Deacylative alkylation (DaA) of N-methyl-3-acetyl-2-oxindole for the synthesis of symmetrically 3,3-disubstituted 2-oxindoles. An access gate to anticancer agents and natural products.
Author:
Affiliation:
1. Universidad de Alicante, Spain; Universidad de Alicante, Spain
2. Universidad de Alicante, Spain
Publisher
FapUNIFESP (SciELO)
Subject
Multidisciplinary
Link
http://www.scielo.br/pdf/aabc/v90n1s2/0001-3765-aabc-90-01-s2-01089.pdf
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3. Enantioselective total syntheses of citrinadins A and B. Stereochemical revision of their assigned structures;BIAN Z;J Am Chem Soc,2014
4. Catalytic asymmetric synthesis of 3,3-disubstituted oxindoles: diazooxindole joins the field;CAO ZY;Tetrahedron Lett,2014
5. Enantioselective organocatalytic anti-Mannich-type reaction of N-unprotected 3-substituted 2-oxindoles with aromatic N-Ts-aldimines;CHENG L;Org Chem,2009
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