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Enantioselective Protonation of Radical Anion Intermediates in Photoallylation and Photoreduction Reactions of 3,3-Diaryl-1,1-dicyano-2-methylprop-1-ene with Allyltrimethylsilane.

ABSTRACT: Photoreactions of acetonitrile solutions of 3,3-diaryl-1,1-dicyano-2-methylprop-1-enes (1a-c) with allyltrimethylsilane (2) in the presence of phenanthrene as a photoredox catalyst and acetic acid as a proton source formed photoallylation (3) and photoreduction (4) products via photoinduced electron transfer pathways. When (S)-mandelic acid was used as the proton source, the reactions proceeded with 3.4 and 4.8 %ee for formation of 3 and 4, respectively. The results of studies of the effect of aryl ring substituents and several chiral carboxylic acids suggested that the enantioselectivities of the reactions are governed by steric controlled proton transfer in intermediate complexes formed by π-π and OH-π interactions of anion radicals derived from 1a-c and chiral carboxylic acids.

SUBMITTER: Maeda H 

PROVIDER: S-EPMC6680834 | biostudies-literature | 2019 Jul

REPOSITORIES: biostudies-literature

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Enantioselective Protonation of Radical Anion Intermediates in Photoallylation and Photoreduction Reactions of 3,3-Diaryl-1,1-dicyano-2-methylprop-1-ene with Allyltrimethylsilane.

Maeda Hajime H   Iida Masayuki M   Ogawa Daisuke D   Mizuno Kazuhiko K  

Molecules (Basel, Switzerland) 20190723 14

Photoreactions of acetonitrile solutions of 3,3-diaryl-1,1-dicyano-2-methylprop-1-enes (<b>1a</b>-<b>c</b>) with allyltrimethylsilane (<b>2</b>) in the presence of phenanthrene as a photoredox catalyst and acetic acid as a proton source formed photoallylation (<b>3</b>) and photoreduction (<b>4</b>) products via photoinduced electron transfer pathways. When (<i>S</i>)-mandelic acid was used as the proton source, the reactions proceeded with 3.4 and 4.8 %ee for formation of <b>3</b> and <b>4</b>,  ...[more]

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