850132-77-3Relevant academic research and scientific papers
A short and convenient chemical route to optically pure 2-methyl chromanmethanols. Total asymmetric synthesis of β-, γ-, and δ-tocotrienols
Couladouros, Elias A.,Moutsos, Vassilios I.,Lampropoulou, Maria,Little, James L.,Hyatt, John A.
, p. 6735 - 6741 (2008/02/11)
(Chemical Equation Presented) With use of inexpensive commercially available raw materials, chromanmethanol precursors to the natural β-, γ-, and δ-tocotrienols have been prepared in high yield. Enzymatic resolution afforded chiral chromanmethanols in high enantiomeric excess. Subsequent attachment of the farnesyl side chain was high yielding, thus allowing the preparation of asymmetric β-, γ-, and δ-tocotrienols in one final step wherein simultaneous deprotection of the phenol and removal of the sulfone group occurs. This chemistry provides the first synthesis of natural-series β-tocotrienol.
PROCESS FOR SYNTHESIZING d-TOCOTRIENOLS
-
Page/Page column 20-21, (2010/02/11)
A process of forming a d-tocotrienols from a (2S) 2-hydroxymethyl-6--hydroxy-alkylchroman compound, through reaction with a farnesy1 Grignard or sulfone compound. Various methods of making the (2S) 2-hydroxymethyl-6-hydroxy- alklychroman compound are disclosed.
