1184872-64-7Relevant academic research and scientific papers
Combining Electronic and Steric Effects to Generate Hindered Propargylic Alcohols in High Enantiomeric Excess
Vyas, Vijyesh K.,Knighton, Richard C.,Bhanage, Bhalchandra M.,Wills, Martin
supporting information, p. 975 - 978 (2018/02/23)
Tethered ruthenium-TsDPEN complexes have been applied to the catalysis of the asymmetric transfer hydrogenation of a range of aryl/acetylenic ketones. The introduction of an ortho- substituent to the aryl ring of the substrate results in a reversal of the
P(PhCH2NCH2CH2)3N: An efficient Lewis base catalyst for the synthesis of propargylic alcohols and Morita-Baylis-Hillman adducts via aldehyde alkynylation
Wadhwa, Kuldeep,Chintareddy, Venkat Reddy,Verkade, John G.
supporting information; experimental part, p. 6681 - 6690 (2009/12/30)
(Chemical Equation Presented) Proazaphosphatrane P(PhCH2NCH 2CH2)3N (1a) is an efficient catalyst for the addition of aryl trimethylsilyl alkynes to a variety of aromatic, aliphatic, and heterocyclic aldehydes i
