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Communication | Special issue | Vol 7, No. 1, 1977, pp.171-178
Published online, 1st January, 1970
DOI: 10.3987/S-1977-01-0171
Synthesis of 1,5-Dienes and 6-Azabicyclo[3.2.1]octanes via ω-Carbinollactams

Anthonia R. C. Oostveen, Jan J. J. de Boer, and W. Nico Speckamp*

*Laboratory of Organic Chemistry, University of Amsterdam, Nieuwe Achtergracht 129,1018 WS Amsterdam, The Netherlands


3,3-Disubstituted succinimides are reduced regioselectively at the 2 and 5 positions. The resulting ω-carbinol-lactams are used for synthesis of 6-phenyl-1,5-dienes and 6-azabicyclo[3.2.l]octanes, respectively.