Rhodium-catalyzed C—H alkynylation of arenes at room temperature

The rhodium(III)-catalyzed ortho C[BOND]H alkynylation of non-electronically activated arenes is disclosed. This process features a straightforward and highly effective protocol for the synthesis of functionalized alkynes and represents the first example of merging a hypervalent iodine reagent with...

Full description

Bibliographic Details
Main Authors: Feng, Chao, Loh, Teck-Peng
Other Authors: School of Physical and Mathematical Sciences
Format: Journal Article
Language:English
Published: 2014
Subjects:
Online Access:https://hdl.handle.net/10356/100874
http://hdl.handle.net/10220/19640
_version_ 1826123955852804096
author Feng, Chao
Loh, Teck-Peng
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Feng, Chao
Loh, Teck-Peng
author_sort Feng, Chao
collection NTU
description The rhodium(III)-catalyzed ortho C[BOND]H alkynylation of non-electronically activated arenes is disclosed. This process features a straightforward and highly effective protocol for the synthesis of functionalized alkynes and represents the first example of merging a hypervalent iodine reagent with rhodium(III) catalysis. Notably, this reaction proceeds at room temperature, tolerates a variety of functional groups, and more importantly, exhibits high selectivity for monoalkynylation.
first_indexed 2024-10-01T06:12:47Z
format Journal Article
id ntu-10356/100874
institution Nanyang Technological University
language English
last_indexed 2024-10-01T06:12:47Z
publishDate 2014
record_format dspace
spelling ntu-10356/1008742020-03-07T12:34:50Z Rhodium-catalyzed C—H alkynylation of arenes at room temperature Feng, Chao Loh, Teck-Peng School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry The rhodium(III)-catalyzed ortho C[BOND]H alkynylation of non-electronically activated arenes is disclosed. This process features a straightforward and highly effective protocol for the synthesis of functionalized alkynes and represents the first example of merging a hypervalent iodine reagent with rhodium(III) catalysis. Notably, this reaction proceeds at room temperature, tolerates a variety of functional groups, and more importantly, exhibits high selectivity for monoalkynylation. 2014-06-10T08:30:39Z 2019-12-06T20:29:34Z 2014-06-10T08:30:39Z 2019-12-06T20:29:34Z 2014 2014 Journal Article Feng, C., & Loh, T.-P. (2014). Rhodium-Catalyzed C—H Alkynylation of Arenes at Room Temperature. Angewandte Chemie, 126(10), 2760-2764. 0044-8249 https://hdl.handle.net/10356/100874 http://hdl.handle.net/10220/19640 10.1002/ange.201309198 en Angewandte chemie © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
spellingShingle DRNTU::Science::Chemistry::Organic chemistry
Feng, Chao
Loh, Teck-Peng
Rhodium-catalyzed C—H alkynylation of arenes at room temperature
title Rhodium-catalyzed C—H alkynylation of arenes at room temperature
title_full Rhodium-catalyzed C—H alkynylation of arenes at room temperature
title_fullStr Rhodium-catalyzed C—H alkynylation of arenes at room temperature
title_full_unstemmed Rhodium-catalyzed C—H alkynylation of arenes at room temperature
title_short Rhodium-catalyzed C—H alkynylation of arenes at room temperature
title_sort rhodium catalyzed c h alkynylation of arenes at room temperature
topic DRNTU::Science::Chemistry::Organic chemistry
url https://hdl.handle.net/10356/100874
http://hdl.handle.net/10220/19640
work_keys_str_mv AT fengchao rhodiumcatalyzedchalkynylationofarenesatroomtemperature
AT lohteckpeng rhodiumcatalyzedchalkynylationofarenesatroomtemperature