Organic and Biomolecular Chemistry

, том 14 , издание 1 , страницы 122-130

One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination

Тип публикации: Journal Article

Дата публикации: 2016-01-01

Royal Society of Chemistry (RSC)

Organic and Biomolecular Chemistry

scimago Q2

wos Q2

white level БС1

SJR: 0.6

CiteScore: 5.2

Impact factor: 2.7

ISSN: 14770520, 14770539

DOI: 10.1039/c5ob01952d

Скопировать DOI

PubMed ID: 26542026

Organic Chemistry

Biochemistry

Physical and Theoretical Chemistry

Краткое описание

We have developed a highly efficient synthetic route to carbazoles that employs sequential C–C/C–N bond formation via Suzuki cross-coupling and Cadogan cyclization. The developed method is compatible with electron neutral, rich or deficient substrates. The synthetic utility of this method was demonstrated by the concise syntheses of four natural products.

Для доступа к списку цитирований публикации необходимо авторизоваться.

Войти с ORCID

Топ-30

Журналы

	1 2 3 4 5
Journal of Organic Chemistry	Journal of Organic Chemistry, 5, 13.89% Journal of Organic Chemistry 5 публикаций, 13.89%
European Journal of Organic Chemistry	European Journal of Organic Chemistry, 3, 8.33% European Journal of Organic Chemistry 3 публикации, 8.33%
Advanced Synthesis and Catalysis	Advanced Synthesis and Catalysis, 2, 5.56% Advanced Synthesis and Catalysis 2 публикации, 5.56%
ChemistrySelect	ChemistrySelect, 2, 5.56% ChemistrySelect 2 публикации, 5.56%
Green Chemistry	Green Chemistry, 2, 5.56% Green Chemistry 2 публикации, 5.56%
Chemical Communications	Chemical Communications, 2, 5.56% Chemical Communications 2 публикации, 5.56%
Tetrahedron	Tetrahedron, 1, 2.78% Tetrahedron 1 публикация, 2.78%
Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy	Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 1, 2.78% Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy 1 публикация, 2.78%
Tetrahedron Letters	Tetrahedron Letters, 1, 2.78% Tetrahedron Letters 1 публикация, 2.78%
ChemInform	ChemInform, 1, 2.78% ChemInform 1 публикация, 2.78%
Bulletin of the Korean Chemical Society	Bulletin of the Korean Chemical Society, 1, 2.78% Bulletin of the Korean Chemical Society 1 публикация, 2.78%
Physical Chemistry Chemical Physics	Physical Chemistry Chemical Physics, 1, 2.78% Physical Chemistry Chemical Physics 1 публикация, 2.78%
Progress in Heterocyclic Chemistry	Progress in Heterocyclic Chemistry, 1, 2.78% Progress in Heterocyclic Chemistry 1 публикация, 2.78%
Synthesis	Synthesis, 1, 2.78% Synthesis 1 публикация, 2.78%
Advances in Heterocyclic Chemistry	Advances in Heterocyclic Chemistry, 1, 2.78% Advances in Heterocyclic Chemistry 1 публикация, 2.78%
Synlett	Synlett, 1, 2.78% Synlett 1 публикация, 2.78%
Organic and Biomolecular Chemistry	Organic and Biomolecular Chemistry, 1, 2.78% Organic and Biomolecular Chemistry 1 публикация, 2.78%
Chemical Science	Chemical Science, 1, 2.78% Chemical Science 1 публикация, 2.78%
ACS Sustainable Chemistry and Engineering	ACS Sustainable Chemistry and Engineering, 1, 2.78% ACS Sustainable Chemistry and Engineering 1 публикация, 2.78%
Organic Chemistry Frontiers	Organic Chemistry Frontiers, 1, 2.78% Organic Chemistry Frontiers 1 публикация, 2.78%
Russian Chemical Reviews	Russian Chemical Reviews, 1, 2.78% Russian Chemical Reviews 1 публикация, 2.78%
Current Organic Chemistry	Current Organic Chemistry, 1, 2.78% Current Organic Chemistry 1 публикация, 2.78%
Natural Product Communications	Natural Product Communications, 1, 2.78% Natural Product Communications 1 публикация, 2.78%
Chinese Chemical Letters	Chinese Chemical Letters, 1, 2.78% Chinese Chemical Letters 1 публикация, 2.78%
Journal of Catalysis	Journal of Catalysis, 1, 2.78% Journal of Catalysis 1 публикация, 2.78%
	1 2 3 4 5

Издатели

	2 4 6 8 10
Wiley	Wiley, 10, 27.78% Wiley 10 публикаций, 27.78%
Royal Society of Chemistry (RSC)	Royal Society of Chemistry (RSC), 8, 22.22% Royal Society of Chemistry (RSC) 8 публикаций, 22.22%
Elsevier	Elsevier, 7, 19.44% Elsevier 7 публикаций, 19.44%
American Chemical Society (ACS)	American Chemical Society (ACS), 6, 16.67% American Chemical Society (ACS) 6 публикаций, 16.67%
Georg Thieme Verlag KG	Georg Thieme Verlag KG, 2, 5.56% Georg Thieme Verlag KG 2 публикации, 5.56%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii	Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii, 1, 2.78% Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii 1 публикация, 2.78%
Bentham Science Publishers Ltd.	Bentham Science Publishers Ltd., 1, 2.78% Bentham Science Publishers Ltd. 1 публикация, 2.78%
SAGE	SAGE, 1, 2.78% SAGE 1 публикация, 2.78%
	2 4 6 8 10

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

Goo D. Y., Goo D., Woo S. K. One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination // Organic and Biomolecular Chemistry. 2016. Vol. 14. No. 1. pp. 122-130.

ГОСТ со всеми авторами (до 50) Скопировать

Goo D. Y., Goo D., Woo S. K. One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination // Organic and Biomolecular Chemistry. 2016. Vol. 14. No. 1. pp. 122-130.

RIS |

Цитировать

RIS Скопировать

TY - JOUR

DO - 10.1039/c5ob01952d

UR - https://doi.org/10.1039/c5ob01952d

TI - One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination

T2 - Organic and Biomolecular Chemistry

AU - Goo, Deuk Young

AU - Goo, Deuk-Young

AU - Woo, Sang Kook

PY - 2016

DA - 2016/01/01

PB - Royal Society of Chemistry (RSC)

SP - 122-130

IS - 1

VL - 14

PMID - 26542026

SN - 1477-0520

SN - 1477-0539

ER -

BibTex |

Цитировать

BibTex (до 50 авторов) Скопировать

@article{2016_Goo,

author = {Deuk Young Goo and Deuk-Young Goo and Sang Kook Woo},

title = {One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination},

journal = {Organic and Biomolecular Chemistry},

year = {2016},

volume = {14},

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

month = {jan},

url = {https://doi.org/10.1039/c5ob01952d},

number = {1},

pages = {122--130},

doi = {10.1039/c5ob01952d}

}

MLA

Цитировать

MLA Скопировать

Goo, Deuk Young, et al. “One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination.” Organic and Biomolecular Chemistry, vol. 14, no. 1, Jan. 2016, pp. 122-130. https://doi.org/10.1039/c5ob01952d.