Enzyme-mediated preparation of (+)- and (-)-beta-irone and (+)- and (-)-cis-gamma-irone from Irone alpha (R)

Citation
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
Citations number
29
Categorie Soggetti
Chemistry & Analysis",Chemistry
Journal title
HELVETICA CHIMICA ACTA
ISSN journal
0018019X → ACNP
Volume
84
Issue
1
Year of publication
2001
Pages
69 - 86
Database
ISI
SICI code
0018-019X(2001)84:1<69:EPO(A(>2.0.ZU;2-Q
Abstract
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.