Direct formation of 4,5-disubstituted carbazoles via regioselective dilithiation

Research output: Contribution to journalArticlepeer-review

Standard

Direct formation of 4,5-disubstituted carbazoles via regioselective dilithiation. / Pocock, Ian A; Alotaibi, Alya M; Jagdev, Kesar; Prior, Connor; Burgess, Gregory R; Male, Louise; Grainger, Richard S.

In: Chemical communications (Cambridge, England), Vol. 57, No. 59, 28.07.2021, p. 7252-7255.

Research output: Contribution to journalArticlepeer-review

Harvard

APA

Vancouver

Author

Pocock, Ian A ; Alotaibi, Alya M ; Jagdev, Kesar ; Prior, Connor ; Burgess, Gregory R ; Male, Louise ; Grainger, Richard S. / Direct formation of 4,5-disubstituted carbazoles via regioselective dilithiation. In: Chemical communications (Cambridge, England). 2021 ; Vol. 57, No. 59. pp. 7252-7255.

Bibtex

@article{1f867d9c9b1e41dcb249f61490ee3fc3,
title = "Direct formation of 4,5-disubstituted carbazoles via regioselective dilithiation",
abstract = "Carbazoles are widely exploited for their interesting photophysical and electronic properties, however bay (4,5-) functionalization is challenging, and previously inaccessible through carbazole C-H activation. We report a simple methodology which introduces a range of versatile 4,5-functionality, enabling the wider investigation of ring annulation and close proximity effects on carbazole properties.",
author = "Pocock, {Ian A} and Alotaibi, {Alya M} and Kesar Jagdev and Connor Prior and Burgess, {Gregory R} and Louise Male and Grainger, {Richard S}",
note = "Funding Information: We thank the Leverhulme Trust (RPG-2017-260), Prince Sattam bin Abdulaziz University, Saudi Arabia, and EPSRC (EP/M508202/1, EP/N509590/1) for funding.",
year = "2021",
month = jul,
day = "28",
doi = "10.1039/d1cc02892h",
language = "English",
volume = "57",
pages = "7252--7255",
journal = "Chemical Communications ",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
number = "59",

}

RIS

TY - JOUR

T1 - Direct formation of 4,5-disubstituted carbazoles via regioselective dilithiation

AU - Pocock, Ian A

AU - Alotaibi, Alya M

AU - Jagdev, Kesar

AU - Prior, Connor

AU - Burgess, Gregory R

AU - Male, Louise

AU - Grainger, Richard S

N1 - Funding Information: We thank the Leverhulme Trust (RPG-2017-260), Prince Sattam bin Abdulaziz University, Saudi Arabia, and EPSRC (EP/M508202/1, EP/N509590/1) for funding.

PY - 2021/7/28

Y1 - 2021/7/28

N2 - Carbazoles are widely exploited for their interesting photophysical and electronic properties, however bay (4,5-) functionalization is challenging, and previously inaccessible through carbazole C-H activation. We report a simple methodology which introduces a range of versatile 4,5-functionality, enabling the wider investigation of ring annulation and close proximity effects on carbazole properties.

AB - Carbazoles are widely exploited for their interesting photophysical and electronic properties, however bay (4,5-) functionalization is challenging, and previously inaccessible through carbazole C-H activation. We report a simple methodology which introduces a range of versatile 4,5-functionality, enabling the wider investigation of ring annulation and close proximity effects on carbazole properties.

UR - http://www.scopus.com/inward/record.url?scp=85111030269&partnerID=8YFLogxK

U2 - 10.1039/d1cc02892h

DO - 10.1039/d1cc02892h

M3 - Article

C2 - 34190745

VL - 57

SP - 7252

EP - 7255

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 59

ER -