Affiliation & Address |
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Laboratory for Chemistry and Life Science
Institute of Integrated Research Institute of Science Tokyo
Address:R1-28, 4259 Nagatsuta, Midori-ku, Yokohama 226-8501, Japan
Phone:+81-45-924-5229 Fax:+81-45-924-5230
E-mail:catti.l.aa@m.titech.ac.jp
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Profile |
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2011 B.S. Technical University of Munich
2013 M.S. Technical University of Munich
2013-2016 Ph.D. Technical University of Munich
2016-2017 Ph.D. & Postdoctoral researcher, University of Basel
2017-2020 JSPS Fellow & Research Assistant, Tokyo Institute of Technology
2020-2021 Project Assistant Professor, Kanazawa University (WPI-NanoLSI)
2021-2024 Assistant Professor, Tokyo Institute of Technology
2024-present Assistant Professor, Institute of Science Tokyo
Awards
2014 Jurgen Manchot prize (“outstanding chemistry degree”)
2022 Best Young Investigator Award (Redox Week in Sendai 2022)
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Publication |
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L. Catti,* S. Yasugami, S. Aoyama, N. Kishida, M. Yoshizawa*
A Photolockable Polyaromatic Capsule Designed via Regiochemical Substitution
Chem. Eur. J. 2025, 31, e202403703.
M. Endo, S. Aoyama, Y. Tsuchido, L. Catti,* M. Yoshizawa*
Umbrella-shaped Amphiphiles: Internal Alkylation of an Aromatic Micelle and Its Impact on Cavity Features
Angew. Chem. Int. Ed. 2024, 63, e202404088. Tokyo Tech News
L. Catti,* S. Aoyama, M. Yoshizawa*
Facile Access to Pyridinium-Based Bent Aromatic Amphiphiles: Nonionic Surface Modification of Nanocarbons in Water
Beilstein J. Org. Chem. 2024, 20, 32-40.
S. Aoyama, L. Catti,* M. Yoshizawa*
Facile Processing of Unsubstituted π-Conjugated Aromatic Polymers through Water-solubilization Using Aromatic Micelles
Angew. Chem. Int. Ed. 2023, 62, e202306399. Tokyo Tech News
M. Yoshizawa,* L. Catti
Aromatic Micelles: toward a Third-Generation of Micelles
Proc. Jpn. Acad., Ser. B 2023, 99, 29-38.
M. Ueda, N. Kishida, L. Catti, M. Yoshizawa*
Caged Bulky Organic Dyes in a Polyaromatic Framework and Their Spectroscopic Peculiarities
Chem. Sci. 2022, 13, 8642-8648.
L. Catti,* R. Sumida, M. Yoshizawa*
Aqueous Polyaromatic Receptors for Biomolecules with High Selectivity
Coord. Chem. Rev. 2022, 460, 214460.
L. Catti, H. Narita, Y. Tanaka, H. Sakai, T. Hasobe, N. V. Tkachenko, M. Yoshizawa
Supramolecular Singlet Fission of Pentacene Dimers within Polyaromatic Capsules
J. Am. Chem. Soc. 2021, 143, 9361-9367.
H. Narita, L. Catti, M. Yoshizawa
An Aromatic Micelle-based Saccharide Cluster with Changeable Fluorescent Color and its Protein Interactions
Angew. Chem. Int. Ed. 2021, 60, 12791-12795.
T. Tsutsui, L. Catti, K. Yoza, M. Yoshizawa
An Atropisomeric M2L4 Cage Mixture Displaying Guest-Induced Convergence and Strong Guest Emission in Water
Chem. Sci. 2020, 11, 8145-8150.
H. Dobashi, L. Catti, Y. Tanaka, M. Akita, M. Yoshizawa
N-Doping of Polyaromatic Capsules: Small Cavity Modification Leads to Large Change in Host-Guest Interactions
Angew. Chem. Int. Ed. 2020, 59, 11881-11885.
