Spiro heterocyclic compounds. IV. Synthesis of spiro[oxindole-3,4'-(2',3'-dihydro-4'H-pyran)] and spiro[oxindole-3,4'-(1',4'-dihydropyridine)] compounds.
Author:
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb1958/28/5/28_5_1540/_pdf
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1. Overview of 43 Years of Studies on Asymmetric Synthesis;YAKUGAKU ZASSHI;2020-02-01
2. Grinding assisted, column chromatography free decarboxylative carbon-carbon bond formation: Greener synthesis of 3, 3-disubstituted oxindoles;Tetrahedron;2017-02
3. A dynamic kinetic asymmetric transfer hydrogenation–cyclization tandem reaction: an easy access to chiral 3,4-dihydro-2H-pyran-carbonitriles;Chemical Communications;2017
4. Molecular sieve mediated sequential Knoevenagel condensation/decarboxylative Michael addition reaction: efficient and mild conditions for the synthesis of 3,3-disubstituted oxindoles with an all carbon quaternary center;RSC Advances;2016
5. Biocatalytic one-pot three-component synthesis of 3,3′-disubstituted oxindoles and spirooxindole pyrans using α-amylase from hog pancreas;RSC Advances;2015
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