File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

BielawskiChristopher W

Bielawski, Christopher W.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Reductive generation of stable, five-membered N,N '-diamidocarbenes

Author(s)
Moerdyk, Jonathan P.Bielawski, Christopher W.
Issued Date
2014
DOI
10.1039/c4cc00846d
URI
https://scholarworks.unist.ac.kr/handle/201301/31473
Fulltext
https://pubs.rsc.org/en/content/articlelanding/2014/CC/c4cc00846d#!divAbstract
Citation
CHEMICAL COMMUNICATIONS, v.50, no.35, pp.4551 - 4553
Abstract
The synthesis of the first stable, five-membered N,N'-diamidocarbenes (DACs), including a differentially N-substituted derivative, was achieved via the reduction of a geminal dichloride precursor using potassium. Key differences between the reactivity of the five-membered DACs and their six-membered congeners were observed, including an ability to insert into electron-rich C-H bonds.
Publisher
ROYAL SOC CHEMISTRY
ISSN
1359-7345
Keyword
N-HETEROCYCLIC CARBENESACTIVATIONAMMONIAAMINOCOMPLEXESBACKBONEPRECURSORSREACTIVITYVERSATILEALKYL

qrcode

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