Please use this identifier to cite or link to this item:
https://dspace.ctu.edu.vn/jspui/handle/123456789/103938
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Nguyen, Van Vinh Ha | - |
dc.contributor.author | Nguyen, Thi Thu Ha | - |
dc.contributor.author | Ong, Ngoc Khanh | - |
dc.contributor.author | Dinh, Truc Phuong | - |
dc.contributor.author | Ho, Thanh Nhat | - |
dc.contributor.author | Nguyen, Thanh Tung | - |
dc.date.accessioned | 2024-06-26T07:38:28Z | - |
dc.date.available | 2024-06-26T07:38:28Z | - |
dc.date.issued | 2023 | - |
dc.identifier.issn | 2525-2321 | - |
dc.identifier.uri | https://dspace.ctu.edu.vn/jspui/handle/123456789/103938 | - |
dc.description.abstract | Herein we reported a method for copper pivalate mediated, directed functionalization of ortho C-H bonds in (2- methylthio) aniline benzamides. Diaryl disulfides were used for thiolation, while successful phenoxylation was obtained with phenol as the coupling agent. Our report marks a rare example for flexible transformation of benzamide C(sp²)-H bonds into the corresponding unsymmetrical diaryl ethers and thioethers. | vi_VN |
dc.language.iso | en | vi_VN |
dc.relation.ispartofseries | Vietnam journal of Chemistry;Vol.61, No.02 .- P.204-209 | - |
dc.subject | C-H functionalization | vi_VN |
dc.subject | Copper | vi_VN |
dc.subject | Thiolation | vi_VN |
dc.subject | Phenol | vi_VN |
dc.subject | Directing group | vi_VN |
dc.title | Copper promoted, directed sulfenylation and phenoxylation of benzamide C-H bonds | vi_VN |
dc.type | Article | vi_VN |
Appears in Collections: | Vietnam Journal of Chemistry |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
_file_ Restricted Access | 3.67 MB | Adobe PDF | ||
Your IP: 3.141.25.100 |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.