Fluorous Catalysis

László T. Mika, I. Horváth

Research output: Chapter in Book/Report/Conference proceeding › Chapter

5 Citations (Scopus)
Original languageEnglish
Title of host publicationGreen Techniques for Organic Synthesis and Medicinal Chemistry
PublisherJohn Wiley and Sons
Pages137-184
Number of pages48
ISBN (Print)9780470711514
DOIs
Publication statusPublished - May 29 2012

Fingerprint

Catalysis

Keywords

  • Asymmetric hydrogenation, using prochiral substrates
  • Catalytic hydrosilylation, chemical transformation for silicon compounds
  • Fluorous biphase reaction
  • Fluorous catalysis
  • Fluorous organocatalysis, Hajos-Parrish-Eder-Sauer-Wiechert reaction
  • Fluorous transition metal catalysts and ligands
  • Negishi coupling of arylzinc bromides, and fluorous Suzuki coupling
  • Phosphine-free palladium-catalyzed Heck reaction
  • Product/catalyst separation and SFLP catalysis
  • Temperature-dependent fluorous-solid/liquid biphase concept

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Pharmacology, Toxicology and Pharmaceutics(all)

Cite this

Mika, L. T., & Horváth, I. (2012). Fluorous Catalysis. In Green Techniques for Organic Synthesis and Medicinal Chemistry (pp. 137-184). John Wiley and Sons. https://doi.org/10.1002/9780470711828.ch6

Fluorous Catalysis. / Mika, László T.; Horváth, I.

Green Techniques for Organic Synthesis and Medicinal Chemistry. John Wiley and Sons, 2012. p. 137-184.

Research output: Chapter in Book/Report/Conference proceeding › Chapter

Mika, LT & Horváth, I 2012, Fluorous Catalysis. in Green Techniques for Organic Synthesis and Medicinal Chemistry. John Wiley and Sons, pp. 137-184. https://doi.org/10.1002/9780470711828.ch6
Mika LT, Horváth I. Fluorous Catalysis. In Green Techniques for Organic Synthesis and Medicinal Chemistry. John Wiley and Sons. 2012. p. 137-184 https://doi.org/10.1002/9780470711828.ch6
Mika, László T. ; Horváth, I. / Fluorous Catalysis. Green Techniques for Organic Synthesis and Medicinal Chemistry. John Wiley and Sons, 2012. pp. 137-184
@inbook{3cd28e49c6bb42be9f31ffb4703b50ff,
title = "Fluorous Catalysis",
keywords = "Asymmetric hydrogenation, using prochiral substrates, Catalytic hydrosilylation, chemical transformation for silicon compounds, Fluorous biphase reaction, Fluorous catalysis, Fluorous organocatalysis, Hajos-Parrish-Eder-Sauer-Wiechert reaction, Fluorous transition metal catalysts and ligands, Negishi coupling of arylzinc bromides, and fluorous Suzuki coupling, Phosphine-free palladium-catalyzed Heck reaction, Product/catalyst separation and SFLP catalysis, Temperature-dependent fluorous-solid/liquid biphase concept",
author = "Mika, {L{\'a}szl{\'o} T.} and I. Horv{\'a}th",
year = "2012",
month = "5",
day = "29",
doi = "10.1002/9780470711828.ch6",
language = "English",
isbn = "9780470711514",
pages = "137--184",
booktitle = "Green Techniques for Organic Synthesis and Medicinal Chemistry",
publisher = "John Wiley and Sons",

}

TY - CHAP

T1 - Fluorous Catalysis

AU - Mika, László T.

AU - Horváth, I.

PY - 2012/5/29

Y1 - 2012/5/29

KW - Asymmetric hydrogenation, using prochiral substrates

KW - Catalytic hydrosilylation, chemical transformation for silicon compounds

KW - Fluorous biphase reaction

KW - Fluorous catalysis

KW - Fluorous organocatalysis, Hajos-Parrish-Eder-Sauer-Wiechert reaction

KW - Fluorous transition metal catalysts and ligands

KW - Negishi coupling of arylzinc bromides, and fluorous Suzuki coupling

KW - Phosphine-free palladium-catalyzed Heck reaction

KW - Product/catalyst separation and SFLP catalysis

KW - Temperature-dependent fluorous-solid/liquid biphase concept

UR - http://www.scopus.com/inward/record.url?scp=84886152916&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84886152916&partnerID=8YFLogxK

U2 - 10.1002/9780470711828.ch6

DO - 10.1002/9780470711828.ch6

M3 - Chapter

SN - 9780470711514

SP - 137

EP - 184

BT - Green Techniques for Organic Synthesis and Medicinal Chemistry

PB - John Wiley and Sons

ER -

Access to Document