Green Chemistry

, том 18 , издание 18 , страницы 4947-4953

From alcohol to 1,2,3-triazole via a multi-step continuous-flow synthesis of a rufinamide precursor

Svetlana Borukhova ¹

Timothy R. Noel ^{1, 2}

Bert Metten ³

Eric De Vos ³

Volker Hessel ¹

Скрыть аффилиации авторов Показать аффилиации авторов: 3 аффилиации

Department of Chemical Engineering and Chemistry, Technische Universiteit Eindhoven, Den Dolech 2, 5600 MB Eindhoven, Netherlands |

Department of Organic Chemistry, Ghent University, Krijgslaan 281 (S4), 9000 Ghent, Belgium |

Ajinomoto OmniChem N.V., Cooppallaan 91, 9230 Wetteren, Belgium |

Тип публикации: Journal Article

Дата публикации: 2016-05-27

Royal Society of Chemistry (RSC)

Green Chemistry

scimago Q1

wos Q1

БС1

SJR: 1.928

CiteScore: 16.1

Impact factor: 9.2

ISSN: 14639262, 14639270

DOI: 10.1039/c6gc01133k

Скопировать DOI

Environmental Chemistry

Pollution

Краткое описание

Bringing the strongest suits of flow chemistry together to deliver the greenest possible process for continuous manufacturing of a rufinamide precursor.

Найдено

Топ-30

Журналы

	1 2 3 4
Journal of Flow Chemistry	Journal of Flow Chemistry, 4, 10.26% Journal of Flow Chemistry 4 публикации, 10.26%
Organic Process Research and Development	Organic Process Research and Development, 3, 7.69% Organic Process Research and Development 3 публикации, 7.69%
European Journal of Organic Chemistry	European Journal of Organic Chemistry, 2, 5.13% European Journal of Organic Chemistry 2 публикации, 5.13%
ACS Sustainable Chemistry and Engineering	ACS Sustainable Chemistry and Engineering, 2, 5.13% ACS Sustainable Chemistry and Engineering 2 публикации, 5.13%
Green Chemistry	Green Chemistry, 2, 5.13% Green Chemistry 2 публикации, 5.13%
Molecules	Molecules, 1, 2.56% Molecules 1 публикация, 2.56%
Research on Chemical Intermediates	Research on Chemical Intermediates, 1, 2.56% Research on Chemical Intermediates 1 публикация, 2.56%
International Journal of Life Cycle Assessment	International Journal of Life Cycle Assessment, 1, 2.56% International Journal of Life Cycle Assessment 1 публикация, 2.56%
iScience	iScience, 1, 2.56% iScience 1 публикация, 2.56%
Journal of Fluorine Chemistry	Journal of Fluorine Chemistry, 1, 2.56% Journal of Fluorine Chemistry 1 публикация, 2.56%
Current Opinion in Green and Sustainable Chemistry	Current Opinion in Green and Sustainable Chemistry, 1, 2.56% Current Opinion in Green and Sustainable Chemistry 1 публикация, 2.56%
Journal of Cleaner Production	Journal of Cleaner Production, 1, 2.56% Journal of Cleaner Production 1 публикация, 2.56%
Tetrahedron	Tetrahedron, 1, 2.56% Tetrahedron 1 публикация, 2.56%
Tetrahedron Letters	Tetrahedron Letters, 1, 2.56% Tetrahedron Letters 1 публикация, 2.56%
Journal of Advanced Manufacturing and Processing	Journal of Advanced Manufacturing and Processing, 1, 2.56% Journal of Advanced Manufacturing and Processing 1 публикация, 2.56%
ChemSusChem	ChemSusChem, 1, 2.56% ChemSusChem 1 публикация, 2.56%
Chemistry - A European Journal	Chemistry - A European Journal, 1, 2.56% Chemistry - A European Journal 1 публикация, 2.56%
Chemical Reviews	Chemical Reviews, 1, 2.56% Chemical Reviews 1 публикация, 2.56%
Chemical Science	Chemical Science, 1, 2.56% Chemical Science 1 публикация, 2.56%
ACS Omega	ACS Omega, 1, 2.56% ACS Omega 1 публикация, 2.56%
Journal of Organic Chemistry	Journal of Organic Chemistry, 1, 2.56% Journal of Organic Chemistry 1 публикация, 2.56%
Reaction Chemistry and Engineering	Reaction Chemistry and Engineering, 1, 2.56% Reaction Chemistry and Engineering 1 публикация, 2.56%
Chemical Communications	Chemical Communications, 1, 2.56% Chemical Communications 1 публикация, 2.56%
Analytical Chemistry Letters	Analytical Chemistry Letters, 1, 2.56% Analytical Chemistry Letters 1 публикация, 2.56%
Chemistry International	Chemistry International, 1, 2.56% Chemistry International 1 публикация, 2.56%
Topics in Heterocyclic Chemistry	Topics in Heterocyclic Chemistry, 1, 2.56% Topics in Heterocyclic Chemistry 1 публикация, 2.56%
European Journal of Medicinal Chemistry	European Journal of Medicinal Chemistry, 1, 2.56% European Journal of Medicinal Chemistry 1 публикация, 2.56%
Computer Aided Chemical Engineering	Computer Aided Chemical Engineering, 1, 2.56% Computer Aided Chemical Engineering 1 публикация, 2.56%
AICHE Journal	AICHE Journal, 1, 2.56% AICHE Journal 1 публикация, 2.56%
	1 2 3 4

