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Performic Acid–Sulfuric Acid System as a Key Reagent for the Synthesis of Allobetulone A-seco-derivatives.
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- Russian Journal of General Chemistry, 2024, v. 94, n. 9, p. 2277, doi. 10.1134/S1070363224090081
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- Article
In silico Assessment of Biological Activity and Ozonolytic Synthesis of Platanic Acid and Its Derived N-Acylhydrazones.
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- Russian Journal of General Chemistry, 2023, v. 93, p. S124, doi. 10.1134/S1070363223140232
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- Article
Single-Pot Ozonolytic Synthesis of Acylhydrazones from 1,1-Dichloro-2-ethenyl-2-methylcyclopropane.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 4, p. 743, doi. 10.1134/S1070363221040265
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- Article
Synthesis of Isonicotinic and Salicylic Acids Derivatives from (–)-α-Pinene and (+)-Δ3-Carene.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 11, p. 2038, doi. 10.1134/S1070363220110031
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- Article
Efficient Synthesis of Optically Pure Mono- and Binuclear Macrocyclic Polylactones from Castor Oil and Sebacic Acid.
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- Doklady Chemistry, 2023, v. 513, n. 1, p. 315, doi. 10.1134/S0012500823601031
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- Article
New Method for the Synthesis of Phenylglyoxal Derivatives.
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- Doklady Chemistry, 2022, v. 504, n. 1, p. 74, doi. 10.1134/S0012500822600109
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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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- Article
Chemiluminescence as a base for a new approach to the study of pharmacologically promising peroxide agents.
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- Doklady Chemistry, 2011, v. 436, n. 2, p. 34, doi. 10.1134/S0012500811010022
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- Article
MOLECULAR AND CRYSTAL STRUCTURES OF 2,17β-DICYANO-3,4-SECO-4(23),20(29)-LUPADIEN.
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- Journal of Structural Chemistry, 2022, v. 63, n. 12, p. 1938, doi. 10.1134/S0022476622120046
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- Article
Synthesis and Pharmacological Properties of 9-Oxo-2E-decenoic Acid.
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- Pharmaceutical Chemistry Journal, 2003, v. 37, n. 6, p. 309, doi. 10.1023/A:1026053814913
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- Article
Low-temperature hydride reduction of (3 R)-carvomentholactone.
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- Chemistry of Natural Compounds, 2012, v. 47, n. 6, p. 896, doi. 10.1007/s10600-012-0098-3
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- Article
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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- Article
Synthesis from l-menthol of optically active macroheterocycles containing ester, azine, or hydrazide groups.
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- Chemistry of Natural Compounds, 2011, v. 47, n. 2, p. 206, doi. 10.1007/s10600-011-9883-7
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- Article
Synthesis from (+)-α-pinene of optically active macrocycles containing cyclobutane, ester, azine, or hydrazide groups.
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- Chemistry of Natural Compounds, 2011, v. 47, n. 2, p. 210, doi. 10.1007/s10600-011-9884-6
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- Article
( R)-4-menthen-3-one in the synthesis of (3 S)-methylundecand (2 S)-methyldec-1-ylbromides, key synthons for ( S, S, S)-diprionylacetate.
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- Chemistry of Natural Compounds, 2010, v. 46, n. 3, p. 370, doi. 10.1007/s10600-010-9619-0
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- Article
Synthesis of symmetric macrocyclic diesterdihyrazides using successive [2+1]- and [1+1]-condensations.
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- Chemistry of Natural Compounds, 2010, v. 46, n. 1, p. 10, doi. 10.1007/s10600-010-9513-9
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- Article
Prilezhaev dihydroxylation of ( R)-octadec-9 Z-en-7-0l.
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- Chemistry of Natural Compounds, 2009, v. 45, n. 5, p. 637, doi. 10.1007/s10600-009-9441-8
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- Article
Synthesis from L-menthol of optically active macrolides with N-containing (azine or hydrazide) groups.
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- Chemistry of Natural Compounds, 2009, v. 45, n. 4, p. 470, doi. 10.1007/s10600-009-9407-x
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- Article
Synthesis of macrolides with N-containing (azine or hydrazide) groups.
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- Chemistry of Natural Compounds, 2009, v. 45, n. 4, p. 465, doi. 10.1007/s10600-009-9406-y
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- Article
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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- Article
Two approaches to the synthesis of 9-oxo-and 10-hydroxy-2 E-decenoic acids, important components of queen substance and royal jelly of honeybees Apis mellifera.
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- Chemistry of Natural Compounds, 2008, v. 44, n. 1, p. 74, doi. 10.1007/s10600-008-0019-7
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- Article
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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- Article
Natural cyclic α, β-enone monoterpenoids in nucleophilic addition reactions.
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- Chemistry of Natural Compounds, 2006, v. 42, n. 4, p. 367, doi. 10.1007/s10600-006-0161-z
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- Article
Separation of a mixture of R-menth-4-en-3-one and (−)-menthone.
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- Chemistry of Natural Compounds, 2006, v. 42, n. 3, p. 362, doi. 10.1007/s10600-006-0124-4
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- Article
Synthesis of 3 S-methylundec-1-ylbromide, a key synthon in the synthesis of ( S,S,S)-diprionylacetate, from L-(-)-menthol.
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- Chemistry of Natural Compounds, 2006, v. 42, n. 1, p. 92, doi. 10.1007/s10600-006-0043-4
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- Article
Insect Pheromones Synthesized by Oxidative Transformations of Natural Monoterpenoids.
