Works matching DE "OZONOLYSIS"
Results: 525
Cytotoxic Effects of Secosterols and Their Derivatives on Several Cultured Cells.
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- Bioscience, Biotechnology & Biochemistry, 2013, v. 77, n. 3, p. 651, doi. 10.1271/bbb.120758
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Oxidative Alkene Cleavage by Chemical and Enzymatic Methods.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 17, p. 3321, doi. 10.1002/adsc.201300882
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Gamma-radiolysis and ozonolysis of polycyclic aromatic hydrocarbons (PAHs) in solution.
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- Journal of Radioanalytical & Nuclear Chemistry, 2006, v. 267, n. 3, p. 679, doi. 10.1007/s10967-006-0103-z
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A computational study of the ozonolysis of sabinene.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2019, v. 138, n. 2, p. 1, doi. 10.1007/s00214-019-2420-7
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Towards the Synthesis of 1-Deoxy-1-nitropiperidinoses.
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- Helvetica Chimica Acta, 2010, v. 93, n. 12, p. 2297, doi. 10.1002/hlca.201000326
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Transformations of (-)- α-Pinene Peroxide Ozonolysis Products by Hydrazines of HCl and HSO.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 6, p. 1020, doi. 10.1007/s10600-016-1851-9
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Ozonolysis of Methyl 3β- Hydroxyolean- 9( 11), 12( 13)- Dien- 30- Oate.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 3, p. 448, doi. 10.1007/s10600-016-1670-z
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Ozonolysis of Unsaturated Compounds in the Synthesis of Insect Pheromones and Juvenoids.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 2, p. 199, doi. 10.1007/s10600-015-1246-3
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Oxidation of Methyl 2-Cyano-3,4- seco-4(23)-Ene-Ursolate by Ozone.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 6, p. 1037, doi. 10.1007/s10600-014-1154-y
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Synthesis and NMR Spectra of New C-Modified Glycyrrhetic Acid Derivatives.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 2, p. 302, doi. 10.1007/s10600-014-0937-5
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Synthesis of Optically Active Imidazolium Ionic Liquids Based on (+)-3-Carene.
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- Chemistry of Natural Compounds, 2013, v. 48, n. 6, p. 974, doi. 10.1007/s10600-013-0442-2
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Decomposition of ozonolysis peroxide products of (+)- α- and (+)- β-pinenes in methanol by Fe(III) salts.
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- Chemistry of Natural Compounds, 2012, v. 48, n. 5, p. 791, doi. 10.1007/s10600-012-0384-0
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Ozonolysis of cyclomusalenone and its derivatives.
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- Chemistry of Natural Compounds, 2012, v. 48, n. 5, p. 816, doi. 10.1007/s10600-012-0391-1
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Modified synthesis of methyl (1 R,2 R,3 E,5 R)-3-(hydroxyimino)-5-methyl-2-(1-methylethyl)-cyclohexanecarboxylate from ( R)-4-menthen-3-one.
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- Chemistry of Natural Compounds, 2012, v. 48, n. 5, p. 789, doi. 10.1007/s10600-012-0383-1
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Facile one-pot synthesis of anisaldehyde.
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- Chemistry of Natural Compounds, 2012, v. 48, n. 4, p. 541, doi. 10.1007/s10600-012-0304-3
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New approach to the synthesis of 9-oxo-2 E-decenoic acid, a multifunctional pheromone of queen honeybee, from the telomer of butadiene and water.
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- Chemistry of Natural Compounds, 2011, v. 47, n. 5, p. 789, doi. 10.1007/s10600-011-0060-9
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Anomalous ozonolysis product of 3β,28-di- O-acetyl-29-norlupan-20-one- O-methyloxime.
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- Chemistry of Natural Compounds, 2011, v. 47, n. 5, p. 738, doi. 10.1007/s10600-011-0047-6
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Allylic oxidation of 19 β,28-epoxy-a-neo-5 β-methyl-25-nor-18 α-olean-9-ene.
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- Chemistry of Natural Compounds, 2011, v. 47, n. 4, p. 579, doi. 10.1007/s10600-011-9999-9
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Stereospecific epoxidation of an olean-18(19)-ene-type triterpenoid.
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- Chemistry of Natural Compounds, 2011, v. 46, n. 6, p. 900, doi. 10.1007/s10600-011-9778-7
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Oxidation of ursolic acid by ozone.
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- Chemistry of Natural Compounds, 2011, v. 46, n. 6, p. 897, doi. 10.1007/s10600-011-9777-8
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Effective synthesis of 2,3- seco-2,3-dicarboxyplatanic acid.
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- Chemistry of Natural Compounds, 2010, v. 46, n. 3, p. 393, doi. 10.1007/s10600-010-9626-1
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Chemoselective oxidation of oleanolic acid derivatives with ozone.
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- Chemistry of Natural Compounds, 2010, v. 46, n. 3, p. 397, doi. 10.1007/s10600-010-9627-0
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Transformations of peroxide ozonolysis products of natural olefins by N-containing organic compounds in methanol.
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- Chemistry of Natural Compounds, 2009, v. 45, n. 3, p. 318, doi. 10.1007/s10600-009-9354-6
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Ozonolysis of 11-desoxoglycyrrhetic acid and its derivatives.
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- Chemistry of Natural Compounds, 2007, v. 43, n. 5, p. 571, doi. 10.1007/s10600-007-0195-x
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Ozonolytic transformations of olefinic derivatives of L-menthol and ricinolic acid.
