
Journal of Organometallic Chemistry p. 143 - 145 (1997)
Update date:2022-08-11
Topics:
Melikyan, Gagik G.
Deravakian, Asatour
A novel one-step reductive dimerization of Co-complexed propargyl alcohol 5 has been developed producing dl- and meso-(3,4-diphenyl-1,5-hexadiyne)-bis-dicobalt hexacarbonyl (8,9) with unprecedented diastereoselectivity of 90%. A tandem action of a variety of one-electron/hydride ion donors and Broensted Lewis acids has been tested both in one- and two-step methods with the latter including the isolation of propargyl cation 1.
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