BROWSE

Related Scientist

Researcher

강택
분자활성 촉매반응 연구단
more info

Iridium-Catalyzed Intermolecular Amidation of sp3 C–H Bonds: Late-Stage Functionalization of an Unactivated Methyl Group Highly Cited Paper

Cited 166 time in webofscience Cited 0 time in scopus
572 Viewed 165 Downloaded
Title
Iridium-Catalyzed Intermolecular Amidation of sp3 C–H Bonds: Late-Stage Functionalization of an Unactivated Methyl Group
Author(s)
Taek Kang; Youngchan Kim; Donggun Lee; Zhen Wang; Suk Bok Chang
Publication Date
2014-03
Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.136, no.11, pp.4141 - 4144
Publisher
AMER CHEMICAL SOC
Abstract
Reported herein is the iridium-catalyzed direct amidation of unactivated sp3 C−H bonds. With sulfonyl and acyl azides as the amino source, the amidation occurs efficiently under mild conditions over a wide range of unactivated methyl groups with high functional group tolerance. This procedure can be successfully applied for the direct introduction of an amino group into complex compounds and thus can serve as a powerful synthetic tool for late-stage C−H functionalization.
URI
https://pr.ibs.re.kr/handle/8788114/1101
ISSN
0002-7863
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > Journal Papers (저널논문)
Files in This Item:
Iridium-Catalyzed Intermolecular Amidation of sp3 C–H Bonds Late-Stage Functionalization of an Unactivated Methyl Group.pdfDownload

qrcode

  • facebook

    twitter

  • Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
해당 아이템을 이메일로 공유하기 원하시면 인증을 거치시기 바랍니다.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse