Use of Aromatic Radical-Anions in the Absence of THF. Tandem Formation and Cyclization of Benzyllithiums Derived from the Attack of Homo- and Bishomoallyllithiums on α-Methylstyrenes: Two-Pot Synthesis of Cuparene1
Author:
Affiliation:
1. Contribution from the Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja004353%2B
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1. Hydrolithiation of .alpha.-olefins by a regiospecific two-step process. Transformation of alkyl phenyl sulfides to alkyllithium reagents
2. Organoalkali compounds by radical anion induced reductive metalation of phenyl thioethers
3. Generation, some synthetic uses, and 1,2-vinyl rearrangements of secondary and tertiary homoallyllithiums, including ring contractions and a ring expansion. Remarkable acceleration of the rearrangement by an oxyanionic group
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