Tetrahedron Letters
ISSN: 0040-4039
Datasets associated with articles published in Tetrahedron Letters
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- Data for: Spectrophotometric Determination of α-Hydroxytropolone pKa Values: A Structure-Acidity Relationship StudyUV-Vis spectra data used in the determination of pKa values of several functionalized hydroxytropolones.
- Data for: Practical enantioselective synthesis of (3S, 4R)-3-hydroxypiperidine-4-carboxylic acidSupplemental Information for enantioselective piperidine synthesis
- 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
- Data for: Two new quinolone alkaloids from Dianthus superbus var. superbusThe raw processed NMR data for the new compounds
- Data for: Synthesis of the Trisaccharide Repeating Unit of Capsular Polysaccharide from Klebsiella PneumoniaeSynthesis of the Trisaccharide Repeating Unit of Capsular Polysaccharide from Klebsiella Pneumoniae
- 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
- 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.
- 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
- 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.
- 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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