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    <subfield code="a">Cored, Jorge</subfield>
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    <subfield code="a">Enantioselective Friedel-Crafts alkylation of 1,3,5-trimethoxybenzene with trans-ß-nitrostyrenes catalysed by [Cp*Rh{(R)-Prophos}(H2O)][SbF6]2 (Prophos = propane-1,2-diyl-bis(diphenylphosphane)</subfield>
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    <subfield code="a">The aqua complex (SRh,RC)-[Cp*Rh{(R)-Prophos}(H2O)][SbF6]2 (Prophos = propane-1,2-diyl-bis(diphenylphosphane) catalyses the asymmetric Friedel-Crafts (FC) alkylation of 1,3,5-trimethoxybenzene with trans-β-nitrostyrenes. Only the monoalkylated adduct was obtained in all cases with enantioselectivities of up to 93/7 e.r. Solution NMR measurements have allowed us to detect and characterise catalytic intermediates such as metal-trans-β-nitrostyrene and metal‑aci-nitro complexes, as well as free aci‑nitro compound. Based on these studies, a Michael-type Friedel-Crafts mechanism is proposed.</subfield>
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    <subfield code="a">Sánchez, Antonio</subfield>
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    <subfield code="1">2010</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Química Inorgánica</subfield>
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    <subfield code="g">1021 (2024), 123377 [13 pp.]</subfield>
    <subfield code="p">J. organomet. chem.</subfield>
    <subfield code="t">Journal of Organometallic Chemistry</subfield>
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