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Piles of Books

Publications

12.  The contribution of cyclic imide stereoisomers on cereblon-dependent activity

Amako, Y.†, Ichikawa, S.​†, Lloyd, H. C., Payne, N. C., Lin, Z., Boghossian, A. S., Rees, M. G., Ronan, M. M., Roth, J. A., Zhu, Q., Budnik, B., Mazitschek, R., Woo, C. M.

Chemical Science 2025Advance Article. (†equal contribution)​​

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11.  Protocol for the comprehensive biochemical and cellular profiling of small-molecule degraders using CoraFluor TR-FRET technology

Payne, N. C.†, Ichikawa, S.​†, Woo, C. M., Mazitschek, R.

STAR Protocols 20245, 103129. (†equal contribution)​​​​​​​

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​​​​​​​10.  The Cyclimids: Degron-inspired cereblon binders for targeted protein degradation

Ichikawa, S.​†, Payne, N. C.†, Xu, W., Chang, C.-F., Vallavoju, N., Frome, S., Flaxman, H. A., Mazitschek, R., Woo, C. M. 

Cell Chemical Biology 2024, 31, 1162–1175. (†equal contribution)

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9.  The E3 ligase adapter cereblon targets the C-terminal cyclic imide degron

Ichikawa, S.†, Flaxman, H. A.†, Xu, W.†, Vallavoju, N., Lloyd, H. C., Wang, B., Shen, D., Pratt, M. R., Woo, C. M.

Nature 2022610, 775–782. (†equal contribution)

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​​8.   Asymmetric Synthesis of γ-Amino Alcohols by Copper-Catalyzed Hydroamination

Ichikawa, S., Buchwald, S. L.

Organic Letters 2019, 21, 8736–8739. 

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7.   Regio- and Enantioselective Synthesis of 1,2-Diamine Derivatives by Copper-Catalyzed Hydroamination

Ichikawa, S., Dai, X.-J., Buchwald, S. L.

Organic Letters 2019, 21, 4370–4373. 

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​6.   A Modified System for the Synthesis of Enantioenriched N-Arylamines through Copper-Catalyzed Hydroamination

Ichikawa, S., Zhu, S., Buchwald, S. L.

Angewandte Chemie International Edition 2018, 57, 8714–8718.

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5.   Rapid and Efficient Copper-Catalyzed Finkelstein Reaction of (Hetero)Aromatics under Continuous-Flow Conditions

Chen, M., Ichikawa, S., Buchwald, S. L.

Angewandte Chemie International Edition 2015, 54, 263–266.

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4.   Iron-Catalyzed Directed Alkylation of Alkenes and Arenes with Alkylzinc Halides

Ilies, L., Ichikawa, S., Asako, S., Matsubara, T., Nakamura, E.

Advanced Synthesis & Catalysis 2015, 357, 2175–2179.

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3.  Iron-Catalyzed Directed Alkylation of Aromatic and Olefinic Carboxamides with Primary and Secondary Alkyl Tosylates, Mesylates, and Halides

Ilies, L., Matsubara, T., Ichikawa, S., Asako, S., Nakamura, E.

Journal of the American Chemical Society 2014, 136, 13126–13129.

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2.   Theoretical Study on Alkoxydiphosphine Ligand for Bimetallic Cooperation in Nickel-Catalyzed Monosubstitution of C–F Bond

Asako, S., Ilies, L., Verma, P., Ichikawa, S., Nakamura, E.

Chemistry Letters 2014, 43, 726–728.

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1.   Fluorescent azadipyrrinato zinc(II) complex: hybridisation with a dipyrrinato ligand

Sakamoto, R., Kusaka, S., Kitagawa, Y., Kishida, M., Hayashi, M., Takara, Y., Tsuchiya, M., Kakinuma, J., Takeda, T., Hirata, K., Ogino, T., Kawahara, K., Yagi, T., Ikehira, S., Nakamura, T., Isomura, M., Toyama, M., Ichikawa, S., Okumura, M., Nishihara, H.

Dalton Transactions 2012, 41, 14035–14037.

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ICHIKAWA LAB

Department of Molecular Medicine @ Cornell University

C3-172/174 VMC, 930 Campus Road, Ithaca, NY 14853

©2024 by Ichikawa Lab.

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