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- Chemistry of Natural Compounds, 2006, v. 42, n. 6, p. 631, doi. 10.1007/s10600-006-0240-1
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Structure of the minor ozonolysis product of 19 β,28-epoxy-A- neo-18 α-olean-3(5)-ene.
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- Chemistry of Natural Compounds, 2006, v. 42, n. 5, p. 618, doi. 10.1007/s10600-006-0233-0
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Novel synthesis of Planococcus citri pheromone.
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- Chemistry of Natural Compounds, 2006, v. 42, n. 2, p. 216, doi. 10.1007/s10600-006-0082-x
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Ozonolysis of Ricinolic Acid Derivatives and Transformations of the Ozonolysis Products under Barton Reaction Conditions.
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- Chemistry of Natural Compounds, 2005, v. 41, n. 6, p. 643, doi. 10.1007/s10600-006-0003-z
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Synthesis of the Promising Chiral Synthon Isopropyl-4 R-Methyl-6-Iodohexanoate from L-(-)-Menthol.
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- Chemistry of Natural Compounds, 2005, v. 41, n. 1, p. 41, doi. 10.1007/s10600-005-0070-6
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Synthesis of (4R)-Methylnonan-1-ol and (4R,8RS)-Dimethyldecanal from (S)-(+)-3,7-Dimethyl-1,6-octadiene.
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- Chemistry of Natural Compounds, 2003, v. 39, n. 1, p. 31, doi. 10.1023/A:1024124411892
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An improved synthesis of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 6, p. 638, doi. 10.1007/s10593-018-2320-0
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Synthesis of 1,3- and 1,2,3-functionalized pyrroles via Ir(I)-catalyzed vinylation of allyl alcohols.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 5, p. 526, doi. 10.1007/s10593-017-2087-8
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(OMI).
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- Arab Journal of Geographic Information Systems, 2014, v. 2, n. 2, p. 130
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- Article
Synthesis of Polyfunctional O-Containing Compounds with Acetal Fragment by Low-Temperature Ozonolysis of 1,3-Dioxepins.
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- Doklady Chemistry, 2024, v. 514, n. 2, p. 58, doi. 10.1134/S0012500824600081
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Synthesis of New Polyfunctional Cyclic Ketals Based on Substituted 4-Methylene-1,3-dioxolanes.
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- Doklady Chemistry, 2023, v. 513, n. 2, p. 393, doi. 10.1134/S0012500823601043
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- Article
New method of preparation of alkoxyacetic acids.
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- Doklady Chemistry, 2015, v. 462, n. 1, p. 127, doi. 10.1134/S0012500815050079
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Retraction.
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- Canadian Journal of Chemical Engineering, 2015, v. 93, n. 3, p. 622, doi. 10.1002/cjce.20476
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- Article
Surface Modification of Polymer Textiles by Thermally Dried Ozone.
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- Journal of Adhesion Science & Technology, 2011, v. 25, n. 15, p. 1849, doi. 10.1163/016942410X525740
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Initiation of radical polymerization with radicals produced from thermolyzed alkene ozonates.
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- Designed Monomers & Polymers, 2002, v. 5, n. 2/3, p. 233, doi. 10.1163/156855502760157953
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- Article
Effect of Relative Humidity on the Rate of New Particle Formation for Different VOCs.
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- Atmosphere, 2024, v. 15, n. 4, p. 480, doi. 10.3390/atmos15040480
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- Article
Relative Humidity Impact on Organic New Particle Formation from Ozonolysis of α- and β-Pinene at Atmospherically Relevant Mixing Ratios.
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- Atmosphere, 2023, v. 14, n. 1, p. 173, doi. 10.3390/atmos14010173
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Experimental and Theoretical Studies of Trans-2-Pentenal Atmospheric Ozonolysis.
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- Atmosphere, 2022, v. 13, n. 2, p. 291, doi. 10.3390/atmos13020291
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Novel green process to modify ABS surface before its metallization: optophysic treatment.
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- Journal of Coatings Technology & Research, 2015, v. 12, n. 2, p. 313, doi. 10.1007/s11998-014-9632-5
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Cover Feature: An Improved Stereocontrolled Access Route to Piperidine or Azepane β‐Amino Esters and Azabicyclic β‐ and γ‐Lactams; Synthesis of Novel Functionalized Azaheterocyles (28/2021).
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 28, p. 3865, doi. 10.1002/ejoc.202100733
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An Improved Stereocontrolled Access Route to Piperidine or Azepane β‐Amino Esters and Azabicyclic β‐ and γ‐Lactams; Synthesis of Novel Functionalized Azaheterocyles.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 28, p. 3874, doi. 10.1002/ejoc.202100540
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- Article
Synthesis of (+) and (‐)‐Streptomyces coelicolor Butanolide 5 (SCB‐5).
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 22, p. 3345, doi. 10.1002/ejoc.202100497
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Stereocontrolled Synthesis of Harzialactone A and Its Three Stereoisomers by Use of Standardized Polyketide Building Blocks.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 38, p. 6078, doi. 10.1002/ejoc.202001046
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Preparation of a Key Tetraene Precursor for the Synthesis of Long Acenes.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 11, p. 1658, doi. 10.1002/ejoc.201901868
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- Article
Pactamycin and Its Derivatives: Improved Synthesis Route.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 4, p. 488, doi. 10.1002/ejoc.201901747
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- Article
Regio- and Stereoselective Synthesis of Acetallic Tetrahydropyrans as Building Blocks for Natural Products Preparation, via a Tandem [4+3]-Cycloaddition/Ozonolysis Process.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 27, p. 4674, doi. 10.1002/ejoc.201600590
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- Article