137669-37-5Relevant academic research and scientific papers
Synthesis, olfactory evaluation, and determination of the absolute configuration of the 3,4-didehydroionone stereoisomers
Serra, Stefano,Fuganti, Claudio,Brenna, Elisabetta
, p. 1110 - 1122 (2007/10/03)
The synthesis of 3,4-didehydroionone isomers 4, (+)-6, and (-)-6 and of 3,4-didehydro-7,8-dihydroionone isomers 5, (+)-7, and (-)-7 was accomplished starting from commercially available racemic α-ionone (1). Their preparation of the racemic forms 4-7 was first achieved by mean of a number of chemo- and regioselective reactions (Schemes 1 and 2). The enantio- and diastereoselective lipase-mediated kinetic acetylation of 4-hydroxy-γ- ionone (10a/10b) provided 4-hydroxy-γ-ionone (+)-10a/(±)-10b and (+)-4-(acetyloxy)-γ-ionone ((+)12b) (Scheme 3). The latter compounds were used as starting materials to prepare the 3,4-didehydro-γ-ionones (+)- and (-)-6 and the 3,4-didehydro-7,8-dihydro-γ-ionones (+)- and (-)-7 in enantiomer-enriched form. The absolute configuration of (+)-12b was determine by chemical correlation with (+)-(6S)-γ-ionone ((+)-3) and with (-)-(6S)-α-ionone ((-)-1) therefore allowing to assign the (S)-configuration to (+)-6 and (+)-7. Olfactory evaluation of the above described 3,4-didehydroionone isomers shows a significant difference between the enantiomers and regioisomers both in fragrance feature and in detection threshold (Table).
Photooxygenation of α-Ionone and Oxygen Transfer Reactions of the Resulting Allylic Hydroperoxides
Adam, Waldemar,Griesbeck, Axel G.,Wang, Xiaoheng
, p. 193 - 198 (2007/10/02)
The photooxygenation of α-ionone (4) in different solvents leads, with higher than 90percent regioselectivity, to a mixture of two diastereomeric allylic hydroperoxides 5a and 5b (diastereomeric ratio 77:23).These compounds are transformed in the presence
