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- Enzymatically triggered chromogenic cross-linking agents under physiological conditions. Hikaru Fujita, Jinghuai Dou, Nobuyuki Matsumoto, Zhiyuan Wu, Jonathan S. Lindsey
, New J. Chem.
, 2020
, 44
, 719
- Silacyclization through palladium-catalyzed intermolecular silicon-based C(sp2)–C(sp3) cross-coupling. Ying Qin, Lianghui Li, Jin-Yuan Liang, Kailong Li, Dongbing Zhao
, Chem. Sci.
, 2021
, 12
, 14224
- Frustrated Lewis pair olefin addition reactions: P-, N-, C- and H-based nucleophilic additions to an olefin-tethered borane. Xiaoxi Zhao, Douglas W. Stephan
, Chem. Sci.
, 2012
, 3
, 2123
- Chromogenic agents built around a multifunctional double-triazine framework for enzymatically triggered cross-linking under physiological conditions. Hikaru Fujita, Yunlong Zhang, Zhiyuan Wu, Jonathan S. Lindsey
, New J. Chem.
, 2020
, 44
, 3856
- Differences in Al distribution and acidic properties between RTH-type zeolites synthesized with OSDAs and without OSDAs. Ming Liu, Toshiyuki Yokoi, Masato Yoshioka, Hiroyuki Imai, Junko N. Kondo, Takashi Tatsumi
, Phys. Chem. Chem. Phys.
, 2014
, 16
, 4155
- Reversible, metal-free hydrogen
activation by frustrated Lewis pairs. Chunfang Jiang, Olivier Blacque, Thomas Fox, Heinz Berke
, Dalton Trans.
, 2011
, 40
, 1091
- Organoboron-based multiple-resonance emitters: synthesis, structure–property correlations, and prospects. Masashi Mamada, Masahiro Hayakawa, Junki Ochi, Takuji Hatakeyama
, Chem. Soc. Rev.
, 2024
, 53
, 1624
- Nitroxide radical-containing polynorbornenes by ring-opening metathesis polymerization as stabilizing agents for polyolefins. Clémence Nicolas, Laurent Fontaine, Véronique Montembault
, Polym. Chem.
, 2019
, 10
, 5487
- Recent advances in enantioselective organocatalyzed anhydride desymmetrization and its application to the synthesis of valuable enantiopure compounds. María D. Díaz de Villegas, José A. Gálvez, Pablo Etayo, Ramón Badorrey, Pilar López-Ram-de-Víu
, Chem. Soc. Rev.
, 2011
, 40
, 5564
- Cobaltate anion couples terminal dienes with trifluoroacetic anhydride: a direct fluoroacylation of 1,3-dienes. Benjamin L. Kohn, Tomislav Rovis
, Chem. Sci.
, 2014
, 5
, 2889