Издатели

	1 2 3 4 5 6 7 8
Elsevier	Elsevier, 8, 20.51% Elsevier 8 публикаций, 20.51%
American Chemical Society (ACS)	American Chemical Society (ACS), 8, 20.51% American Chemical Society (ACS) 8 публикаций, 20.51%
Wiley	Wiley, 7, 17.95% Wiley 7 публикаций, 17.95%
Springer Nature	Springer Nature, 5, 12.82% Springer Nature 5 публикаций, 12.82%
Royal Society of Chemistry (RSC)	Royal Society of Chemistry (RSC), 5, 12.82% Royal Society of Chemistry (RSC) 5 публикаций, 12.82%
Akademiai Kiado	Akademiai Kiado, 3, 7.69% Akademiai Kiado 3 публикации, 7.69%
MDPI	MDPI, 1, 2.56% MDPI 1 публикация, 2.56%
Taylor & Francis	Taylor & Francis, 1, 2.56% Taylor & Francis 1 публикация, 2.56%
Walter de Gruyter	Walter de Gruyter, 1, 2.56% Walter de Gruyter 1 публикация, 2.56%
	1 2 3 4 5 6 7 8

Мы не учитываем публикации, у которых нет DOI.
Статистика публикаций обновляется еженедельно.

Вы ученый?

Создайте профиль, чтобы получать персональные рекомендации коллег, конференций и новых статей.

Войти с ORCID

Метрики

Цитировать

ГОСТ |

Цитировать

ГОСТ Скопировать

Borukhova S. et al. From alcohol to 1,2,3-triazole via a multi-step continuous-flow synthesis of a rufinamide precursor // Green Chemistry. 2016. Vol. 18. No. 18. pp. 4947-4953.

ГОСТ со всеми авторами (до 50) Скопировать

Borukhova S., Noel T. R., Metten B., De Vos E., Hessel V. From alcohol to 1,2,3-triazole via a multi-step continuous-flow synthesis of a rufinamide precursor // Green Chemistry. 2016. Vol. 18. No. 18. pp. 4947-4953.

RIS |

Цитировать

RIS Скопировать

TY - JOUR

DO - 10.1039/c6gc01133k

UR - https://doi.org/10.1039/c6gc01133k

TI - From alcohol to 1,2,3-triazole via a multi-step continuous-flow synthesis of a rufinamide precursor

T2 - Green Chemistry

AU - Borukhova, Svetlana

AU - Noel, Timothy R.

AU - Metten, Bert

AU - De Vos, Eric

AU - Hessel, Volker

PY - 2016

DA - 2016/05/27

PB - Royal Society of Chemistry (RSC)

SP - 4947-4953

IS - 18

VL - 18

SN - 1463-9262

SN - 1463-9270

ER -

BibTex |

Цитировать

BibTex (до 50 авторов) Скопировать

@article{2016_Borukhova,

author = {Svetlana Borukhova and Timothy R. Noel and Bert Metten and Eric De Vos and Volker Hessel},

title = {From alcohol to 1,2,3-triazole via a multi-step continuous-flow synthesis of a rufinamide precursor},

journal = {Green Chemistry},

year = {2016},

volume = {18},

publisher = {Royal Society of Chemistry (RSC)},

month = {may},

url = {https://doi.org/10.1039/c6gc01133k},

number = {18},

pages = {4947--4953},

doi = {10.1039/c6gc01133k}

}

MLA

Цитировать

MLA Скопировать

Borukhova, Svetlana, et al. “From alcohol to 1,2,3-triazole via a multi-step continuous-flow synthesis of a rufinamide precursor.” Green Chemistry, vol. 18, no. 18, May. 2016, pp. 4947-4953. https://doi.org/10.1039/c6gc01133k.