| Abstract
| - Intramolecular radical cyclizations of Co2(CO)6-complexed bis-propargyl alcohols 1−5 provide an easy, two-step access to the otherwise hardly accessible d,l- and meso-3,4-diaryl-1,5-cyclodecadiynes 21−25. The acid-induced generation of bis-cations 6−10 is followed by reduction with a 100-fold excess of zinc, generating key reactive intermediates, i.e. the cobalt-complexed bis-propargyl radicals 11−15. The substitution pattern (0-, 4-, 3,4-, 3,4,5-) and the nature of aromatic substituents (H, i-Pr, OMe) are found essential both to the diastereoselectivity of the processwith d,l:meso ratios varying from 54:46 to 80:20and the isolability of individual stereoisomers. In particular, an accumulation of methoxy groups on the periphery of the aromatic rings facilitates separation in both intra- and intermolecular reactions. The observed disparity in the level of diastereoselection in intra- and intermolecular reactions is accounted for on the basis of conformational analysis, calculation data for cobalt-complexed propargyl radicals, and the concept of a CH/π coordination. The new knowledge thus acquired has a predicting power, allowing future substrates to be designed, both topologically and stereoelectronically, in a manner favoring either d,l or meso diastereomers.
- Intramolecular radical cyclizations of Co2(CO)6-complexed bis-propargyl alcohols provide an easy, two-step access to otherwise hardly accessible d,l- and meso-3,4-diaryl-1,5-cyclodecadiynes. The substitution pattern around the aromatic nuclei, CH/π coordination, and steric repulsion between para substituents have been identified as the main determinants governing the diastereoselectivity of the process.
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