Synthesis and Olfactory Evaluation of Bulky Moiety-Modified Analogues to the Sandalwood Odorant Polysantol®
Five new bulky moiety-modified analogues of the sandalwood odorant Polysantol® have been synthesized by aldol condensation of appropriate aldehydes with butanone, deconjugative α-methylation of the resulting α,β-unsaturated ketones, and reduction of the corresponding β,γ-unsaturated ketones. The fin...
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MDPI AG
2009-07-01
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Series: | Molecules |
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Online Access: | http://www.mdpi.com/1420-3049/14/8/2780/ |
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author | Adolfo Sánchez Manuel Nogueras Sofía Salido Concepción Badía Joaquín Altarejos Pablo J. Linares-Palomino Laura Chapado |
author_facet | Adolfo Sánchez Manuel Nogueras Sofía Salido Concepción Badía Joaquín Altarejos Pablo J. Linares-Palomino Laura Chapado |
author_sort | Adolfo Sánchez |
collection | DOAJ |
description | Five new bulky moiety-modified analogues of the sandalwood odorant Polysantol® have been synthesized by aldol condensation of appropriate aldehydes with butanone, deconjugative α-methylation of the resulting α,β-unsaturated ketones, and reduction of the corresponding β,γ-unsaturated ketones. The final compounds were evaluated organoleptically and one of them seemed to be of special interest for its natural sandalwood scent. |
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format | Article |
id | doaj.art-dc7a2ea0a0824cb3bf37aceb3d9facd6 |
institution | Directory Open Access Journal |
issn | 1420-3049 |
language | English |
last_indexed | 2024-12-18T04:41:08Z |
publishDate | 2009-07-01 |
publisher | MDPI AG |
record_format | Article |
series | Molecules |
spelling | doaj.art-dc7a2ea0a0824cb3bf37aceb3d9facd62022-12-21T21:20:43ZengMDPI AGMolecules1420-30492009-07-011482780280010.3390/molecules14082780Synthesis and Olfactory Evaluation of Bulky Moiety-Modified Analogues to the Sandalwood Odorant Polysantol®Adolfo SánchezManuel NoguerasSofía SalidoConcepción BadíaJoaquín AltarejosPablo J. Linares-PalominoLaura ChapadoFive new bulky moiety-modified analogues of the sandalwood odorant Polysantol® have been synthesized by aldol condensation of appropriate aldehydes with butanone, deconjugative α-methylation of the resulting α,β-unsaturated ketones, and reduction of the corresponding β,γ-unsaturated ketones. The final compounds were evaluated organoleptically and one of them seemed to be of special interest for its natural sandalwood scent.http://www.mdpi.com/1420-3049/14/8/2780/sandalwood odorantsPolysantol® analoguesnopol derivativeodour evaluation |
spellingShingle | Adolfo Sánchez Manuel Nogueras Sofía Salido Concepción Badía Joaquín Altarejos Pablo J. Linares-Palomino Laura Chapado Synthesis and Olfactory Evaluation of Bulky Moiety-Modified Analogues to the Sandalwood Odorant Polysantol® Molecules sandalwood odorants Polysantol® analogues nopol derivative odour evaluation |
title | Synthesis and Olfactory Evaluation of Bulky Moiety-Modified Analogues to the Sandalwood Odorant Polysantol® |
title_full | Synthesis and Olfactory Evaluation of Bulky Moiety-Modified Analogues to the Sandalwood Odorant Polysantol® |
title_fullStr | Synthesis and Olfactory Evaluation of Bulky Moiety-Modified Analogues to the Sandalwood Odorant Polysantol® |
title_full_unstemmed | Synthesis and Olfactory Evaluation of Bulky Moiety-Modified Analogues to the Sandalwood Odorant Polysantol® |
title_short | Synthesis and Olfactory Evaluation of Bulky Moiety-Modified Analogues to the Sandalwood Odorant Polysantol® |
title_sort | synthesis and olfactory evaluation of bulky moiety modified analogues to the sandalwood odorant polysantol r |
topic | sandalwood odorants Polysantol® analogues nopol derivative odour evaluation |
url | http://www.mdpi.com/1420-3049/14/8/2780/ |
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