Direct acylation of N-benzyltriflamides from the alcohol oxidation level via palladium-catalyzed C-H bond activation

Jihye Park; Aejin Kim; Satyasheel Sharma; Minyoung Kim; Eonjeong Park; Yukyoung Jeon; Youngil Lee; Jong Hwan Kwak; Young Hoon Jung; In Su Kim

doi:10.1039/c3ob40140e

Direct acylation of N-benzyltriflamides from the alcohol oxidation level via palladium-catalyzed C-H bond activation

Jihye Park
, Aejin Kim
, Satyasheel Sharma
, Minyoung Kim
, Eonjeong Park
, Yukyoung Jeon
, Youngil Lee
, Jong Hwan Kwak
, Young Hoon Jung
, In Su Kim

Department of Pharmacy

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

55 Scopus citations

Abstract

A palladium-catalyzed ortho-acylation of N-benzyltriflamides from the alcohol oxidation level via C-H bond activation is described. These transformations have been applied to a wide range of substrates, and typically proceed with excellent levels of chemoselectivity and with high functional group tolerance.

Original language	English
Pages (from-to)	2766-2771
Number of pages	6
Journal	Organic and Biomolecular Chemistry
Volume	11
Issue number	17
DOIs	https://doi.org/10.1039/c3ob40140e
State	Published - 7 May 2013

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abstract = "A palladium-catalyzed ortho-acylation of N-benzyltriflamides from the alcohol oxidation level via C-H bond activation is described. These transformations have been applied to a wide range of substrates, and typically proceed with excellent levels of chemoselectivity and with high functional group tolerance.",

author = "Jihye Park and Aejin Kim and Satyasheel Sharma and Minyoung Kim and Eonjeong Park and Yukyoung Jeon and Youngil Lee and Kwak, \{Jong Hwan\} and Jung, \{Young Hoon\} and Kim, \{In Su\}",

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T1 - Direct acylation of N-benzyltriflamides from the alcohol oxidation level via palladium-catalyzed C-H bond activation

AU - Park, Jihye

AU - Kim, Aejin

AU - Sharma, Satyasheel

AU - Kim, Minyoung

AU - Park, Eonjeong

AU - Jeon, Yukyoung

AU - Lee, Youngil

AU - Kwak, Jong Hwan

AU - Jung, Young Hoon

AU - Kim, In Su

PY - 2013/5/7

Y1 - 2013/5/7

N2 - A palladium-catalyzed ortho-acylation of N-benzyltriflamides from the alcohol oxidation level via C-H bond activation is described. These transformations have been applied to a wide range of substrates, and typically proceed with excellent levels of chemoselectivity and with high functional group tolerance.

AB - A palladium-catalyzed ortho-acylation of N-benzyltriflamides from the alcohol oxidation level via C-H bond activation is described. These transformations have been applied to a wide range of substrates, and typically proceed with excellent levels of chemoselectivity and with high functional group tolerance.

UR - https://www.scopus.com/pages/publications/84875859599

U2 - 10.1039/c3ob40140e

DO - 10.1039/c3ob40140e

M3 - Article

C2 - 23493982

AN - SCOPUS:84875859599

SN - 1477-0520

VL - 11

SP - 2766

EP - 2771

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

IS - 17

ER -

Direct acylation of N-benzyltriflamides from the alcohol oxidation level via palladium-catalyzed C-H bond activation

Abstract

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