Molecular Crystals and Liquid Crystals (1969-1991) p. 43 - 53 (1974)
Update date:2022-09-26
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Gibson
Six new cholesteryl esters have been prepared from chiral alkanoic acids. Oxidation of 2(S)-methylbutanol and 2(S)-ethyl-3-methybutyraldehyde gave the corresponding butyric acids, while condensation of the tosylates of the corresponding alcohols with diethyl malonate led ultimately to the substituted hexanoic acids. 2(R)-Methylpentanoic and ( minus )-2-ethylhexanoic acids were commercially available.
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Doi:10.1016/S0040-4039(00)71969-1
(1975)Doi:10.1039/c0ob01208d
(2011)Doi:10.1021/jm00353a010
(1982)Doi:10.1039/c2gc35645g
(2012)Doi:10.1021/ja00016a001
(1991)Doi:10.1039/P19750000825
(1975)
