Transesterification-based enzymatic resolutions of racemic 3-hydroxy-4-pentenylurethanes in organic solvents
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Asymmetric intramolecular amidation of N-(tert-butoxycarbonyl)-3-hydroxy-4-pentenylamine. A new entry to chiral building blocks for the synthesis of biologically active nitrogen-containing compounds
2. The shortest synthesis of optically active Geissman-Waiss lactone, a key synthetic intermediate for necine bases
3. An asymmetric total synthesis of (−)-supinidine
4. Asymmetric synthesis of 1-hydroxyindolizidines, biosynthetic precursors to the toxic indolizidine alkaloids slaframine and swainsonine
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