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Items: 5

1.

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.

Chem Commun (Camb). 2012 Nov 25;48(91):11211-3. doi: 10.1039/c2cc36197c. Epub 2012 Oct 11.

PMID:
23059706
2.

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.

Chemistry. 2012 Sep 17;18(38):11871-5. doi: 10.1002/chem.201201579. Epub 2012 Aug 17.

PMID:
22903340
3.

Cross-coupling of aryllithiums with aryl and vinyl halides in flow microreactors.

Nagaki A, Moriwaki Y, Haraki S, Kenmoku A, Takabayashi N, Hayashi A, Yoshida J.

Chem Asian J. 2012 May;7(5):1061-8. doi: 10.1002/asia.201101019. Epub 2012 Feb 29.

PMID:
22378563
4.

Cross-coupling in a flow microreactor: space integration of lithiation and Murahashi coupling.

Nagaki A, Kenmoku A, Moriwaki Y, Hayashi A, Yoshida J.

Angew Chem Int Ed Engl. 2010 Oct 4;49(41):7543-7. doi: 10.1002/anie.201002763. No abstract available.

PMID:
20818635
5.

A flow microreactor system enables organolithium reactions without protecting alkoxycarbonyl groups.

Nagaki A, Kim H, Moriwaki Y, Matsuo C, Yoshida J.

Chemistry. 2010 Sep 24;16(36):11167-77. doi: 10.1002/chem.201000876.

PMID:
20715202

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