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Side-Arm-Promoted Highly Enantioselective Ring-Opening Reactions and Kinetic Resolution of Donor–Acceptor Cyclopropanes with Amines

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Figshare2016-02-20 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Side_Arm_Promoted_Highly_Enantioselective_Ring_Opening_Reactions_and_Kinetic_Resolution_of_Donor_Acceptor_Cyclopropanes_with_Amines/2516413
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A Ni-catalyzed asymmetric ring-opening reaction of 2-substituted cyclopropane-1,1-dicarboxylates with aliphatic amines has been accomplished using the chiral indane–trisoxazoline (In-TOX) ligand. This highly enantioselective reaction provides an efficient approach to a variety of chiral γ-substituted γ-amino acid derivatives, which are readily transformed into multifunctionalized piperidines and γ-lactams. The single-crystal X-ray structure of the TOX–Ni complex is provided, and the role of the side arm in the chiral ligand is discussed.
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2016-02-20
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