Insertion of carbon monoxide into an unsymmetrical diborene to form an oxaborirane
The insertion of carbon monoxide (CO) into an unsymmetrical diborene, concomitant with B-O bond formation under ambient conditions, gives an oxaborirane species. A similar insertion reaction with isocyanide, the isoelectronic species of CO, generates azaboriridine derivatives.
Saved in:
Main Authors: | , |
---|---|
Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2024
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/174233 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-174233 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-1742332024-03-22T15:31:40Z Insertion of carbon monoxide into an unsymmetrical diborene to form an oxaborirane Zhu, Lizhao Kinjo, Rei School of Chemistry, Chemical Engineering and Biotechnology Chemistry Azaboriridine derivative Carbon monoxide The insertion of carbon monoxide (CO) into an unsymmetrical diborene, concomitant with B-O bond formation under ambient conditions, gives an oxaborirane species. A similar insertion reaction with isocyanide, the isoelectronic species of CO, generates azaboriridine derivatives. National Research Foundation (NRF) Submitted/Accepted version We are grateful to Nanyang Technological University (NTU), Nippon Shokubai, and the National Research Foundation, Singapore (NRF-NRFI07-2021-0002) for financial support. 2024-03-22T05:22:29Z 2024-03-22T05:22:29Z 2023 Journal Article Zhu, L. & Kinjo, R. (2023). Insertion of carbon monoxide into an unsymmetrical diborene to form an oxaborirane. Chemical Communications, 59(69), 10436-10439. https://dx.doi.org/10.1039/d3cc02844e 1359-7345 https://hdl.handle.net/10356/174233 10.1039/d3cc02844e 37555354 2-s2.0-85168743371 69 59 10436 10439 en NRF-NRFI07-2021-0002 Chemical Communications © 2023 The Author(s). All rights reserved. This article may be downloaded for personal use only. Any other use requires prior permission of the copyright holder. The Version of Record is available online at http://doi.org/10.1039/D3CC02844E. application/pdf |
institution |
Nanyang Technological University |
building |
NTU Library |
continent |
Asia |
country |
Singapore Singapore |
content_provider |
NTU Library |
collection |
DR-NTU |
language |
English |
topic |
Chemistry Azaboriridine derivative Carbon monoxide |
spellingShingle |
Chemistry Azaboriridine derivative Carbon monoxide Zhu, Lizhao Kinjo, Rei Insertion of carbon monoxide into an unsymmetrical diborene to form an oxaborirane |
description |
The insertion of carbon monoxide (CO) into an unsymmetrical diborene, concomitant with B-O bond formation under ambient conditions, gives an oxaborirane species. A similar insertion reaction with isocyanide, the isoelectronic species of CO, generates azaboriridine derivatives. |
author2 |
School of Chemistry, Chemical Engineering and Biotechnology |
author_facet |
School of Chemistry, Chemical Engineering and Biotechnology Zhu, Lizhao Kinjo, Rei |
format |
Article |
author |
Zhu, Lizhao Kinjo, Rei |
author_sort |
Zhu, Lizhao |
title |
Insertion of carbon monoxide into an unsymmetrical diborene to form an oxaborirane |
title_short |
Insertion of carbon monoxide into an unsymmetrical diborene to form an oxaborirane |
title_full |
Insertion of carbon monoxide into an unsymmetrical diborene to form an oxaborirane |
title_fullStr |
Insertion of carbon monoxide into an unsymmetrical diborene to form an oxaborirane |
title_full_unstemmed |
Insertion of carbon monoxide into an unsymmetrical diborene to form an oxaborirane |
title_sort |
insertion of carbon monoxide into an unsymmetrical diborene to form an oxaborirane |
publishDate |
2024 |
url |
https://hdl.handle.net/10356/174233 |
_version_ |
1794549321574645760 |