Chemistry Letters

, том 10 , издание 7 , страницы 869-872

SYNTHESIS OF PYRROLE DERIVATIVES VIA DEOXYGENATION OF 4H-1,2-OXAZINES BY IRON CARBONYLS

Тип публикации: Journal Article

Дата публикации: 1981-07-05

Oxford University Press

Chemistry Letters

SCImago Q3

WOS Q4

БС2

SJR: 0.276

CiteScore: 1.8

Impact factor: 1.1

ISSN: 03667022, 13480715

DOI: 10.1246/cl.1981.869

Скопировать DOI

General Chemistry

Краткое описание

The reaction of 5,6-dihydro-4H-1,2-oxazines, which are derived from α-bromooximes and enamines, with iron carbonyl complexes such as Fe3(CO)12 and (C2H5)3NH[HFe3(CO)11] gives pyrrole derivatives in high yields, accompaning deoxygenation from the oxazines. The pyrroles are also obtained by an one-pot reaction using α-bromooximes, enamines and iron carbonyls.

Для доступа к списку цитирований публикации необходимо авторизоваться.

Войти с ORCID

Для доступа к списку профилей, цитирующих публикацию, необходимо авторизоваться.

Войти с ORCID

Топ-30

Журналы

	1 2 3
European Journal of Organic Chemistry	European Journal of Organic Chemistry, 3, 12% European Journal of Organic Chemistry 3 публикации, 12%
Chemistry Letters	Chemistry Letters, 1, 4% Chemistry Letters 1 публикация, 4%
Proceedings of the Indian Academy of Sciences - Section A	Proceedings of the Indian Academy of Sciences - Section A, 1, 4% Proceedings of the Indian Academy of Sciences - Section A 1 публикация, 4%
Chemistry of Heterocyclic Compounds	Chemistry of Heterocyclic Compounds, 1, 4% Chemistry of Heterocyclic Compounds 1 публикация, 4%
Russian Chemical Reviews	Russian Chemical Reviews, 1, 4% Russian Chemical Reviews 1 публикация, 4%
Tetrahedron	Tetrahedron, 1, 4% Tetrahedron 1 публикация, 4%
Tetrahedron Letters	Tetrahedron Letters, 1, 4% Tetrahedron Letters 1 публикация, 4%
Chemischer Informationsdienst	Chemischer Informationsdienst, 1, 4% Chemischer Informationsdienst 1 публикация, 4%
Journal of Heterocyclic Chemistry	Journal of Heterocyclic Chemistry, 1, 4% Journal of Heterocyclic Chemistry 1 публикация, 4%
Chemical Biology and Drug Design	Chemical Biology and Drug Design, 1, 4% Chemical Biology and Drug Design 1 публикация, 4%
Chemical Reviews	Chemical Reviews, 1, 4% Chemical Reviews 1 публикация, 4%
Organic Letters	Organic Letters, 1, 4% Organic Letters 1 публикация, 4%
Organic and Biomolecular Chemistry	Organic and Biomolecular Chemistry, 1, 4% Organic and Biomolecular Chemistry 1 публикация, 4%
Chemical Communications	Chemical Communications, 1, 4% Chemical Communications 1 публикация, 4%
Organic Preparations and Procedures International	Organic Preparations and Procedures International, 1, 4% Organic Preparations and Procedures International 1 публикация, 4%
Cumulative Index of Heterocyclic Systems	Cumulative Index of Heterocyclic Systems, 1, 4% Cumulative Index of Heterocyclic Systems 1 публикация, 4%
Organic Chemistry	Organic Chemistry, 1, 4% Organic Chemistry 1 публикация, 4%
Heterocycles	Heterocycles, 1, 4% Heterocycles 1 публикация, 4%
Organic Chemistry Frontiers	Organic Chemistry Frontiers, 1, 4% Organic Chemistry Frontiers 1 публикация, 4%
	1 2 3

Издатели

	1 2 3 4 5 6 7
Elsevier	Elsevier, 7, 28% Elsevier 7 публикаций, 28%
Wiley	Wiley, 7, 28% Wiley 7 публикаций, 28%
Royal Society of Chemistry (RSC)	Royal Society of Chemistry (RSC), 3, 12% Royal Society of Chemistry (RSC) 3 публикации, 12%
Springer Nature	Springer Nature, 2, 8% Springer Nature 2 публикации, 8%
American Chemical Society (ACS)	American Chemical Society (ACS), 2, 8% American Chemical Society (ACS) 2 публикации, 8%
Oxford University Press	Oxford University Press, 1, 4% Oxford University Press 1 публикация, 4%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii	Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii, 1, 4% Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii 1 публикация, 4%
Taylor & Francis	Taylor & Francis, 1, 4% Taylor & Francis 1 публикация, 4%
The Japan Institute of Heterocyclic Chemistry	The Japan Institute of Heterocyclic Chemistry, 1, 4% The Japan Institute of Heterocyclic Chemistry 1 публикация, 4%
	1 2 3 4 5 6 7

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

Nakanishi S. et al. SYNTHESIS OF PYRROLE DERIVATIVES VIA DEOXYGENATION OF 4H-1,2-OXAZINES BY IRON CARBONYLS // Chemistry Letters. 1981. Vol. 10. No. 7. pp. 869-872.

ГОСТ со всеми авторами (до 50) Скопировать

Nakanishi S., Shirai Y., TAKAHASHI K., Otsuji Y. SYNTHESIS OF PYRROLE DERIVATIVES VIA DEOXYGENATION OF 4H-1,2-OXAZINES BY IRON CARBONYLS // Chemistry Letters. 1981. Vol. 10. No. 7. pp. 869-872.

RIS |

Цитировать

RIS Скопировать

TY - JOUR

DO - 10.1246/cl.1981.869

UR - https://doi.org/10.1246/cl.1981.869

TI - SYNTHESIS OF PYRROLE DERIVATIVES VIA DEOXYGENATION OF 4H-1,2-OXAZINES BY IRON CARBONYLS

T2 - Chemistry Letters

AU - Nakanishi, Saburo

AU - Shirai, Yoshihiro

AU - TAKAHASHI, KENJI

AU - Otsuji, Yoshio

PY - 1981

DA - 1981/07/05

PB - Oxford University Press

SP - 869-872

IS - 7

VL - 10

SN - 0366-7022

SN - 1348-0715

ER -

BibTex |

Цитировать

BibTex (до 50 авторов) Скопировать

@article{1981_Nakanishi,

author = {Saburo Nakanishi and Yoshihiro Shirai and KENJI TAKAHASHI and Yoshio Otsuji},

title = {SYNTHESIS OF PYRROLE DERIVATIVES VIA DEOXYGENATION OF 4H-1,2-OXAZINES BY IRON CARBONYLS},

journal = {Chemistry Letters},

year = {1981},

volume = {10},

publisher = {Oxford University Press},

month = {jul},

url = {https://doi.org/10.1246/cl.1981.869},

number = {7},

pages = {869--872},

doi = {10.1246/cl.1981.869}

}

MLA

Цитировать

MLA Скопировать

Nakanishi, Saburo, et al. “SYNTHESIS OF PYRROLE DERIVATIVES VIA DEOXYGENATION OF 4H-1,2-OXAZINES BY IRON CARBONYLS.” Chemistry Letters, vol. 10, no. 7, Jul. 1981, pp. 869-872. https://doi.org/10.1246/cl.1981.869.

Издатель

Oxford University Press

Журнал

Chemistry Letters

SCImago Q3

WOS Q4

БС2

SJR

0.276

CiteScore

1.8

Impact factor