13. Nickel-Catalyzed Thioesterification Enabled by a Visible-Light Organophotoredox Catalyst under Mild Conditions
Zheng, W.; Xu, Y.; Lin, L.* ChemPhotoChem 2022, 6, DOI:10.1002/cptc.202100264
12. Cobalt(III)/Chiral Carboxylic Acid-Catalyzed Enantioselective Synthesis of Benzothiadiazine-1-Oxides via C–H Activation
Hirata, Y.; Sekine, D.; Kato, Y.; Lin, L.; Kojima, M.; Yoshino, T.*; Matsunaga, S.* Angew. Chem., Int. Ed. 2022, DOI: 10.1002/anie.202205341
11. Ru(II)/Chiral Carboxylic Acid-Catalyzed Enantioselective C–H Functionalization of Sulfoximines
Huang, L.-T.; Hirata, Y.; Kato, Y.; Lin, L.; Kojima, M.; Yoshino, T.*; Matsunaga, S.* Synthesis 2021, 53, published on web. DOI: 10.1055/a-1588-0072
10. Development of Pseudo-C2-symmetric Chiral Binaphthyl Monocarboxylic Acids for Enantioselective C(sp3)–H Functionalization Reactions under Rh(III) Catalysis
Kato,Y.; Lin, L*; Kojima, M.; Yoshino, T.*; Matsunaga S.* ACS Catalysis 2021, 11, 4271−4277.
9. Photocatalytic Generation of π-allyltitanium Complexes via Radical intermediates
Li, F.; Lin,S.; Chen,Y.; Shi, C.; Yan, H.; Li, C.; Wu, C.; Lin, L.; Duan, C.; Shi, L. * Angew. Chem. Int. Ed. 2021, 60, 1561 –1566.
8. Cp2TiIIICl Catalysis in a New Light
Chen, Y.; Lin, S.; Li, F.; Zhang, X.; Lin, L.; Shi, L.* ChemPhotoChem 2020, 4, 659–663.
Before DLUT
7. Chiral Carboxylic Acid‐Enabled Achiral Rhodium(III)-Catalyzed Enantioselective C−H Functionalization
Lin, L*; Fukagawa, S.; Sekine, D.; Tomita, E.; Yoshino, T.*; Matsunaga S.* Angew. Chem. Int. Ed. 2018. 57, 12048-12052. (SYNFACT)
6. Palladium-Catalyzed Long-Range Deconjugative Isomerization of Highly Substituted α,β-Unsaturated Carbonyl Compounds
Lin, L.; Romano, C.; Mazet, C. * J. Am. Chem. Soc. 2016, 138, 10344−10350.
5. Catalytic Asymmetric Iterative/Domino Aldehyde Cross-Aldol Reactions for the Rapid and Flexible Synthesis of 1,3-Polyols.
Lin, L.; Yamamoto, K.; Mitsunuma, H.; Kanzaki, Y.; Matsunaga, S. * Kanai, M. * J. Am. Chem. Soc. 2015, 137, 15418–15421. (SYNFACT of the month)
4. Scope and mechanism in palladium-catalyzed isomerizations of highly substituted allylic, homoallylic, and alkenyl alcohols.
Larionov, E.; Lin, L.; Guénée, L.; Mazet, C.* J. Am. Chem. Soc. 2014, 136, 16882–16994.
3. Rh-catalyzed aldehyde-aldehyde cross-aldol reaction under base-free conditions: in situ aldehyde-derived enolate formation through orthogonal activation.
Lin, L.; Yamamoto, K.: Matsunaga, S. *; Kanai, M. * Chem. Asian J. 2013, 8, 2974-2983. (Selected as a Frontispiece)
2. Rhodium-catalyzed cross-aldol reaction: In situ aldehyde-enolate formation from allyloxyboranes and primary allylic alcohols
Lin, L.; Yamamoto, K.: Matsunaga, S.; Kanai, M. * Angew. Chem. Int. Ed. 2012, 51, 10275–10279. (SYNFACT)
1. Catalytic asymmetric Ring-Opening of meso-Aziridines with malonates under heterodinuclear rare earth metal schiff base catalysis
Xu, Y.; Lin,L.; Kanai, M.; Matsunaga, S. *; Shibasaki, M. * J. Am. Chem. Soc. 2011, 133, 5791–5793.
