Literature DB >> 11028024

Odds and Trends: Recent Developments in the Chemistry of Odorants Note on trademarks: Words which we know or have reason to believe constitute registered trademarks (R) are designated as such. However, neither the presence nor absence of such designation should be regarded as affecting the legal status of any trademark. Note on perfume analysis: The quoted percentages of perfume raw materials in market products are rounded figures. They are often derived from area percentages from the GC (FID) analysis, and are thus subject to analytical error.

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Abstract

Fragrance chemistry is, together with the closely related area of flavor chemistry, one of the few domains, if not the only one, in which chemists can immediately experience structure-activity relationships. This review presents structure-odor correlations and olfactophore models for the main odor notes of perfumery: "fruity", "marine", "green", "floral", "spicy", "woody", "amber", and "musky". New trendsetters and so-called captive odorants of these notes are introduced, and recent activities and highlights in fragrance chemistry are summarized. The design of odorants, their chemical synthesis, and their use in modern perfumery is discussed. Our selection is guided and illustrated by creative fragrances, and features new odorants which encompassed current trends in perfumery. New odorants for grapefruit and blackcurrant, for galbanum, and leafy top notes are presented. Compounds with fashionable marine, ozonic, and aquatic facets are treated, as well as new odorants for classical lily-of-the-valley, rose, and jasmine accords. Compounds with sweet and spicy tonalities are also discussed, as are the most recent developments for woody notes such as sandalwood and vetiver. We conclude with musky and ambery odorants possessing uncommon or unusual structural features. Some odor trends and effects are illustrated by microencapsulated fragrance samples, and areas where there is need for the development of new synthetic materials and methodologies are pointed out. Thus, chemists are invited to explore fragrance chemistry and participate in the design and synthesis of new odorants. This review gives the latest state of the art of the subject.

Entities:  

Year:  2000        PMID: 11028024     DOI: 10.1002/1521-3773(20000901)39:17<2980::aid-anie2980>3.0.co;2-#

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  20 in total

1.  Optical signatures of molecular dissymmetry: combining theory with experiments to address stereochemical puzzles.

Authors:  Parag Mukhopadhyay; Peter Wipf; David N Beratan
Journal:  Acc Chem Res       Date:  2009-06-16       Impact factor: 22.384

2.  Regio- and Diastereoselective Iron-Catalyzed [4+4]-Cycloaddition of 1,3-Dienes.

Authors:  C Rose Kennedy; Hongyu Zhong; Rachel L Macaulay; Paul J Chirik
Journal:  J Am Chem Soc       Date:  2019-05-16       Impact factor: 15.419

Review 3.  Synthesis of odorants in flow and their applications in perfumery.

Authors:  Merlin Kleoff; Paul Kiler; Philipp Heretsch
Journal:  Beilstein J Org Chem       Date:  2022-06-27       Impact factor: 2.544

4.  Characterization of beta3-adrenergic receptor: determination of pharmacophore and 3D QSAR model for beta3 adrenergic receptor agonism.

Authors:  Philip Prathipati; Anil K Saxena
Journal:  J Comput Aided Mol Des       Date:  2005-02       Impact factor: 3.686

Review 5.  Ruthenium(0)-Catalyzed Cycloaddition of 1,2-Diols, Ketols, or Diones via Alcohol-Mediated Hydrogen Transfer.

Authors:  Hiroki Sato; Ben W H Turnbull; Keisuke Fukaya; Michael J Krische
Journal:  Angew Chem Int Ed Engl       Date:  2018-02-06       Impact factor: 15.336

6.  Efficient Synthesis of the Cyclopentanone Fragrances (Z)-3-(2-oxopropyl)-2-(pent-2-en-1-yl)cyclopentanone and Magnolione.

Authors:  Guojun Pan; Robert M Williams
Journal:  Tetrahedron       Date:  2014-01-14       Impact factor: 2.457

7.  Ring expansion of cyclic 1,2-diols to form medium sized rings via ruthenium catalyzed transfer hydrogenative [4+2] cycloaddition.

Authors:  Zachary A Kasun; Laina M Geary; Michael J Krische
Journal:  Chem Commun (Camb)       Date:  2014-07-18       Impact factor: 6.222

8.  Dual activities of odorants on olfactory and nuclear hormone receptors.

Authors:  Horst Pick; Sylvain Etter; Olivia Baud; Ralf Schmauder; Lorenza Bordoli; Torsten Schwede; Horst Vogel
Journal:  J Biol Chem       Date:  2009-09-01       Impact factor: 5.157

9.  A practical chemo-enzymatic approach to highly enantio-enriched 10-ethyl-7,8-dihydro-γ-ionone isomers: a method for the synthesis of 4,5-didehydro-α-ionone.

Authors:  Assem Barakat; Abdullah M Al-Majid; Yahia Nasser Mabkhot; Zeid A Al-Othman
Journal:  Int J Mol Sci       Date:  2012-05-09       Impact factor: 6.208

10.  Exchanging ligand-binding specificity between a pair of mouse olfactory receptor paralogs reveals odorant recognition principles.

Authors:  Olivia Baud; Shuguang Yuan; Luc Veya; Slawomir Filipek; Horst Vogel; Horst Pick
Journal:  Sci Rep       Date:  2015-10-09       Impact factor: 4.379

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