Synlett
DOI: 10.1055/a-2648-9222
letter

Regiodivergent Asymmetric Conjugate Addition of 2-Furfuryl Ketones to Nitroalkenes Using Thiourea Organocatalysts

Taro Koda
1   Faculty of Pharmacy and Pharmaceutical Sciences, Josai University, Sakado, Japan
,
1   Faculty of Pharmacy and Pharmaceutical Sciences, Josai University, Sakado, Japan
,
Mitsuaki Suzuki
2   Faculty of Sciences, Josai University, Sakado, Japan
,
Kosuke Nakashima
3   School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan
,
Shin-ichi Hirashima
3   School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan
,
Akihiro Yoshida
1   Faculty of Pharmacy and Pharmaceutical Sciences, Josai University, Sakado, Japan
,
Tsuyoshi Miura
3   School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan
,
Takashi Yamanoi
1   Faculty of Pharmacy and Pharmaceutical Sciences, Josai University, Sakado, Japan
› Institutsangaben


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Abstract

We recently reported the asymmetric ε-regioselective conjugate addition of 2-furfuryl ketones to nitroalkenes utilizing a thiourea–pyrrolidine organocatalyst, resulting in good yields and enantioselectivities. In this study, we present a novel approach for the asymmetric α-regioselective conjugate addition of 2-furfuryl ketones to nitroalkenes using a thiourea–tertiary amine organocatalyst, which has not been previously documented. The reactions produced α-regioselective addition products in high yields and with excellent stereoselectivities. Thus, this work marks the first example of regiodivergent asymmetric conjugate addition of 2-furfuryl ketones to nitroalkenes.

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Publikationsverlauf

Eingereicht: 02. Juni 2025

Angenommen nach Revision: 03. Juli 2025

Accepted Manuscript online:
03. Juli 2025

Artikel online veröffentlicht:
30. Juli 2025

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