Cross dehydrogenative coupling strategy for allylation of benzylanilines promoted by DDQ

Ruimei Xiong; Muhammad Ijaz Hussain; Qing Liu; Wen Xia; Yan Xiong

doi:10.1016/j.tet.2019.130798

Cross dehydrogenative coupling strategy for allylation of benzylanilines promoted by DDQ

Ruimei Xiong, Muhammad Ijaz Hussain, Qing Liu, Wen Xia, Yan Xiong

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Abstract

A cross dehydrogenative coupling strategy for allylation of benzylanilines promoted by DDQ is reported, which uses nonmetallic quinone DDQ as an oxidant in the allylation of N-benzylanilines under mild conditions. C–C bond with high selectivity and activity was constructed in this reaction and homoallylic amines were obtained with yields of up to 99%.

Original language	English (US)
Journal	Tetrahedron
Volume	76
Issue number	1
DOIs	https://doi.org/10.1016/j.tet.2019.130798
State	Published - Jan 3 2020
Externally published	Yes

Bibliographical note

Generated from Scopus record by KAUST IRTS on 2023-10-22

Access to Document

10.1016/j.tet.2019.130798

Cite this

@article{b40f2928c275415b8615f44d366d6332,

title = "Cross dehydrogenative coupling strategy for allylation of benzylanilines promoted by DDQ",

abstract = "A cross dehydrogenative coupling strategy for allylation of benzylanilines promoted by DDQ is reported, which uses nonmetallic quinone DDQ as an oxidant in the allylation of N-benzylanilines under mild conditions. C–C bond with high selectivity and activity was constructed in this reaction and homoallylic amines were obtained with yields of up to 99%.",

author = "Ruimei Xiong and Hussain, {Muhammad Ijaz} and Qing Liu and Wen Xia and Yan Xiong",

note = "Generated from Scopus record by KAUST IRTS on 2023-10-22",

year = "2020",

month = jan,

day = "3",

doi = "10.1016/j.tet.2019.130798",

language = "English (US)",

volume = "76",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier Ltd",

number = "1",

}

TY - JOUR

T1 - Cross dehydrogenative coupling strategy for allylation of benzylanilines promoted by DDQ

AU - Xiong, Ruimei

AU - Hussain, Muhammad Ijaz

AU - Liu, Qing

AU - Xia, Wen

AU - Xiong, Yan

N1 - Generated from Scopus record by KAUST IRTS on 2023-10-22

PY - 2020/1/3

Y1 - 2020/1/3

N2 - A cross dehydrogenative coupling strategy for allylation of benzylanilines promoted by DDQ is reported, which uses nonmetallic quinone DDQ as an oxidant in the allylation of N-benzylanilines under mild conditions. C–C bond with high selectivity and activity was constructed in this reaction and homoallylic amines were obtained with yields of up to 99%.

AB - A cross dehydrogenative coupling strategy for allylation of benzylanilines promoted by DDQ is reported, which uses nonmetallic quinone DDQ as an oxidant in the allylation of N-benzylanilines under mild conditions. C–C bond with high selectivity and activity was constructed in this reaction and homoallylic amines were obtained with yields of up to 99%.

UR - https://linkinghub.elsevier.com/retrieve/pii/S0040402019312001

UR - http://www.scopus.com/inward/record.url?scp=85075911709&partnerID=8YFLogxK

U2 - 10.1016/j.tet.2019.130798

DO - 10.1016/j.tet.2019.130798

M3 - Article

SN - 0040-4020

VL - 76

JO - Tetrahedron

JF - Tetrahedron

IS - 1

ER -

Cross dehydrogenative coupling strategy for allylation of benzylanilines promoted by DDQ

Abstract

Bibliographical note

Access to Document

Other files and links

Fingerprint

Cite this