Laburnine
Reference standards.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to
24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
Biomed Pharmacother.2024, 173:116319.
J.Pharm. & Biome. Anal.2023, 2: 100018.
Vet World.2023, 16(3):618-630.
FEMS Microbiol Lett.2017, 364(11)
Int J Mol Sci.2022, 23(23):14545.
Pharmaceuticals.2022, 15(4), 402.
Food Bioscience2024, 58:103691.
Metabolites.2020, 10(12):497.
Heliyon.2023, 9(6):e16138.
Nutrients.2020, 12(11):3448.
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J Org Chem. 1999 Apr 30;64(9):3122-3131.
Enamino Ester Reduction: A Short Enantioselective Route to Pyrrolizidine and Indolizidine Alkaloids. Synthesis of (+)-Laburnine, (+)-Tashiromine, and (-)-Isoretronecanol.[Pubmed:
11674411]
METHODS AND RESULTS:
The scope of these reductions has been extended to the synthesis of three pyrrolizidine or indolizidine alkaloids: (+)-tashiromine, (+)-Laburnine, and (-)-isoretronecanol.
CONCLUSIONS:
Syntheses of these natural products, starting from chiral beta-enamino diesters, were achieved in a short and convenient manner, leading to enantiopure compounds in good overall yields.
