Literature DB >> 24447127

"Nok": a phytosterol-based amphiphile enabling transition-metal-catalyzed couplings in water at room temperature.

Piyatida Klumphu1, Bruce H Lipshutz.   

Abstract

The third-generation designer amphiphile/surfactant, "Nok" (i.e., SPGS-550-M; β-sitosterol methoxypolyethyleneglycol succinate), soon to be commercially available from Aldrich, can be prepared in two steps using an abundant plant feedstock and β-sitosterol, together with succinic anhydride and PEG-550-M. Upon dissolution in water, it forms nanomicelles that serve as nanoreactors, which can be characterized by both cryo-TEM and dynamic light scattering analyses. Several transition-metal-catalyzed reactions have been run under micellar conditions to evaluate this surfactant relative to results obtained in nanoparticles composed of TPGS-750-M (i.e., a second-generation surfactant). It is shown that Nok usually affords yields that are, in general, as good or better than those typically obtained with TPGS-750-M, and yet is far less costly.

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Year:  2014        PMID: 24447127      PMCID: PMC4013797          DOI: 10.1021/jo401744b

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  36 in total

1.  Ruthenium-catalyzed C-H/N-O bond functionalization: green isoquinolone syntheses in water.

Authors:  Lutz Ackermann; Sabine Fenner
Journal:  Org Lett       Date:  2011-11-11       Impact factor: 6.005

2.  A novel polymer-supported arene-ruthenium complex for ring-closing olefin metathesis.

Authors:  Ryo Akiyama; Shū Kobayashi
Journal:  Angew Chem Int Ed Engl       Date:  2002-07-15       Impact factor: 15.336

3.  Palladium-catalyzed amidation of aryl halides using 2-dialkylphosphino-2'-alkoxyl-1,1'-binaphthyl as ligands.

Authors:  Fangfang Ma; Xiaomin Xie; Lei Zhang; Zhiyong Peng; Lina Ding; Lei Fu; Zhaoguo Zhang
Journal:  J Org Chem       Date:  2012-05-31       Impact factor: 4.354

4.  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

5.  Organic chemistry in water.

Authors:  Chao-Jun Li; Liang Chen
Journal:  Chem Soc Rev       Date:  2005-11-21       Impact factor: 54.564

6.  Miyaura Borylations of Aryl Bromides in Water at Room Temperature.

Authors:  Bruce H Lipshutz; Ralph Moser; Karl R Voigtritter
Journal:  Isr J Chem       Date:  2010-12-01       Impact factor: 3.333

7.  Pd(PhCN)(2)Cl(2)/P(t-Bu)(3): a versatile catalyst for Sonogashira reactions of aryl bromides at room temperature.

Authors:  T Hundertmark; A F Littke; S L Buchwald; G C Fu
Journal:  Org Lett       Date:  2000-06-15       Impact factor: 6.005

Review 8.  Phytosterols, phytostanols, and their conjugates in foods: structural diversity, quantitative analysis, and health-promoting uses.

Authors:  Robert A Moreau; Bruce D Whitaker; Kevin B Hicks
Journal:  Prog Lipid Res       Date:  2002-11       Impact factor: 16.195

Review 9.  Potential uses and benefits of phytosterols in diet: present situation and future directions.

Authors:  J QuIlez; P GarcIa-Lorda; J Salas-Salvadó
Journal:  Clin Nutr       Date:  2003-08       Impact factor: 7.324

10.  One-pot synthesis of diarylamines from two aromatic amines via oxidative dearomatization-imino exchange-reductive aromatization.

Authors:  Li Zhang; Weibin Wang; Renhua Fan
Journal:  Org Lett       Date:  2013-04-08       Impact factor: 6.005

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  11 in total

1.  Reductions of aryl bromides in water at room temperature.

Authors:  James C Fennewald; Evan B Landstrom; Bruce H Lipshutz
Journal:  Tetrahedron Lett       Date:  2015-06-03       Impact factor: 2.415

2.  HandaPhos: A General Ligand Enabling Sustainable ppm Levels of Palladium-Catalyzed Cross-Couplings in Water at Room Temperature.

Authors:  Sachin Handa; Martin P Andersson; Fabrice Gallou; John Reilly; Bruce H Lipshutz
Journal:  Angew Chem Int Ed Engl       Date:  2016-02-29       Impact factor: 15.336

Review 3.  Energy-Saving Pathways for Thermoelectric Nanomaterial Synthesis: Hydrothermal/Solvothermal, Microwave-Assisted, Solution-Based, and Powder Processing.

Authors:  Nagaraj Nandihalli; Duncan H Gregory; Takao Mori
Journal:  Adv Sci (Weinh)       Date:  2022-07-17       Impact factor: 17.521

Review 4.  Cascade Processes with Micellar Reaction Media: Recent Advances and Future Directions.

Authors:  Christina Tang; Bridget T McInnes
Journal:  Molecules       Date:  2022-08-31       Impact factor: 4.927

Review 5.  Replacement of Less-Preferred Dipolar Aprotic and Ethereal Solvents in Synthetic Organic Chemistry with More Sustainable Alternatives.

Authors:  Andrew Jordan; Callum G J Hall; Lee R Thorp; Helen F Sneddon
Journal:  Chem Rev       Date:  2022-02-24       Impact factor: 72.087

6.  Transitioning organic synthesis from organic solvents to water. What's your E Factor?

Authors:  Bruce H Lipshutz; Subir Ghorai
Journal:  Green Chem       Date:  2014-08-01       Impact factor: 10.182

7.  Designer Micelles Accelerate Flux Through Engineered Metabolism in E. coli and Support Biocompatible Chemistry.

Authors:  Stephen Wallace; Emily P Balskus
Journal:  Angew Chem Int Ed Engl       Date:  2016-04-08       Impact factor: 15.336

8.  Kumada-Grignard-type biaryl couplings on water.

Authors:  Anish Bhattacharjya; Piyatida Klumphu; Bruce H Lipshutz
Journal:  Nat Commun       Date:  2015-06-18       Impact factor: 14.919

Review 9.  Multicomponent Reactions Accelerated by Aqueous Micelles.

Authors:  Daniel Paprocki; Arleta Madej; Dominik Koszelewski; Anna Brodzka; Ryszard Ostaszewski
Journal:  Front Chem       Date:  2018-10-22       Impact factor: 5.221

10.  Micellar catalysis-enabled sustainable ppm Au-catalyzed reactions in water at room temperature.

Authors:  Piyatida Klumphu; Camille Desfeux; Yitao Zhang; Sachin Handa; Fabrice Gallou; Bruce H Lipshutz
Journal:  Chem Sci       Date:  2017-07-20       Impact factor: 9.825

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