Journal
TETRAHEDRON LETTERS
Volume 48, Issue 3, Pages 461-463Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2006.11.041
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A novel and efficient two-step synthetic sequence for the preparation of 3,3-disubstituted oxindoles was developed starting from arylhydrazines and alpha-branched aldehydes via Fischer indole type synthesis followed by imine oxidation. (c) 2006 Elsevier Ltd. All rights reserved.
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