Tetrahedron Letters
ISSN: 0040-4039
Datasets associated with articles published in Tetrahedron Letters
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7617 results
- Data for: Re-investigating microwave-accelerated Claisen rearrangement of allyl aryl ether: scope of catalysts, solvents, temperatures, and substrates1H NMR & HRMS of compounds 5 and 6.
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- Data for: A stereoselective synthesis of (R)-5-hydroxy-3-(4-methoxyphenethyl)cyclohex-2-enone, towards total synthesis of PrelunularinA first chiral strategy for synthesis of (R)-5-hydroxy-3-(4-methoxyphenethyl) cyclohex-2-enone reported. Key transformation includes Barbier allylation, ionic hydrogenation, Jefferey reaction, Katsuki Sharpless asymmetric epoxidation, reductive opening of epoxide and ring closing metathesis
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- Data for: Cyclic dipeptides with peroxy-groups from the fruiting bodies of the edible mushroom Tricholoma matsutakeOrigin Nuclear magnetic resonance spectra of compounds 1 and 2
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- Data for: Visible light-mediated rose bengal-catalyzed oxidative radical C-H cyclization of alkyl 1,1-biaryl-2-ones: An efficient synthesis of 10-alkylphenanthren-9-ols in waterData
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- Data for: The One-Pot Synthesis of Amidonapthoquinones from AminonaphthoquinonesNMR spectra for all new compounds
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- Data for: Sex pheromone of the aerial root mealybug, Pseudococcus baliteus: a unique monoterpenoid containing an α-hydroxyketone moietyChemical data of Pseudococcus baliteus pheromone
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- Data for: 3-(Ethoxycarbonyl)-1-(5-methyl-5-(nitrosooxy)hexyl)pyridin-1-ium cation: A green alternative to tert-butyl nitrite for synthesis of nitro-group-containing arenes and drugs at room temperatureSpectra data of product are enclosed
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- Data for: Synthetic routes to treprostinil N-acyl methylsulfonamideSynthetic protocols
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- Data for: A Chemoselective Photolabile Protecting Group for Aldehydesnuclear magnetic resonance ( 1H-NMR and 13C-NMR)
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- Data for: Catalytic Removal of tert-Butyldimethylsilyl (TBS) ether by PVP-IA mild, efficient and rapid protocol the removal of alcoholic TBDMS ethers using PVP-1 as catalyst in methanol, the procedure of deprotection of various TBDMS ethers were found to be very convenient, easy work-up, high yielding. All the compounds are unambiguously characterized by spectroscopic data. The experimental procedures were fully reproducible.
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