69803-56-1Relevant articles and documents
Dearylation of arylphosphine oxides using a sodium hydride-iodide composite
Tejo, Ciputra,Pang, Jia Hao,Ong, Derek Yiren,Oi, Miku,Uchiyama, Masanobu,Takita, Ryo,Chiba, Shunsuke
supporting information, p. 1782 - 1785 (2018/02/21)
A new protocol for the dearylation of arylphosphine oxides was developed using sodium hydride (NaH) in the presence of lithium iodide (LiI). The transient sodium phosphinite could be functionalized with a range of electrophiles in a one-pot fashion.
Characteristic odoriferous compounds of brown algae: Syntheses of possible oxidation products of (6Z,9Z,12Z,15Z)-1,6,9,12,15-heneicosapentaene and (6Z,9Z,12Z,15Z,18Z)-1,6,9,12,15,18-heneicosahexaene
Broekhof, Nico L.J.M.,Witteveen, Jan G.,Weerdt, Anton J. A. van der
, p. 436 - 442 (2007/10/02)
The unsaturated aldehydes (3Z,6Z)-3,6,11-dodecatrienal (9), (2E,4Z,7Z)-2,4,7,12-tridecatetraenal (10) and (3Z,6Z,9Z)-3,6,9,14-pentadecatetraenal (11) are expected to be products of the air oxidation of heneicosapentaene 1 and heneicosahexaene 2.The first attempts to synthesize aldehydes 9 and 11 (which failed) were based upon repeated Horner-Wittig reactions with phosphine oxide 12.In a second attempt, acetylene chemistry was applied to prepare aldehydes 9, 10 and 11.Their olfactive properties are described.