature, affording the corresponding (E)-α,β-unsaturated ketones in excellent yields. By
APPROACHES TO THE TOTAL SYNTHESIS OF THE MONTANINE (AMARYLLIDACEAE) ALKALOIDS. PREPARATION OF ISOMERIC 3-ARYLOCTAHYDROINDOLES
Sanchez, Ignacio H.,Larraza, Maria Isabel,Rojas, Irma,Brena, Francisco Kuri,Flores, Humberto J.
, p. 3033 - 3039 (2007/10/02)
The preparation of various isomeric 3-arylooctahydroindoles, potential synthons for the total synthesis of the montanine-like Amaryllidaceae alkaloids, is described.
