Photo-Organocatalytic Enantioselective Radical Cascade Reactions of Unactivated Olefins.

Photo-Organocatalytic Enantioselective Radical Cascade Reactions of Unactivated Olefins.
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DOI:
10.1002/anie.201808183
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发表时间:
2018-09-24
期刊:
Angewandte Chemie (International ed. in English)
影响因子:
--
通讯作者:
Melchiorre P
Melchiorre P
中科院分区:
其他
文献类型:
--
作者:
Bonilla P;Rey YP;Holden CM;Melchiorre P

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Radical cascade processes are invaluable for their ability to rapidly construct complex chiral molecules from simple substrates. However, implementing catalytic asymmetric variants is difficult. Reported herein is a visible‐light‐mediated organocatalytic strategy that exploits the excited‐state reactivity of chiral iminium ions to trigger radical cascade reactions with high enantioselectivity. By combining two sequential radical‐based bond‐forming events, the method converts unactivated olefins and α,β‐unsaturated aldehydes into chiral adducts in a single step. The implementation of an asymmetric three‐component radical cascade further demonstrates the complexity‐generating power of this photochemical strategy.
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