Facile preparation of methyl 5-aryl-4-hydroxyhex-2(E)-enoate, chiral synthon of bisabolane-type sesquiterpenes, based on lipase-catalyzed kinetic resolution and rearrangement of an aryl group
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
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1. Total Synthesis of (S)-(+)- and (R)-(-)-Curcudiols Based on 1,2-Aryl Migration via Phenonium Ion
2. Synthesis of (R)-Curcumene and (R)-Xanthorrizol Based on 1,2-Aryl Migration via Phenonium Ion
3. Solvolysis of (4,5)-anti-4-Aryl-5-tosyloxy-2(E)-hexenoate Derivatives
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1. Vinyl Epoxides in Organic Synthesis;Chemical Reviews;2014-04-29
2. Enantiopure 3-methyl-3,4-dihydroisocoumarins and 3-methyl-1,2,3,4-tetrahydroisoquinolines via chemoenzymatic asymmetric transformations;Catalysis Science & Technology;2012
3. Enzymatic resolution of methyl (2E, 4R*,5S*)-4-(N-benzyl-N-methyl)amino-5-hydroxyhex-2-enoate;Journal of Molecular Catalysis B: Enzymatic;2011-04
4. Natural Products Syntheses Based on the Biotransformation Using Biocatalyst;YAKUGAKU ZASSHI;2011-02-01
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