M. Yoshizawa, L. Catti Bent Anthracene Dimers as Versatile Building Blocks for Supramolecular Capsules
Acc. Chem. Res., 2019, 52, 2392-2404.
Y. Satoh, L. Catti, M. Akita, M. Yoshizawa A Redox-Active Heterocyclic Capsule: Radical Generation, Oxygenation, and Guest Uptake/Release
J. Am. Chem. Soc., 2019, 141, 12268-12273.
L. Catti, N. Kishida, T. Kai, M. Akita, M. Yoshizawa
Polyaromatic Nanocapsules as Photoresponsive Hosts in Water
Nature Commun., 2019, 10, 1948.
K. Yazaki, L. Catti, M. Yoshizawa
Polyaromatic Molecular Tubes: from Strategic Synthesis to Host Functions
Chem. Commun., 2018, 54, 3195-3206 (feature article).
=== K. Tiefenbacher Group ========
F. Huck, L. Catti, G. L. Reber, K. Tiefenbacher*
Expanding the Protecting Group Scope for the Carbonyl Olefin Metathesis Approach to 2,5-Dihydropyrroles
J. Org. Chem. 2022, 87, 419-428.
S. Merget, L. Catti, S. Zev, D. T. Major, N. Trapp, K. Tiefenbacher
Concentration-Dependent Self-Assembly of an Unusually Large Hexameric Hydrogen-Bonded Molecular Cage
Chem. Eur. J. 2021, 27, 4447.
S. Merget, L. Catti, G. M. Piccini, K. Tiefenbacher
Requirements for Terpene Cyclizations inside the Supramolecular Resorcinarene Capsule: Bound Water and Its Protonation Determine the Catalytic Activity
J. Am. Chem. Soc. 2020, 142, 4400.
Q. Zhang, L. Catti, L.-D. Syntrivanis, K. Tiefenbacher
En route to terpene natural products utilizing supramolecular cyclase mimetics
Nat. Prod. Rep., 2019, 36 1619.
Q. Zhang, L. Catti, K. Tiefenbacher
Catalysis inside the Hexameric Resorcinarene Capsule
Acc. Chem. Res., 2018, 51, 2107-2114.
L. Catti, K. Tiefenbacher
Brosted Acid-Catalyzed Carbonyl-Olefin Metathesis inside a Self-Assembled Supramolecular Host
Angew. Chem. Int. Ed. 2018, 57, 14589-14592.
Q. Zhang, L. Catti, J. Pleiss, K. Tiefenbacher
Terpene Cyclizations inside a Supramolecular Catalyst: Leaving-Group-Controlled Product Selectivity and Mechanistic Studies
J. Am. Chem. Soc. 2017, 139, 11482-11492.
L. Catti, A. Pothig, K. Tiefenbacher
Host-Catalyzed Cyclodehydration-Rearrangement Cascade Reaction of Unsaturated Tertiary Alcohols
Adv. Synth. Catal. 2017, 359, 1331-1338.
Q. Zhang, L. Catti, V. R. I. Kaila, K. Tiefenbacher
To catalyze or not to catalyze: elucidation of the subtle differences between the hexameric capsules of pyrogallolarene and resorcinarene
Chem. Sci. 2017, 8, 1653-1657.
L. Catti, T. Brauer, Q. Zhang, K. Tiefenbacher
Exploring Catalysis inside Self-Assembled Supramolecular Containers
Chimia 2016, 70, 810-814.
L. Catti, Q. Zhang, K. Tiefenbacher
Advantages of Catalysis in Self-Assembled Molecular Capsules
Chem. Eur. J. 2016, 22, 9060-9066.
L. Catti, Q. Zhang, K. Tiefenbacher
Self-Assembled Supramolecular Structures as Catalysts for Reactions Involving Cationic Transition States
Synthesis 2016, 48, 313-328. (selected as cover article)
L. Catti, K. Tiefenbacher
Intramolecular hydroalkoxylation catalyzed inside a self-assembled cavity of an enzyme-like host structure
Chem. Commun. 2015, 51, 892-894.
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