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Fragrance material review on delta-damascone.
Lalko J, Lapczynski A, McGinty D, Bhatia S, Letizia CS, Api AM. Lalko J, et al. Food Chem Toxicol. 2007;45 Suppl 1:S205-10. doi: 10.1016/j.fct.2007.09.058. Epub 2007 Sep 14. Food Chem Toxicol. 2007. PMID: 18031903 Review.
A toxicologic and dermatologic review of delta-damascone when used as a fragrance ingredient is presented....
A toxicologic and dermatologic review of delta-damascone when used as a fragrance ingredient is presented....
Synthesis and Olfactory Properties of a 6'-Silasubstituted "Spiro[4.5]-delta-Damascone".
Lovchik MA, Kraft P. Lovchik MA, et al. Chemistry. 2017 Apr 3;23(19):4590-4596. doi: 10.1002/chem.201605378. Epub 2017 Feb 8. Chemistry. 2017. PMID: 28009935
The silicon analogue of the potent spirocyclic delta-damascone odorant 6 was synthesized from allyltrichlorosilane (15) and but-2-en-1-ol (16). ...The target compound was found to be olfactorily related to the spiro[4.5]-delta-damascone lead, but appro …
The silicon analogue of the potent spirocyclic delta-damascone odorant 6 was synthesized from allyltrichlorosilane (15) and bu …
Evaluation of the antifungal activity of alpha, beta, and delta-damascone and inclusion complexes in beta-cyclodextrin against Candida spp.
de Oliveira MRC, de Lima Silva MG, Dos Santos ATL, Batista FLA, da Costa RHS, Martins AOBPB, da Cruz BG, Morais-Braga MFB, Coutinho HDM, Magalhães FEA, de Sena Junior DM, Teixeira AMR, de Menezes IRA. de Oliveira MRC, et al. Folia Microbiol (Praha). 2022 Jun;67(3):447-457. doi: 10.1007/s12223-021-00945-2. Epub 2022 Feb 3. Folia Microbiol (Praha). 2022. PMID: 35112321
This study aimed to evaluate the antifungal activity of alpha, beta, and delta-damascone and inclusion complexes with beta-cyclodextrin against different Candida spp. ...
This study aimed to evaluate the antifungal activity of alpha, beta, and delta-damascone and inclusion complexes with beta-cyc …
Selective oxidation of carotenoid-derived aroma compounds by CYP260B1 and CYP267B1 from Sorangium cellulosum So ce56.
Litzenburger M, Bernhardt R. Litzenburger M, et al. Appl Microbiol Biotechnol. 2016 May;100(10):4447-57. doi: 10.1007/s00253-015-7269-7. Epub 2016 Jan 15. Appl Microbiol Biotechnol. 2016. PMID: 26767988
Likewise, CYP260B1 performed the allylic hydroxylation of beta-damascone [(E)-1-(2,6,6-trimethylcyclohex-1-enyl)but-2-en-1-one] and delta-damascone [(E)-1-(2,6,6-trimethylcyclohex-3-enyl)but-2-en-1-one]. ...In addition, to known products, also novel products such as …
Likewise, CYP260B1 performed the allylic hydroxylation of beta-damascone [(E)-1-(2,6,6-trimethylcyclohex-1-enyl)but-2-en-1-one] and delta
Influence of the backbone structure on the release of bioactive volatiles from maleic acid-based polymer conjugates.
Berthier DL, Paret N, Trachsel A, Herrmann A. Berthier DL, et al. Bioconjug Chem. 2010 Nov 17;21(11):2000-12. doi: 10.1021/bc100223s. Epub 2010 Oct 11. Bioconjug Chem. 2010. PMID: 20936844
In the presence of a cationic surfactant, the polymer conjugates were transferred from an aqueous medium to a cotton surface. The deposition and the release of delta-damascone from the cotton surface as a function of the polymer backbone structure were measured by f …
In the presence of a cationic surfactant, the polymer conjugates were transferred from an aqueous medium to a cotton surface. The deposition …
Thioether profragrances: parameters influencing the performance of precursor-based fragrance delivery in functional perfumery.
Maddalena U, Trachsel A, Fankhauser P, Berthier DL, Benczédi D, Wang W, Xi X, Shen Y, Herrmann A. Maddalena U, et al. Chem Biodivers. 2014 Nov;11(11):1700-33. doi: 10.1002/cbdv.201400023. Chem Biodivers. 2014. PMID: 25408319
A series of thioether profragrances was prepared by reaction of different sulfanylalkanoates with delta-damascone and tested for their release efficiencies in a fabric-softener and an all-purpose cleaner application. ...Only one of the compounds evaluated in the pre …
A series of thioether profragrances was prepared by reaction of different sulfanylalkanoates with delta-damascone and tested f …
Aromatic aldols and 1,5-diketones as optimized fragrance photocages.
Griesbeck AG, Hinze O, Görner H, Huchel U, Kropf C, Sundermeier U, Gerke T. Griesbeck AG, et al. Photochem Photobiol Sci. 2012 Mar;11(3):587-92. doi: 10.1039/c2pp05286e. Epub 2012 Feb 10. Photochem Photobiol Sci. 2012. PMID: 22322868
Aldols 3a-d are easily accessible by Mukaiyama addition and are cleaved to form the substrates with high quantum yields under solar radiation. By tuning the properties of the chromophores, a series of delta-damascone cages 5 were developed that can be used for selec …
Aldols 3a-d are easily accessible by Mukaiyama addition and are cleaved to form the substrates with high quantum yields under solar radiatio …