Boron-based catalysts for C − C bond‐formation reactions
Because the construction of the C−C bond is one of the most significant reactions in organic chemistry, the development of an efficient strategy has attracted much attention throughout the synthetic community. Among various protocols to form C−C bonds, organoboron compounds are not just limited to s...
Saved in:
Main Authors: | , |
---|---|
Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2020
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/141812 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-141812 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-1418122020-06-11T01:42:08Z Boron-based catalysts for C − C bond‐formation reactions Rao, Bin Kinjo, Rei School of Physical and Mathematical Sciences Science::Chemistry Boranes Boron Because the construction of the C−C bond is one of the most significant reactions in organic chemistry, the development of an efficient strategy has attracted much attention throughout the synthetic community. Among various protocols to form C−C bonds, organoboron compounds are not just limited to stoichiometric reagents, but have also made great achievements as catalysts because of the easy modification of the electronic and steric impacts on the boron center. This review presents recent developments of boron‐based catalysts applied in the field of C−C bond‐formation reactions, which are classified into four kinds on the basis of the type of boron catalyst: 1) highly Lewis acidic borane, B(C6F5)3; 2) organoboron acids, RB(OH)2, and their ester derivatives; 3) borenium ions, (R2BL)X; and 4) other miscellaneous kinds. MOE (Min. of Education, S’pore) 2020-06-11T01:42:08Z 2020-06-11T01:42:08Z 2018 Journal Article Rao, B., & Kinjo, R. (2018). Boron-based catalysts for C − C bond‐formation reactions. Chemistry - An Asian Journal, 13(10), 1279-1292. doi:10.1002/asia.201701796 1861-4728 https://hdl.handle.net/10356/141812 10.1002/asia.201701796 29719122 2-s2.0-85046262615 10 13 1279 1292 en Chemistry - An Asian journal © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. All rights reserved. |
institution |
Nanyang Technological University |
building |
NTU Library |
country |
Singapore |
collection |
DR-NTU |
language |
English |
topic |
Science::Chemistry Boranes Boron |
spellingShingle |
Science::Chemistry Boranes Boron Rao, Bin Kinjo, Rei Boron-based catalysts for C − C bond‐formation reactions |
description |
Because the construction of the C−C bond is one of the most significant reactions in organic chemistry, the development of an efficient strategy has attracted much attention throughout the synthetic community. Among various protocols to form C−C bonds, organoboron compounds are not just limited to stoichiometric reagents, but have also made great achievements as catalysts because of the easy modification of the electronic and steric impacts on the boron center. This review presents recent developments of boron‐based catalysts applied in the field of C−C bond‐formation reactions, which are classified into four kinds on the basis of the type of boron catalyst: 1) highly Lewis acidic borane, B(C6F5)3; 2) organoboron acids, RB(OH)2, and their ester derivatives; 3) borenium ions, (R2BL)X; and 4) other miscellaneous kinds. |
author2 |
School of Physical and Mathematical Sciences |
author_facet |
School of Physical and Mathematical Sciences Rao, Bin Kinjo, Rei |
format |
Article |
author |
Rao, Bin Kinjo, Rei |
author_sort |
Rao, Bin |
title |
Boron-based catalysts for C − C bond‐formation reactions |
title_short |
Boron-based catalysts for C − C bond‐formation reactions |
title_full |
Boron-based catalysts for C − C bond‐formation reactions |
title_fullStr |
Boron-based catalysts for C − C bond‐formation reactions |
title_full_unstemmed |
Boron-based catalysts for C − C bond‐formation reactions |
title_sort |
boron-based catalysts for c − c bond‐formation reactions |
publishDate |
2020 |
url |
https://hdl.handle.net/10356/141812 |
_version_ |
1681057400930435072 |