Literature DB >> 19841813

Aminations of allylic phenyl ethers via micellar catalysis at room temperature in water.

Takashi Nishikata1, Bruce H Lipshutz.   

Abstract

Especially mild, organic solvent-free conditions have been found that allow for allylic ethers to undergo Pd-catalyzed aminations.

Entities:  

Year:  2009        PMID： 19841813      PMCID： PMC3359133          DOI： 10.1039/b914982a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  11 in total

1.  Nickel-catalyzed cross-coupling of aryl grignard reagents with aromatic alkyl ethers: an efficient synthesis of unsymmetrical biaryls.

Authors:  John W Dankwardt
Journal:  Angew Chem Int Ed Engl       Date:  2004-04-26       Impact factor: 15.336

2.  Reactions in micellar systems.

Authors:  Torsten Dwars; Eckhard Paetzold; Günther Oehme
Journal:  Angew Chem Int Ed Engl       Date:  2005-11-11       Impact factor: 15.336

3.  Organic reactions in aqueous media with a focus on carbon-carbon bond formations: a decade update.

Authors:  Chao-Jun Li
Journal:  Chem Rev       Date:  2005-08       Impact factor: 60.622

Review 4.  Reactions of C-H bonds in water.

Authors:  Clara I Herrerías; Xiaoquan Yao; Zhiping Li; Chao-Jun Li
Journal:  Chem Rev       Date:  2007-04-17       Impact factor: 60.622

5.  Allylic ethers as educts for Suzuki-Miyaura couplings in water at room temperature.

Authors:  Takashi Nishikata; Bruce H Lipshutz
Journal:  J Am Chem Soc       Date:  2009-09-02       Impact factor: 15.419

6.  Aminations of Aryl Bromides in Water at Room Temperature.

Authors:  Bruce H Lipshutz; David W Chung; Brian Rich
Journal:  Adv Synth Catal       Date:  2009-08       Impact factor: 5.837

7.  Amination of allylic alcohols in water at room temperature.

Authors:  Takashi Nishikata; Bruce H Lipshutz
Journal:  Org Lett       Date:  2009-06-04       Impact factor: 6.005

8.  Facile and selective deallylation of allyl ethers using diphosphinidenecyclobutene-coordinated palladium catalysts.

Authors:  Hiromi Murakami; Tatsuya Minami; Fumiyuki Ozawa
Journal:  J Org Chem       Date:  2004-06-25       Impact factor: 4.354

9.  Metal-catalyzed enantioselective allylation in asymmetric synthesis.

Authors:  Zhan Lu; Shengming Ma
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

10.  Nickel-catalyzed cross-coupling of aryl methyl ethers with aryl boronic esters.

Authors:  Mamoru Tobisu; Toshiaki Shimasaki; Naoto Chatani
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336
View more
  5 in total

1.  "Designer"-Surfactant-Enabled Cross-Couplings in Water at Room Temperature.

Authors:  Bruce H Lipshutz; Subir Ghorai
Journal:  Aldrichimica Acta       Date:  2012-01-01       Impact factor: 3.667

2.  Manipulating micellar environments for enhancing transition metal-catalyzed cross-couplings in water at room temperature.

Authors:  Bruce H Lipshutz; Subir Ghorai; Wendy Wen Yi Leong; Benjamin R Taft; Daniel V Krogstad
Journal:  J Org Chem       Date:  2011-05-19       Impact factor: 4.354

3.  TPGS-750-M: a second-generation amphiphile for metal-catalyzed cross-couplings in water at room temperature.

Authors:  Bruce H Lipshutz; Subir Ghorai; Alexander R Abela; Ralph Moser; Takashi Nishikata; Christophe Duplais; Arkady Krasovskiy; Ricky D Gaston; Robert C Gadwood
Journal:  J Org Chem       Date:  2011-05-09       Impact factor: 4.354

4.  Equilibrium Study of Pd(dba)2 and P(OPh)3 in the Pd-Catalyzed Allylation of Aniline by Allyl Alcohol.

Authors:  Supaporn Sawadjoon; Andreas Orthaber; Per J R Sjöberg; Lars Eriksson; Joseph S M Samec
Journal:  Organometallics       Date:  2013-12-31       Impact factor: 3.876

Review 5.  Nanoreactors for green catalysis.

Authors:  M Teresa De Martino; Loai K E A Abdelmohsen; Floris P J T Rutjes; Jan C M van Hest
Journal:  Beilstein J Org Chem       Date:  2018-03-29       Impact factor: 2.883
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.