Royal Society of Chemistry (RSC)
Organic and Biomolecular Chemistry
,  том 17 ,  издание 20 ,  страницы 5029-5037

Nickel(ii)-catalyzed C(sp2)–H sulfuration/annulation with elemental sulfur: selective access to benzoisothiazolones

Тип публикации: Journal Article
Дата публикации: 2019-04-27
Royal Society of Chemistry (RSC)
SCImago Q2
WOS Q2
БС1
SJR: 0.475
CiteScore: 5.2
Impact factor: 2.7
ISSN: 14770520, 14770539
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
The first nickel(II)-catalyzed direct sulfuration/annulation of C(sp2)–H bonds with elemental sulfur has been achieved by using 2-amino alkylbenzimidazole (MBIP-amine) as a N,N-bidentate directing group. This strategy tolerates a wide range of functional groups, furnishing structurally diverse benzoisothiazolone derivatives with benzimidazole skeletons in moderate to excellent yields in a simple and efficient way.
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Guo J. R. et al. Nickel(ii)-catalyzed C(sp2)–H sulfuration/annulation with elemental sulfur: selective access to benzoisothiazolones // Organic and Biomolecular Chemistry. 2019. Vol. 17. No. 20. pp. 5029-5037.
ГОСТ со всеми авторами (до 50) Скопировать
Guo J. R., Guo J., Gong J., Song M. Nickel(ii)-catalyzed C(sp2)–H sulfuration/annulation with elemental sulfur: selective access to benzoisothiazolones // Organic and Biomolecular Chemistry. 2019. Vol. 17. No. 20. pp. 5029-5037.
RIS |
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TY - JOUR
DO - 10.1039/c9ob00449a
UR - https://xlink.rsc.org/?DOI=C9OB00449A
TI - Nickel(ii)-catalyzed C(sp2)–H sulfuration/annulation with elemental sulfur: selective access to benzoisothiazolones
T2 - Organic and Biomolecular Chemistry
AU - Guo, Jun Ru
AU - Guo, Jun-Ru
AU - Gong, Junfang
AU - Song, Maoping
PY - 2019
DA - 2019/04/27
PB - Royal Society of Chemistry (RSC)
SP - 5029-5037
IS - 20
VL - 17
PMID - 31045200
SN - 1477-0520
SN - 1477-0539
ER -
BibTex |
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@article{2019_Guo,
author = {Jun Ru Guo and Jun-Ru Guo and Junfang Gong and Maoping Song},
title = {Nickel(ii)-catalyzed C(sp2)–H sulfuration/annulation with elemental sulfur: selective access to benzoisothiazolones},
journal = {Organic and Biomolecular Chemistry},
year = {2019},
volume = {17},
publisher = {Royal Society of Chemistry (RSC)},
month = {apr},
url = {https://xlink.rsc.org/?DOI=C9OB00449A},
number = {20},
pages = {5029--5037},
doi = {10.1039/c9ob00449a}
}
MLA
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Guo, Jun Ru, et al. “Nickel(ii)-catalyzed C(sp2)–H sulfuration/annulation with elemental sulfur: selective access to benzoisothiazolones.” Organic and Biomolecular Chemistry, vol. 17, no. 20, Apr. 2019, pp. 5029-5037. https://xlink.rsc.org/?DOI=C9OB00449A.
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