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2010 | 2 |
2012 | 3 |
2024 | 0 |
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Page 1
Cross-coupling of aryllithiums with aryl and vinyl halides in flow microreactors.
Chem Asian J. 2012 May;7(5):1061-8. doi: 10.1002/asia.201101019. Epub 2012 Feb 29.
Chem Asian J. 2012.
PMID: 22378563
A flow microreactor system enables organolithium reactions without protecting alkoxycarbonyl groups.
Nagaki A, Kim H, Moriwaki Y, Matsuo C, Yoshida J.
Nagaki A, et al. Among authors: moriwaki y.
Chemistry. 2010 Sep 24;16(36):11167-77. doi: 10.1002/chem.201000876.
Chemistry. 2010.
PMID: 20715202
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Flash generation of a highly reactive Pd catalyst for Suzuki-Miyaura coupling by using a flow microreactor.
Nagaki A, Takabayashi N, Moriwaki Y, Yoshida J.
Nagaki A, et al. Among authors: moriwaki y.
Chemistry. 2012 Sep 17;18(38):11871-5. doi: 10.1002/chem.201201579. Epub 2012 Aug 17.
Chemistry. 2012.
PMID: 22903340
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Cross-coupling in a flow microreactor: space integration of lithiation and Murahashi coupling.
Nagaki A, Kenmoku A, Moriwaki Y, Hayashi A, Yoshida J.
Nagaki A, et al. Among authors: moriwaki y.
Angew Chem Int Ed Engl. 2010 Oct 4;49(41):7543-7. doi: 10.1002/anie.201002763.
Angew Chem Int Ed Engl. 2010.
PMID: 20818635
No abstract available.
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Flow synthesis of arylboronic esters bearing electrophilic functional groups and space integration with Suzuki-Miyaura coupling without intentionally added base.
Nagaki A, Moriwaki Y, Yoshida J.
Nagaki A, et al. Among authors: moriwaki y.
Chem Commun (Camb). 2012 Nov 25;48(91):11211-3. doi: 10.1039/c2cc36197c. Epub 2012 Oct 11.
Chem Commun (Camb). 2012.
PMID: 23059706
Free article.
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