Works matching IS 00093130 AND DT 2016 AND VI 52 AND IP 2
Results: 61
A Facile and Efficient Synthesis of Caeliferin a 16:0.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 199, doi. 10.1007/s10600-016-1593-8
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A New Rumenic Acid Derivative from the Roots of Cudrania tricuspidata.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 202, doi. 10.1007/s10600-016-1594-7
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Rabdosia Acids A and B: Two New Lipids from Rabdosia lophanthoides.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 205, doi. 10.1007/s10600-016-1595-6
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New Esters of Aromatic Hydroxyl Acids from Moringa oleifera Roots.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 208, doi. 10.1007/s10600-016-1596-5
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Synthesis of Spinochrome D, A Metabolite of Various Sea-Urchin Species.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 213, doi. 10.1007/s10600-016-1597-4
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Anti-Tobacco Mosaic Virus Isocoumarins from the Leaves of Nicotiana tabacum.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 218, doi. 10.1007/s10600-016-1598-3
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A New Phenolic Compound with Antifungal Activity from Viburnum fordiae.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 222, doi. 10.1007/s10600-016-1599-2
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A New Bergenin Derivative from Ardisia maclurei.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 224, doi. 10.1007/s10600-016-1600-0
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New Diorcinol J Produced by Co-Cultivation of Marine Fungi Aspergillus sulphureus and Isaria felina.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 227, doi. 10.1007/s10600-016-1601-z
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A New Azaphilone Metabolite from the Fungus Monascus ruber.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 231, doi. 10.1007/s10600-016-1602-y
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A Novel Sesquiterpene Lactone from Ixeris sonchifolia.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 234, doi. 10.1007/s10600-016-1603-x
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Synthesis and Anticonvulsant Activity of Menthyl γ-Aminobutyrate.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 237, doi. 10.1007/s10600-016-1604-9
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Stereoselective Synthesis of Carane-Type Hydroxythiols and Disulfides Based on Them.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 240, doi. 10.1007/s10600-016-1605-8
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Triterpenoids from the Roots and Stems of Rubus alceaefolius.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 248, doi. 10.1007/s10600-016-1606-7
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Synthesis and Antitumor Activity of a New Ergosterol Derivative.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 252, doi. 10.1007/s10600-016-1607-6
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Synthesis of Vinyl-Containing Lupane- and a-Secolupane-Type Triterpene Esters.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 256, doi. 10.1007/s10600-016-1608-5
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Mass Spectrometry of Self-Assembled Supramolecular Structures of Glycyrrhetic Acid with Benzimidazole.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 262, doi. 10.1007/s10600-016-1609-4
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New Kipukasin from Marine Isolate of the Fungus Aspergillus flavus.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 266, doi. 10.1007/s10600-016-1610-y
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A New Monoterpenoid Indole Alkaloid from Tabernaemontana corymbosa.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 269, doi. 10.1007/s10600-016-1611-x
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Synthesis of N-Acylamino-Acid Derivatives of Cytisine.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 272, doi. 10.1007/s10600-016-1612-9
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Synthesis of Thiourea Derivatives of the Alkaloids Anabasine, Cytisine, and d-Pseudoephedrine. Crystal Structure of N-ethyl- N-Anabasinocarbothioamide.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 276, doi. 10.1007/s10600-016-1613-8
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Oxidation of Diterpene Alkaloids by the Urea-HO Complex.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 280, doi. 10.1007/s10600-016-1614-7
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Aliphatic and Terpene Constituents of Alcea nudiflora Extracts.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 285, doi. 10.1007/s10600-016-1615-6
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Polysaccharides from the Leaves of Lonicera japonica.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 288, doi. 10.1007/s10600-016-1616-5
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Physicochemical Properties and Nutritional Composition of Black Truffles Grown in Iran.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 290, doi. 10.1007/s10600-016-1617-4
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Lipids from Serratula centauroides.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 294, doi. 10.1007/s10600-016-1618-3
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Sterols and Fatty Acids Isolated from Laboratory Culture of the Toxic Marine Diatom Pseudo-nitzschia pungens.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 296, doi. 10.1007/s10600-016-1619-2
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Phospholipids from Soft Tissues of the Bivalve Mollusk Anadara broughtonii.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 299, doi. 10.1007/s10600-016-1620-9
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Salicylic Acid Derivatives and Other Components from Gaultheria trichoclada.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 301, doi. 10.1007/s10600-016-1621-8
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Secondary Metabolites from the Endophytic Fungus Penicillium citrinum.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 304, doi. 10.1007/s10600-016-1622-7
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Flavone Di- C-Glycosides from Selaginella uncinata and Their Antioxidative Activities.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 306, doi. 10.1007/s10600-016-1623-6
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Chemical Constituents of the Flowers of Fritillaria pallidiflora.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 309, doi. 10.1007/s10600-016-1624-5
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Antibacterial and Antioxidative Compounds from Oroxylum indicum.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 311, doi. 10.1007/s10600-016-1625-4
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Chemical Constituents of Fruit Shells of Passiflora edulis.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 314, doi. 10.1007/s10600-016-1626-3
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Chemical Constituents of the Wood of Aquilaria agallocha.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 316, doi. 10.1007/s10600-016-1627-2
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Flavonoids and Sterols from Zygophyllum fabago.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 318, doi. 10.1007/s10600-016-1628-1
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Phytochemical Investigation of the Seeds of Artemisia sphaerocephala.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 320, doi. 10.1007/s10600-016-1629-0
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Method for Obtaining Total Flavonoids from Climacoptera subcrassa and Their Biological Activity.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 322, doi. 10.1007/s10600-016-1630-7
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Biologically Active Compounds from Chamaenerion angustifolium and Stachys annua Growing in Azerbaidzhan.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 324, doi. 10.1007/s10600-016-1631-6
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Biologically Active Metabolites of the Soil Actinomycetes Streptomyces ferralitis NYS57.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 326, doi. 10.1007/s10600-016-1632-5
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Phenolic Compounds from Berries of Three Vaccinium Species.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 329, doi. 10.1007/s10600-016-1633-4
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Chemical Profile and Antimicrobial Activity of Essential Oil of Piper ilheusense.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 331, doi. 10.1007/s10600-016-1634-3
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GC-MS Analysis of Essential Oil from the Flowers of Musa basjoo.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 334, doi. 10.1007/s10600-016-1635-2
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Essential Oil Composition of Dianthus jacobsii.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 336, doi. 10.1007/s10600-016-1636-1
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Volatile Constituents of the Endemic Species Platychaete glaucescens.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 338, doi. 10.1007/s10600-016-1637-0
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Chemical Composition and Antibacterial Activity of Bidens pilosa.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 340, doi. 10.1007/s10600-016-1638-z
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Essential Oil Composition of the Different Parts of Ruscus hyrcanus.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 342, doi. 10.1007/s10600-016-1639-y
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Chemical Composition of Vernonia albicans Roots from India.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 345, doi. 10.1007/s10600-016-1640-5
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Synthesis of Esters of the Monoterpene Glycoside Paeoniflorin.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 347, doi. 10.1007/s10600-016-1641-4
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A Natural-Sourced Cadinane Sesquiterpene from Inula britannica.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 2, p. 350, doi. 10.1007/s10600-016-1642-3
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