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Selective oxidative intermolecular carbosulphenylation of aryl alkenes with thiols and nucleophilesviaa 1,2-dithioethane intermediate. / Wang, Yuna; Qi, Zaojuan; Niu, Yanning и др.

в: Chemical Communications, Том 57, № 61, 29.07.2021, стр. 7533-7536.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Wang, Y, Qi, Z, Niu, Y, Feng, H, Benassi, E & Qian, B 2021, 'Selective oxidative intermolecular carbosulphenylation of aryl alkenes with thiols and nucleophilesviaa 1,2-dithioethane intermediate', Chemical Communications, Том. 57, № 61, стр. 7533-7536. https://doi.org/10.1039/d1cc02517a

APA

Wang, Y., Qi, Z., Niu, Y., Feng, H., Benassi, E., & Qian, B. (2021). Selective oxidative intermolecular carbosulphenylation of aryl alkenes with thiols and nucleophilesviaa 1,2-dithioethane intermediate. Chemical Communications, 57(61), 7533-7536. https://doi.org/10.1039/d1cc02517a

Vancouver

Wang Y, Qi Z, Niu Y, Feng H, Benassi E, Qian B. Selective oxidative intermolecular carbosulphenylation of aryl alkenes with thiols and nucleophilesviaa 1,2-dithioethane intermediate. Chemical Communications. 2021 июль 29;57(61):7533-7536. doi: 10.1039/d1cc02517a

Author

Wang, Yuna ; Qi, Zaojuan ; Niu, Yanning и др. / Selective oxidative intermolecular carbosulphenylation of aryl alkenes with thiols and nucleophilesviaa 1,2-dithioethane intermediate. в: Chemical Communications. 2021 ; Том 57, № 61. стр. 7533-7536.

BibTeX

@article{23c90f9a97bf406c821ea94e288ef213,
title = "Selective oxidative intermolecular carbosulphenylation of aryl alkenes with thiols and nucleophilesviaa 1,2-dithioethane intermediate",
abstract = "A periodate lithium-oxidized difunctionalisation of aryl alkenes with thiols and electron-rich aromatics was achieved, selectively affording more than thirty carbosulphenylated products. Both experiments and quantum chemical calculations demonstrated the radical-polar nature of the processes, and that 1,2-dithioethane and thiiranium ions might play the role of intermediates.",
author = "Yuna Wang and Zaojuan Qi and Yanning Niu and Hua Feng and Enrico Benassi and Bo Qian",
note = "Publisher Copyright: {\textcopyright} The Royal Society of Chemistry 2021.",
year = "2021",
month = jul,
day = "29",
doi = "10.1039/d1cc02517a",
language = "English",
volume = "57",
pages = "7533--7536",
journal = "Chemical Communications",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
number = "61",

}

RIS

TY - JOUR

T1 - Selective oxidative intermolecular carbosulphenylation of aryl alkenes with thiols and nucleophilesviaa 1,2-dithioethane intermediate

AU - Wang, Yuna

AU - Qi, Zaojuan

AU - Niu, Yanning

AU - Feng, Hua

AU - Benassi, Enrico

AU - Qian, Bo

N1 - Publisher Copyright: © The Royal Society of Chemistry 2021.

PY - 2021/7/29

Y1 - 2021/7/29

N2 - A periodate lithium-oxidized difunctionalisation of aryl alkenes with thiols and electron-rich aromatics was achieved, selectively affording more than thirty carbosulphenylated products. Both experiments and quantum chemical calculations demonstrated the radical-polar nature of the processes, and that 1,2-dithioethane and thiiranium ions might play the role of intermediates.

AB - A periodate lithium-oxidized difunctionalisation of aryl alkenes with thiols and electron-rich aromatics was achieved, selectively affording more than thirty carbosulphenylated products. Both experiments and quantum chemical calculations demonstrated the radical-polar nature of the processes, and that 1,2-dithioethane and thiiranium ions might play the role of intermediates.

UR - http://www.scopus.com/inward/record.url?scp=85111604226&partnerID=8YFLogxK

U2 - 10.1039/d1cc02517a

DO - 10.1039/d1cc02517a

M3 - Article

C2 - 34236369

AN - SCOPUS:85111604226

VL - 57

SP - 7533

EP - 7536

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 61

ER -

ID: 29281809