G. Brenna et al., Enzyme-mediated preparation of (+)- and (-)-beta-irone and (+)- and (-)-cis-gamma-irone from Irone alpha (R), HELV CHIM A, 84(1), 2001, pp. 69-86
The (-)- and (+)-beta -irones ((-)- and (+)-2, resp.), contaminated with ca
. 7 - 9% of the (+)- and (-)-trans-alpha -isomer, respectively, were obtain
ed from racemic alpha -irone via the 2,6-trans-epoxide (+/-)-4 (Scheme 2).
Relevant steps in the sequence were the LiAlH4 reduction of the latter, to
provide the diastereoisomeric-4,5-dihydro-5-hydroxy-trans-alpha -irols (+/-
)-6 and (+/-)-7 resolved into the enantiomers by lipase-PS-mediated acetyla
tion with vinyl acetate. The enantiomerically pure allylic acetate esters (
+)- and (-)-8 and (+)- and (-)-9, upon treatment with POCl3/pyridine, were
converted to the beta -irol acetate derivatives (+)- and (-)-10, and (+)- a
nd (-)-11, respectively, eventually providing the desired ketones (+)- and
(-)-2 by base hydrolysis and MnO2 oxidation. The 2,6-cis-epoxide (+/-)-5 pr
ovided the 4,5-dihydro-4-hydroxy-cis-alpha -irols (+/-)-13 and (+/-)14 in a
3 :1 mixture with the isomeric 5-hydroxy derivatives (+/-)-15 and (+/-)-16
on hydride treatment (Scheme 1). The POCl3/pyridine treatment of the enant
iomerically pure,allylic acetate esters, obtained by enzymic resolution of
(+/-)-13 and (+/-)-14, provided enantiomerically pure cis-alpha -irol aceta
te esters, from which ketones (+)- and (-)-22 were prepared (Scheme 4). The
same materials were obtained from the (9S) alcohols (+)-13 and (-)-14, tre
ated first with MnO2, then with POCl3/pyridine (Scheme 4). Conversely, the
dehydration with POCl3/pyridine of the enantiomerically pure 2,6-cis-5-hydr
oxy derivatives obtained from (+/-)-15 and (1)-16 gave rise to a mixture in
which the gamma -irol acetates 25a and 25b and 26a and 26b prevailed over
the alpha- and beta -isomers (Scheme,le 5). The (+)- and (-)-cis-gamma -iro
nes ((+)- and (-)-3, reap.) were obtained from the latter mixture by a sequ
ence involving as the key step the photochemical isomerization of the alpha
-double bond to the gamma -double bond. External panel olfactory evaluatio
n assigned to (+)-beta -irone ((+)-2) and to (-)-cis-gamma -irone ((-)-3) t
he strongest character and the possibility to be used as dry-down note.