Memory of chirality in reactions involving monoradicals Article Swipe
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Christian Simon Gloor
,
F. Dénès
,
Philippe Renaud
·
YOU?
·
· 2016
· Open Access
·
· DOI: https://doi.org/10.1080/10715762.2016.1232485
· OA: W2507547028
YOU?
·
· 2016
· Open Access
·
· DOI: https://doi.org/10.1080/10715762.2016.1232485
· OA: W2507547028
The effects of memory of chirality (MoC) in reactions involving monoradical species are reviewed here. Reactions involving a nonracemic chiral starting material bearing a single stereogenic element such as a chiral center or chiral axis directly involved in the new bond formation are discussed. These reactions lead to a nonracemic product via an intermediate susceptible to rapid racemization. Memory of chirality has been observed in cyclic radicals, aryl, ester/amide substituted acyclic radicals, and benzylic radicals at temperatures up to 130 °C.
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