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- Chemistry of Natural Compounds, 2005, v. 41, n. 6, p. 617, doi. 10.1007/s10600-006-0001-1
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- Article
Synthesis of (3 S,6 RS)- and (3 RS,6 RS)-Analogs of Component AI of the Aonidiella aurantii Sex Pheromone by Stepwise Alkylation of Acetoacetic Ester.
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- Chemistry of Natural Compounds, 2005, v. 41, n. 6, p. 715, doi. 10.1007/s10600-006-0018-5
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- Article
L-(-)-Menthol in the Synthesis of Key Synthons for Optically Active Methyl-Branched Insect Pheromones.
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- Chemistry of Natural Compounds, 2005, v. 41, n. 6, p. 719, doi. 10.1007/s10600-006-0019-4
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- Article
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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- Article
Synthesis of Optically Pure 3 R-methylcyclopentan-1-one from L-(-)-menthol.
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- Chemistry of Natural Compounds, 2005, v. 41, n. 5, p. 549, doi. 10.1007/s10600-005-0203-y
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- Article
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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- Article
Synthesis of the racemic analog of a honeybee (Apis mellifera) breeding pheromone component.
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- Chemistry of Natural Compounds, 2004, v. 40, n. 6, p. 593, doi. 10.1007/s10600-005-0045-7
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- Article
Novel synthesis of (4R)-4-methylpentanolide from (L)-(-)-menthol.
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- Chemistry of Natural Compounds, 2004, v. 40, n. 6, p. 548, doi. 10.1007/s10600-005-0033-y
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- Article
(R)-4-Menthen-3-one anti-Oxime and Its Transformation under Beckman Rearrangement Conditions.
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- Chemistry of Natural Compounds, 2003, v. 39, n. 6, p. 569, doi. 10.1023/B:CONC.0000018111.69227.fb
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- Article
Synthesis of a Multifunctional Pheromone of the Honeybee Apis mellifera Via Condensation of 7-Oxooctanal with Malonic Acid.
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- Chemistry of Natural Compounds, 2003, v. 39, n. 1, p. 28, doi. 10.1023/A:1024172327822
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- Article
Electronic effects of conjugated enones on their reactivity in transformations of ADD<sub>N</sub> type.
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- Journal of Structural Chemistry, 2007, v. 48, n. 1, p. 46, doi. 10.1007/s10947-007-0007-y
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- Article
Chemoselective Baeyer–Villiger Oxidation of R-(+)-Camphor with Caroʼs Acid.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 9, p. 1663, doi. 10.1134/S1070428024090069
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- Article
Undec-10-enal in the Synthesis of Undec-10-enyl Undec-10-enoate and O- and N-containing Macroheterocycles.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 2, p. 206, doi. 10.1134/S1070428024020040
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- Article
Transformations of Seven-Membered Terpene Lactones toward Low-Molecular-Weight Bioregulators.
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- Russian Journal of Organic Chemistry, 2023, v. 59, n. 6, p. 935, doi. 10.1134/S1070428023060015
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- Article
Synthesis and Anticancer Activity of N-Acylhydrazones Derived from Betulin Diacetate.
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- Russian Journal of Organic Chemistry, 2023, v. 59, n. 5, p. 787, doi. 10.1134/S107042802305007X
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- Article
New Ozonolytic Synthesis of Keto Acids from 1-Alkylcycloalkenes.
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- Russian Journal of Organic Chemistry, 2022, v. 58, n. 1, p. 163, doi. 10.1134/S1070428022010237
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- Article
First Synthesis of Betulin 20-Acylhydrazones.
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- Russian Journal of Organic Chemistry, 2022, v. 58, n. 1, p. 76, doi. 10.1134/S1070428022010109
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- Article
Synthesis of [2+1] Conjugates of Betulic Acid with α,ω-Diols.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 11, p. 1861, doi. 10.1134/S1070428021110087
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- Article
Methods for Macrolactonization of Seco Acids in the Synthesis of Natural and Biologically Active Compounds.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 5, p. 679, doi. 10.1134/S1070428021050018
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- Article
Transformations of Peroxide Products of Non-1-ene Ozonolysis by the Action of Carboxylic Acid Hydrazides.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 1, p. 113, doi. 10.1134/S1070428021010164
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- Article
Synthesis of Macroheterocycles Containing Pyridine-2,6-dicarboxylic and Adipic Acid Ester and Hydrazide Fragments Starting from Tetrahydropyran.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 12, p. 2236, doi. 10.1134/S1070428020120295
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- Article
Transformations of Peroxide Ozonolysis Products of (–)-α-Pinene and (+)-3-Carene by the Action of 4-Hydroxybenzohydrazide.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 9, p. 1673, doi. 10.1134/S1070428020090274
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- Article
Influence of Some Factors on the Progress of a New Reaction in the Chemistry of Organoaluminum Compounds.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 8, p. 1353, doi. 10.1134/S1070428020080047
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- Article
Synthesis and Properties of Methyl 3,4-Epoxy-3,11-dioxo-3,4seco-18β-olean-12-ene-30-carboxylate in a New Reaction of Organoaluminium Compounds.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 2, p. 251, doi. 10.1134/S1070428020020116
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- Article
Hydrazides of Organic Acids in the Transformations of the Peroxide Products of Non-1-ene Ozonolysis.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 11, p. 1712, doi. 10.1134/S1070428019110113
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- Article