Nickel-catalyzed: Exo -selective hydroacylation/Suzuki cross-coupling reaction

Shao Chi Lee; Lin Guo; Magnus Rueping

doi:10.1039/c9cc07558e

Nickel-catalyzed: Exo -selective hydroacylation/Suzuki cross-coupling reaction

Shao Chi Lee
, Lin Guo
, Magnus Rueping^*

^*Corresponding author for this work

RWTH Aachen University
King Abdullah University of Science and Technology

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

14 Scopus citations

Abstract

The first nickel-catalyzed intramolecular hydroacylation/Suzuki cross coupling cascade of o-allylbenzaldehydes with a broad range of phenylboronic acid neopentyl glycol esters has been developed. This strategy shows high regioselectivity and step economy in the construction of two C-C bonds via aldehyde C-H bond activation, affording valuable indanones with high efficiency.

Original language	English
Pages (from-to)	14984-14987
Number of pages	4
Journal	Chemical Communications
Volume	55
Issue number	99
DOIs	https://doi.org/10.1039/c9cc07558e
State	Published - 2019
Externally published	Yes

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title = "Nickel-catalyzed: Exo -selective hydroacylation/Suzuki cross-coupling reaction",

abstract = "The first nickel-catalyzed intramolecular hydroacylation/Suzuki cross coupling cascade of o-allylbenzaldehydes with a broad range of phenylboronic acid neopentyl glycol esters has been developed. This strategy shows high regioselectivity and step economy in the construction of two C-C bonds via aldehyde C-H bond activation, affording valuable indanones with high efficiency.",

author = "Lee, \{Shao Chi\} and Lin Guo and Magnus Rueping",

note = "Publisher Copyright: This journal is {\textcopyright} The Royal Society of Chemistry.",

year = "2019",

doi = "10.1039/c9cc07558e",

language = "英语",

volume = "55",

pages = "14984--14987",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

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TY - JOUR

T1 - Nickel-catalyzed

T2 - Exo -selective hydroacylation/Suzuki cross-coupling reaction

AU - Lee, Shao Chi

AU - Guo, Lin

AU - Rueping, Magnus

N1 - Publisher Copyright: This journal is © The Royal Society of Chemistry.

PY - 2019

Y1 - 2019

N2 - The first nickel-catalyzed intramolecular hydroacylation/Suzuki cross coupling cascade of o-allylbenzaldehydes with a broad range of phenylboronic acid neopentyl glycol esters has been developed. This strategy shows high regioselectivity and step economy in the construction of two C-C bonds via aldehyde C-H bond activation, affording valuable indanones with high efficiency.

AB - The first nickel-catalyzed intramolecular hydroacylation/Suzuki cross coupling cascade of o-allylbenzaldehydes with a broad range of phenylboronic acid neopentyl glycol esters has been developed. This strategy shows high regioselectivity and step economy in the construction of two C-C bonds via aldehyde C-H bond activation, affording valuable indanones with high efficiency.

UR - https://www.scopus.com/pages/publications/85076330656

U2 - 10.1039/c9cc07558e

DO - 10.1039/c9cc07558e

M3 - 文章

C2 - 31777905

AN - SCOPUS:85076330656

SN - 1359-7345

VL - 55

SP - 14984

EP - 14987

JO - Chemical Communications

JF - Chemical Communications

IS - 99

ER -

Nickel-catalyzed: Exo -selective hydroacylation/Suzuki cross-coupling reaction

Abstract

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