Green Chemistry, volume 19, issue 7, pages 1647-1652

Continuous flow ring-closing metathesis, an environmentally-friendly route to 2,5-dihydro-1H-pyrrole-3-carboxylates

Marcin Drop ¹

Xavier Bantreil ²

Katarzyna Grychowska ¹

Gilbert Umuhire Mahoro ²

Evelina Colacino ²

Maciej Pawłowski ¹

Jean Martinez ^{2, 3}

Gilles Subra ³

Pawel Zajdel ¹

Frédéric Lamaty ²

Show full list: 10 authors

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Department of Medicinal Chemistry, Jagiellonian University Medical College, 9 Medyczna Street, 30-688 Krakow, Poland |

Institut des Biomolécules Max Mousseron (IBMM) UMR 5247, CNRS, Université de Montpellier, ENSCM, Université de Montpellier, Campus Triolet Place Eugène Bataillon, Montpellier cedex 5, France |

Institut des Biomolécules Max Mousseron (IBMM) UMR 5247, CNRS, Université de Montpellier, ENSCM, Bâtiment E, Faculté de Pharmacie 15, avenue Charles Flahault BP14491, Montpellier cedex 5, France |

Publication type: Journal Article

Publication date: 2017-02-16

Royal Society of Chemistry (RSC)

Journal: Green Chemistry

scimago Q1

SJR: 1.878

CiteScore: 16.1

Impact factor: 9.3

ISSN: 14639262, 14639270

DOI: 10.1039/c7gc00235a

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Environmental Chemistry

Pollution

Abstract

Ring-closing metathesis, realized in continuous flow using dimethyl carbonate as a solvent, allowed us to convert up to 10 g of dienes into important building blocks.

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Publisher

Royal Society of Chemistry (RSC)

Journal

Green Chemistry

scimago Q1

SJR

1.878

CiteScore

16.1

Impact factor

9.3

ISSN

14639262 (Print)

14639270 (Electronic)

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Continuous flow ring-closing metathesis, an environmentally-friendly route to 2,5-dihydro-1H-pyrrole-3-carboxylates

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