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ChemInform Abstract: Solvent‐Free Asymmetric Conjugate Addition of Malonates to Enones Using a Diaminomethylenemalononitrile Organocatalyst.

Shin‐ichi Hirashima, Takaaki Sakai, Kosuke Nakashima, Nana Watanabe, Yuji Koseki, Kanako Mukai, Yohei Kanada, Norihiro Tada, Akichika Itoh, Tsuyoshi Miura

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Abstract

Abstract The optically active diamine title catalyst efficiently promotes the conjugate addition of malonates to enones to give the corresponding addition products in good yields with excellent enantioselectivities.

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What this paper is about

Abstract The optically active diamine title catalyst efficiently promotes the conjugate addition of malonates to enones to give the corresponding addition products in good yields with excellent enantioselectivities.

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Available abstract

Abstract The optically active diamine title catalyst efficiently promotes the conjugate addition of malonates to enones to give the corresponding addition products in good yields with excellent enantioselectivities.

Key concepts: Chemistry, Conjugate, Optically active, Catalysis, Combinatorial chemistry, Diamine, Solvent, Organocatalysis

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ChemInform Abstract: Solvent‐Free Asymmetric Conjugate Addition of Malonates to Enones Using a Diaminomethylenemalononitrile Organocatalyst. — Research Paper | ScholarLens