Iron-catalyzed regio- and stereoselective carbolithiation of Alkynes

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Abstract

Butylation problems ironed out: 3-Pentynyl ethers react with butyllithium at - 20°C in toluene, upon addition of a catalytic amount of a cheap iron(III) salt, to afford (E)-4-methyl-3-octenyl ethers in high yields. Stereochmically defined tetrasubstituted alkenes were also obtained by the subsequent addition of electrophiles (E+, see scheme; acac = acetylacetonate, Bn = benzyl).

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Hojo, M., Murakami, Y., Aihara, H., Sakuragi, R., Baba, Y., & Hosomi, A. (2001). Iron-catalyzed regio- and stereoselective carbolithiation of Alkynes. Angewandte Chemie - International Edition, 40(3), 621–623. https://doi.org/10.1002/1521-3773(20010202)40:3<621::AID-ANIE621>3.0.CO;2-O

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