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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Main Authors: Adolfo Sánchez, Manuel Nogueras, Sofía Salido, Concepción Badía, Joaquín Altarejos, Pablo J. Linares-Palomino, Laura Chapado
Format: Article
Language:English
Published: MDPI AG 2009-07-01
Series:Molecules
Subjects:
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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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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